1,139 results on '"Lewis, Sarah J."'
Search Results
2. AI for interpreting screening mammograms: implications for missed cancer in double reading practices and challenging-to-locate lesions
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Jiang, Zhengqiang, Gandomkar, Ziba, Trieu, Phuong Dung (Yun), Taba, Seyedamir Tavakoli, Barron, Melissa L., and Lewis, Sarah J.
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- 2024
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3. Adulthood dietary and lifestyle patterns and risk of breast cancer: Global Cancer Update Programme (CUP Global) systematic literature review
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Konieczna, Jadwiga, Chaplin, Alice, Paz-Graniel, Indira, Croker, Helen, Becerra-Tomás, Nerea, Markozannes, Georgios, Tsilidis, Konstantinos K, Dossus, Laure, Gonzalez-Gil, Esther M, Park, Yikyung, Krebs, John, Weijenberg, Matty P, Baskin, Monica L, Copson, Ellen, Lewis, Sarah J, Seidell, Jacob C, Chowdhury, Rajiv, Hill, Lynette, Chan, Doris SM, and Romaguera, Dora
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- 2025
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4. Exploring the impact of work experience on the detection of specific cancers across different breast density levels on screening mammograms
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Trieu, Phuong Dung (Yun), Barron, Melissa L., Abu Awwad, Dania, and Lewis, Sarah J.
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- 2024
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5. Physical activity, sedentary time and breast cancer risk: a Mendelian randomisation study
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Dixon-Suen, Suzanne C, Lewis, Sarah J, Martin, Richard M, English, Dallas R, Boyle, Terry, Giles, Graham G, Michailidou, Kyriaki, Bolla, Manjeet K, Wang, Qin, Dennis, Joe, Lush, Michael, Investigators, ABCTB, Ahearn, Thomas U, Ambrosone, Christine B, Andrulis, Irene L, Anton-Culver, Hoda, Arndt, Volker, Aronson, Kristan J, Augustinsson, Annelie, Auvinen, Päivi, Freeman, Laura E Beane, Becher, Heiko, Beckmann, Matthias W, Behrens, Sabine, Bermisheva, Marina, Blomqvist, Carl, Bogdanova, Natalia V, Bojesen, Stig E, Bonanni, Bernardo, Brenner, Hermann, Brüning, Thomas, Buys, Saundra S, Camp, Nicola J, Campa, Daniele, Canzian, Federico, Castelao, Jose E, Cessna, Melissa H, Chang-Claude, Jenny, Chanock, Stephen J, Clarke, Christine L, Conroy, Don M, Couch, Fergus J, Cox, Angela, Cross, Simon S, Czene, Kamila, Daly, Mary B, Devilee, Peter, Dörk, Thilo, Dwek, Miriam, Eccles, Diana M, Eliassen, A Heather, Engel, Christoph, Eriksson, Mikael, Evans, D Gareth, Fasching, Peter A, Fletcher, Olivia, Flyger, Henrik, Fritschi, Lin, Gabrielson, Marike, Gago-Dominguez, Manuela, García-Closas, Montserrat, García-Sáenz, José A, Goldberg, Mark S, Guénel, Pascal, Gündert, Melanie, Hahnen, Eric, Haiman, Christopher A, Häberle, Lothar, Håkansson, Niclas, Hall, Per, Hamann, Ute, Hart, Steven N, Harvie, Michelle, Hillemanns, Peter, Hollestelle, Antoinette, Hooning, Maartje J, Hoppe, Reiner, Hopper, John, Howell, Anthony, Hunter, David J, Jakubowska, Anna, Janni, Wolfgang, John, Esther M, Jung, Audrey, Kaaks, Rudolf, Keeman, Renske, Kitahara, Cari M, Koutros, Stella, Kraft, Peter, Kristensen, Vessela N, Kubelka-Sabit, Katerina, Kurian, Allison W, Lacey, James V, Lambrechts, Diether, Le Marchand, Loic, Lindblom, Annika, Loibl, Sibylle, Lubiński, Jan, Mannermaa, Arto, and Manoochehri, Mehdi
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Biomedical and Clinical Sciences ,Health Services and Systems ,Health Sciences ,Public Health ,Oncology and Carcinogenesis ,Cancer ,Behavioral and Social Science ,Women's Health ,Genetics ,Breast Cancer ,Prevention ,Obesity ,Physical Activity ,Female ,Humans ,Breast Neoplasms ,Exercise ,Mendelian Randomization Analysis ,Polymorphism ,Single Nucleotide ,Risk Factors ,Sedentary Behavior ,Breast Cancer Association Consortium ,Breast ,Physical activity ,Sedentary Behaviour ,Engineering ,Medical and Health Sciences ,Education ,Sport Sciences ,Clinical sciences ,Sports science and exercise ,Applied and developmental psychology - Abstract
ObjectivesPhysical inactivity and sedentary behaviour are associated with higher breast cancer risk in observational studies, but ascribing causality is difficult. Mendelian randomisation (MR) assesses causality by simulating randomised trial groups using genotype. We assessed whether lifelong physical activity or sedentary time, assessed using genotype, may be causally associated with breast cancer risk overall, pre/post-menopause, and by case-groups defined by tumour characteristics.MethodsWe performed two-sample inverse-variance-weighted MR using individual-level Breast Cancer Association Consortium case-control data from 130 957 European-ancestry women (69 838 invasive cases), and published UK Biobank data (n=91 105-377 234). Genetic instruments were single nucleotide polymorphisms (SNPs) associated in UK Biobank with wrist-worn accelerometer-measured overall physical activity (nsnps=5) or sedentary time (nsnps=6), or accelerometer-measured (nsnps=1) or self-reported (nsnps=5) vigorous physical activity.ResultsGreater genetically-predicted overall activity was associated with lower breast cancer overall risk (OR=0.59; 95% confidence interval (CI) 0.42 to 0.83 per-standard deviation (SD;~8 milligravities acceleration)) and for most case-groups. Genetically-predicted vigorous activity was associated with lower risk of pre/perimenopausal breast cancer (OR=0.62; 95% CI 0.45 to 0.87,≥3 vs. 0 self-reported days/week), with consistent estimates for most case-groups. Greater genetically-predicted sedentary time was associated with higher hormone-receptor-negative tumour risk (OR=1.77; 95% CI 1.07 to 2.92 per-SD (~7% time spent sedentary)), with elevated estimates for most case-groups. Results were robust to sensitivity analyses examining pleiotropy (including weighted-median-MR, MR-Egger).ConclusionOur study provides strong evidence that greater overall physical activity, greater vigorous activity, and lower sedentary time are likely to reduce breast cancer risk. More widespread adoption of active lifestyles may reduce the burden from the most common cancer in women.
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- 2022
6. Optimizing Radiological Education: The Role of Learning Spacing via Test sets in Enhancing Diagnostic Proficiency in Breast Screening Readers
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Trieu, Phuong Dung (Yun), Abu Awwad, Dania, Barron, Melissa L., and Lewis, Sarah J.
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- 2024
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7. Global Radiomic Features from Mammography for Predicting Difficult-To-Interpret Normal Cases
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Siviengphanom, Somphone, Gandomkar, Ziba, Lewis, Sarah J., and Brennan, Patrick C.
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- 2023
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8. Genetically proxied glucose-lowering drug target perturbation and risk of cancer: a Mendelian randomisation analysis
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Yarmolinsky, James, Bouras, Emmanouil, Constantinescu, Andrei, Burrows, Kimberley, Bull, Caroline J., Vincent, Emma E., Martin, Richard M., Dimopoulou, Olympia, Lewis, Sarah J., Moreno, Victor, Vujkovic, Marijana, Chang, Kyong-Mi, Voight, Benjamin F., Tsao, Philip S., Gunter, Marc J., Hampe, Jochen, Pellatt, Andrew J., Pharoah, Paul D. P., Schoen, Robert E., Gallinger, Steven, Jenkins, Mark A., Pai, Rish K., Gill, Dipender, and Tsilidis, Kostas K.
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- 2023
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9. Environmental and genetic predictors of whole blood mercury and selenium concentrations in pregnant women in a UK birth cohort
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Dack, Kyle, Huang, Peiyuan, Taylor, Caroline M, Rai, Dheeraj, and Lewis, Sarah J
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- 2024
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10. Infection prevention and control in computed tomography: creating a national survey
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Hill, Suzanne, Jimenez, Yobelli A., Abu Awwad, Dania, and Lewis, Sarah J.
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- 2024
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11. Association between circulating inflammatory markers and adult cancer risk: a Mendelian randomization analysis
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Landi, Maria Teresa, Stevens, Victoria, Wang, Ying, Albanes, Demetrios, Caporaso, Neil, Brennan, Paul, Amos, Christopher I., Shete, Sanjay, Hung, Rayjean J., Bickeböller, Heike, Risch, Angela, Houlston, Richard, Lam, Stephen, Tardon, Adonina, Chen, Chu, Bojesen, Stig E., Johansson, Mattias, Wichmann, H-Erich, Christiani, David, Rennert, Gadi, Arnold, Susanne, Field, John K., Le Marchand, Loic, Melander, Olle, Brunnström, Hans, Liu, Geoffrey, Andrew, Angeline, Kiemeney, Lambertus A., Shen, Hongbing, Zienolddiny, Shan, Grankvist, Kjell, Johansson, Mikael, Teare, M. Dawn, Hong, Yun-Chul, Yuan, Jian-Min, Lazarus, Philip, Schabath, Matthew B., Aldrich, Melinda C., Eeles, Rosalind A., Haiman, Christopher A., Kote-Jarai, Zsofia, Schumacher, Fredrick R., Benlloch, Sara, Al Olama, Ali Amin, Muir, Kenneth R., Berndt, Sonja I., Conti, David V., Wiklund, Fredrik, Chanock, Stephen, Tangen, Catherine M., Batra, Jyotsna, Clements, Judith A., Grönberg, Henrik, Pashayan, Nora, Schleutker, Johanna, Albanes, Demetrius, Weinstein, Stephanie J., Wolk, Alicja, West, Catharine M.L., Mucci, Lorelei A., Cancel-Tassin, Géraldine, Koutros, Stella, Sørensen, Karina Dalsgaard, Grindedal, Eli Marie, Neal, David E., Hamdy, Freddie C., Donovan, Jenny L., Travis, Ruth C., Hamilton, Robert J., Ingles, Sue Ann, Rosenstein, Barry S., Lu, Yong-Jie, Giles, Graham G., MacInnis, Robert J., Kibel, Adam S., Vega, Ana, Kogevinas, Manolis, Penney, Kathryn L., Park, Jong Y., Stanfrod, Janet L., Cybulski, Cezary, Nordestgaard, Børge G., Nielsen, Sune F., Brenner, Hermann, Maier, Christiane, Logothetis, Christopher J., John, Esther M., Teixeira, Manuel R., Neuhausen, Susan L., De Ruyck, Kim, Razack, Azad, Newcomb, Lisa F., Lessel, Davor, Kaneva, Radka, Usmani, Nawaid, Claessens, Frank, Townsend, Paul A., Castelao, Jose Esteban, Roobol, Monique J., Menegaux, Florence, Khaw, Kay-Tee, Cannon-Albright, Lisa, Pandha, Hardev, Thibodeau, Stephen N., Hunter, David J., Kraft, Peter, Blot, William J., Riboli, Elio, Yarmolinsky, James, Robinson, Jamie W., Mariosa, Daniela, Karhunen, Ville, Huang, Jian, Dimou, Niki, Murphy, Neil, Burrows, Kimberley, Bouras, Emmanouil, Smith-Byrne, Karl, Lewis, Sarah J., Galesloot, Tessel E., Vermeulen, Sita, Martin, Paul, Hou, Lifang, Newcomb, Polly A., White, Emily, Wu, Anna H., Le Marchand, Loïc, Phipps, Amanda I., Buchanan, Daniel D., Zhao, Sizheng Steven, Gill, Dipender, Chanock, Stephen J., Purdue, Mark P., Davey Smith, George, Herzig, Karl-Heinz, Järvelin, Marjo-Riitta, Amos, Chris I., Dehghan, Abbas, Gunter, Marc J., Tsilidis, Kostas K., and Martin, Richard M.
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- 2024
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12. Blood pressure, calcium channel blockers, and the risk of prostate cancer: a Mendelian randomization study
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Kazmi, Nabila, Valeeva, Elena V., Khasanova, Gulshat R., Lewis, Sarah J., and Plotnikov, Denis
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- 2023
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13. Infection prevention and control in the medical imaging environment: a scoping review
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Jimenez, Yobelli A. and Lewis, Sarah J.
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- 2023
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14. Genetically predicted circulating concentrations of micronutrients and risk of colorectal cancer among individuals of European descent: a Mendelian randomization study
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Tsilidis, Konstantinos K, Papadimitriou, Nikos, Dimou, Niki, Gill, Dipender, Lewis, Sarah J, Martin, Richard M, Murphy, Neil, Markozannes, Georgios, Zuber, Verena, Cross, Amanda J, Burrows, Kimberley, Lopez, David S, Key, Timothy J, Travis, Ruth C, Perez-Cornago, Aurora, Hunter, David J, van Duijnhoven, Fränzel JB, Albanes, Demetrius, Arndt, Volker, Berndt, Sonja I, Bézieau, Stéphane, Bishop, D Timothy, Boehm, Juergen, Brenner, Hermann, Burnett-Hartman, Andrea, Campbell, Peter T, Casey, Graham, Castellví-Bel, Sergi, Chan, Andrew T, Chang-Claude, Jenny, de la Chapelle, Albert, Figueiredo, Jane C, Gallinger, Steven J, Giles, Graham G, Goodman, Phyllis J, Gsur, Andrea, Hampe, Jochen, Hampel, Heather, Hoffmeister, Michael, Jenkins, Mark A, Keku, Temitope O, Kweon, Sun-Seog, Larsson, Susanna C, Le Marchand, Loic, Li, Christopher I, Li, Li, Lindblom, Annika, Martín, Vicente, Milne, Roger L, Moreno, Victor, Nan, Hongmei, Nassir, Rami, Newcomb, Polly A, Offit, Kenneth, Pharoah, Paul DP, Platz, Elizabeth A, Potter, John D, Qi, Lihong, Rennert, Gad, Sakoda, Lori C, Schafmayer, Clemens, Slattery, Martha L, Snetselaar, Linda, Schenk, Jeanette, Thibodeau, Stephen N, Ulrich, Cornelia M, Van Guelpen, Bethany, Harlid, Sophia, Visvanathan, Kala, Vodickova, Ludmila, Wang, Hansong, White, Emily, Wolk, Alicja, Woods, Michael O, Wu, Anna H, Zheng, Wei, Bueno-de-Mesquita, Bas, Boutron-Ruault, Marie-Christine, Hughes, David J, Jakszyn, Paula, Kühn, Tilman, Palli, Domenico, Riboli, Elio, Giovannucci, Edward L, Banbury, Barbara L, Gruber, Stephen B, Peters, Ulrike, Gunter, Marc J, and on behalf of GECCO, CORECT
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Complementary and Integrative Health ,Digestive Diseases ,Clinical Research ,Clinical Trials and Supportive Activities ,Cancer ,Colo-Rectal Cancer ,Prevention ,Nutrition ,Prevention of disease and conditions ,and promotion of well-being ,3.3 Nutrition and chemoprevention ,Case-Control Studies ,Colorectal Neoplasms ,Dietary Supplements ,Genetic Predisposition to Disease ,Humans ,Mendelian Randomization Analysis ,Micronutrients ,Risk Factors ,Selenium ,Vitamin B 12 ,White People ,Mendelian randomization ,genes ,nutrition ,supplements ,colorectal cancer ,Engineering ,Medical and Health Sciences ,Nutrition & Dietetics - Abstract
BackgroundThe literature on associations of circulating concentrations of minerals and vitamins with risk of colorectal cancer is limited and inconsistent. Evidence from randomized controlled trials (RCTs) to support the efficacy of dietary modification or nutrient supplementation for colorectal cancer prevention is also limited.ObjectivesTo complement observational and RCT findings, we investigated associations of genetically predicted concentrations of 11 micronutrients (β-carotene, calcium, copper, folate, iron, magnesium, phosphorus, selenium, vitamin B-6, vitamin B-12, and zinc) with colorectal cancer risk using Mendelian randomization (MR).MethodsTwo-sample MR was conducted using 58,221 individuals with colorectal cancer and 67,694 controls from the Genetics and Epidemiology of Colorectal Cancer Consortium, Colorectal Cancer Transdisciplinary Study, and Colon Cancer Family Registry. Inverse variance-weighted MR analyses were performed with sensitivity analyses to assess the impact of potential violations of MR assumptions.ResultsNominally significant associations were noted for genetically predicted iron concentration and higher risk of colon cancer [ORs per SD (ORSD): 1.08; 95% CI: 1.00, 1.17; P value = 0.05] and similarly for proximal colon cancer, and for vitamin B-12 concentration and higher risk of colorectal cancer (ORSD: 1.12; 95% CI: 1.03, 1.21; P value = 0.01) and similarly for colon cancer. A nominally significant association was also noted for genetically predicted selenium concentration and lower risk of colon cancer (ORSD: 0.98; 95% CI: 0.96, 1.00; P value = 0.05) and similarly for distal colon cancer. These associations were robust to sensitivity analyses. Nominally significant inverse associations were observed for zinc and risk of colorectal and distal colon cancers, but sensitivity analyses could not be performed. None of these findings survived correction for multiple testing. Genetically predicted concentrations of β-carotene, calcium, copper, folate, magnesium, phosphorus, and vitamin B-6 were not associated with disease risk.ConclusionsThese results suggest possible causal associations of circulating iron and vitamin B-12 (positively) and selenium (inversely) with risk of colon cancer.
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- 2021
15. Radiologist Self-training: a Study of Cancer Detection when Reading Mammograms at Work Clinics or Workshops
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Lewis, Sarah J., Borecky, Natacha, Li, Tong, Barron, Melissa L., Brennan, Patrick, and Trieu, Phuong Dung Yun
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- 2023
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16. Use of Full-quality DICOM Images Compared to Minimally Compressed Mammograms in JPEG Format for Radiology Training: A Study From Radiologist and Radiographer Perspectives
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Trieu, Phuong Dung (Yun), Barron, Melissa, and Lewis, Sarah J.
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- 2023
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17. Infection prevention and control in medical imaging surveys: The need to map to guidelines to address systemic issues?
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Jimenez, Yobelli A., Hill, Suzanne, and Lewis, Sarah J.
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- 2023
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18. Does testosterone mediate the relationship between vitamin D and prostate cancer progression? A systematic review and meta-analysis
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Robles, Luke A., Harrison, Sean, Tan, Vanessa Y., Beynon, Rhona, McAleenan, Alexandra, Higgins, Julian PT., Martin, Richard M., and Lewis, Sarah J.
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- 2022
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19. Mammography-based Radiomics in Breast Cancer: A Scoping Review of Current Knowledge and Future Needs
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Siviengphanom, Somphone, Gandomkar, Ziba, Lewis, Sarah J., and Brennan, Patrick C.
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- 2022
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20. A machine learning model based on readers’ characteristics to predict their performances in reading screening mammograms
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Gandomkar, Ziba, Lewis, Sarah J., Li, Tong, Ekpo, Ernest U., and Brennan, Patrick C.
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- 2022
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21. Applying Mendelian randomization to appraise causality in relationships between nutrition and cancer
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Wade, Kaitlin H., Yarmolinsky, James, Giovannucci, Edward, Lewis, Sarah J., Millwood, Iona Y., Munafò, Marcus R., Meddens, Fleur, Burrows, Kimberley, Bell, Joshua A., Davies, Neil M., Mariosa, Daniela, Kanerva, Noora, Vincent, Emma E., Smith-Byrne, Karl, Guida, Florence, Gunter, Marc J., Sanderson, Eleanor, Dudbridge, Frank, Burgess, Stephen, Cornelis, Marilyn C., Richardson, Tom G., Borges, Maria Carolina, Bowden, Jack, Hemani, Gibran, Cho, Yoonsu, Spiller, Wes, Richmond, Rebecca C., Carter, Alice R., Langdon, Ryan, Lawlor, Deborah A., Walters, Robin G., Vimaleswaran, Karani Santhanakrishnan, Anderson, Annie, Sandu, Meda R., Tilling, Kate, Davey Smith, George, Martin, Richard M., and Relton, Caroline L.
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- 2022
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22. Predicting Syndromic Status Based on Longitudinal Data from Parental Reports of the Presence of Additional Structural and Functional Anomalies in Children Born with an Orofacial Cleft.
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Davies, Amy J. V., Wren, Yvonne E., Hamilton, Mark, Sandy, Jonathan R., Stergiakouli, Evangelia, and Lewis, Sarah J.
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CLEFT lip ,CLEFT palate ,SECONDARY analysis ,HUMAN abnormalities ,GENETIC counseling - Abstract
Background: Orofacial clefts are the most common craniofacial congenital malformation in humans. Approximately 30% of clefts arise as part of a syndrome or sequence, characterised by co-existing structural and functional anomalies. Many syndromes are thought to be undiagnosed, although the presence of multiple anomalies may indicate the presence of a syndrome or sequence. Aim: To determine the extent to which the presence of additional structural and functional anomalies can help to identify those children with an undiagnosed syndrome. Methods: Secondary data analysis was performed using data from 1701 children born with an orofacial cleft, collected as part of a longitudinal cohort study, the Cleft Collective. Data were collected between 2013 and 2023 across the United Kingdom. The prevalence of structural and functional anomalies and syndromes were explored using descriptive statistics. Logistic regression was used to determine the extent to which anomalies can predict syndromic status. Results: A syndrome and/or sequence was reported in 20.5% children. Among children who reported five or more anomalies, the prevalence of a diagnosed syndrome was 81.5%. When adjusting for cleft subtype and sex, in 27 out of 32 anomalies tested, strong evidence was found to suggest increased odds of having a syndrome if the specific anomaly was present compared to if the anomaly was absent (p-values ranged between 1.4 × 10
−30 and 0.002). Conclusions: Children born with a cleft who present with two or more anomalies are much more likely to have a syndrome than those with fewer anomalies and should be prioritised for genetic screening and counselling. [ABSTRACT FROM AUTHOR]- Published
- 2024
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23. Micronutrients and Major Depression: A Mendelian Randomisation Study.
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Carnegie, Rebecca E., Zheng, Jie, Borges, Maria C., Jones, Hannah J., Wade, Kaitlin H., Sallis, Hannah M., Lewis, Sarah J., Evans, David M., Revez, Joana A., Evans, Jonathan, and Martin, Richard M.
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Background: Various vitamins and minerals have been implicated in the aetiology of depression. Objective: To estimate the effects of micronutrient exposures on major depressive disorder (MDD) and recurrent depression (rMDD) using Mendelian randomisation (MR), a method using genetic data to estimate causal effects given certain assumptions. Methods: We undertook a comprehensive bidirectional MR study of multiple micronutrient exposures on MDD and rMDD. Summary statistics were obtained from the Psychiatric Genomics Consortium (PGC) genome-wide association studies (GWASs) of MDD (cases = 116,209; controls = 314,566) and rMDD (cases = 17,451; controls = 62,482). Results: None of the micronutrients with available genetic instruments were strongly associated with MDD or rMDD using traditional MR methods. However, using methods to increase analytical power by accounting for genetically correlated variants (e.g., cIVW) highlighted five micronutrients with possible causal effects. Point estimates for rMDD were the largest magnitude, with three micronutrients suggestive of a protective effect: serum iron (OR
cIVW 0.90 per SD increase; 95% CI 0.85–0.95; p = 0.0003); erythrocyte copper (ORcIVW 0.97; 95% CI 0.95–0.99; p = 0.0004); and 25(OH) vitamin D (ORcIVW 0.81; 0.66–0.99; p = 0.04). Apparent adverse effects of increased selenium on the risk of MDD (ORcIVW 1.03; 95% CI 1.02–1.05; p = 0.0003) and rMDD (ORcIVW 1.08; 95% CI 1.00–1.08; p = 0.06), and serum magnesium on rMDD (ORcIVW 1.21; 1.01–1.44; p = 0.04); were less consistent between methods and may be driven by pleiotropy. Conclusions: Our results suggest weak evidence for a protective effect of iron, copper and 25(OH)D on major depressive outcomes, with mixed evidence for selenium and magnesium. There was no evidence to support a causal effect of any other micronutrients on MDD or rMDD, although genetic instruments were lacking, with insufficient power to detect small but important effects. Future micronutrient supplementation trials should ensure ample statistical power given modest causal effect estimates and consider potential risks of supplementation, as some micronutrient effect estimates suggested potential harm in excess. [ABSTRACT FROM AUTHOR]- Published
- 2024
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24. Circulating inflammatory cytokines and risk of five cancers: a Mendelian randomization analysis
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Bouras, Emmanouil, Karhunen, Ville, Gill, Dipender, Huang, Jian, Haycock, Philip C., Gunter, Marc J., Johansson, Mattias, Brennan, Paul, Key, Tim, Lewis, Sarah J., Martin, Richard M., Murphy, Neil, Platz, Elizabeth A., Travis, Ruth, Yarmolinsky, James, Zuber, Verena, Martin, Paul, Katsoulis, Michail, Freisling, Heinz, Nøst, Therese Haugdahl, Schulze, Matthias B., Dossus, Laure, Hung, Rayjean J., Amos, Christopher I., Ahola-Olli, Ari, Palaniswamy, Saranya, Männikkö, Minna, Auvinen, Juha, Herzig, Karl-Heinz, Keinänen-Kiukaanniemi, Sirkka, Lehtimäki, Terho, Salomaa, Veikko, Raitakari, Olli, Salmi, Marko, Jalkanen, Sirpa, Jarvelin, Marjo-Riitta, Dehghan, Abbas, and Tsilidis, Konstantinos K.
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- 2022
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25. Associations between plasma fatty acid concentrations and schizophrenia: a two-sample Mendelian randomisation study
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Jones, Hannah J, Borges, Maria Carolina, Carnegie, Rebecca, Mongan, David, Rogers, Peter J, Lewis, Sarah J, Thompson, Andrew D, and Zammit, Stanley
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- 2021
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26. Allergy, asthma, and the risk of breast and prostate cancer : a Mendelian randomization study
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Jiang, Xia, Dimou, Niki L., Zhu, Zhaozhong, Bonilla, Carolina, Lewis, Sarah J., Lindström, Sara, Kraft, Peter, Tsilidis, Konstantinos K., and Martin, Richard M.
- Published
- 2020
27. Student Perceptions of Remote Access Simulated Learning in Computed Tomography
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Liley, Tara, Ryan, Elaine, Lee, Kristal, Dimmock, Matthew, Robinson, John, and Lewis, Sarah J.
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National professional capabilities for Australian Diagnostic Radiography (DR) graduates require computed tomography (CT) scanning competence. Clinical placements have varied success in achiveing CT learning experiences and dedicated simulation at university can aid development of clinical skills. This study explored DR undergraduate students' attitudes, confidence and experiences of using a remote access simulation facility equipped with a live radiation commercial scanner. A pre- and post-clinical placement survey, with Likert scales and open-ended questions, was employed. Students in their third year of study undertook formal simulation CT learning using the NETRAD CT facility, prior to a four week off-campus clinical placement. Results indicate students (pre n = 21; post n = 23) had mixed levels of satisfaction when using NETRAD CT even though learning outcomes and relevance was clear. Comparison of pre- and post-matched statements reveals a significant decrease in students' perception of confidence in their skills post-clinical placement, reduced satisfaction with remote learning and increased preference for hands-on experiences. Open-ended responses were polarised to either positive simulation themes of convenience and repeatability, alongside negative themes with remote access and lack of facilitation. While students considered CT simulation to be educationally engaging, the technology-rich learning environment presented challenges and believed interactive simulation is inferior to real clinical experiences.
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- 2020
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28. Identification of potential mediators of the relationship between body mass index and colorectal cancer: a Mendelian randomization analysis
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Bouras, Emmanouil, primary, Gill, Dipender, additional, Zuber, Verena, additional, Murphy, Neil, additional, Dimou, Niki, additional, Aleksandrova, Krasimira, additional, Lewis, Sarah J, additional, Martin, Richard M, additional, Yarmolinsky, James, additional, Albanes, Demetrius, additional, Brenner, Hermann, additional, Castellví-Bel, Sergi, additional, Chan, Andrew T, additional, Cheng, Iona, additional, Gruber, Stephen, additional, Van Guelpen, Bethany, additional, Li, Christopher I, additional, Le Marchand, Loic, additional, Newcomb, Polly A, additional, Ogino, Shuji, additional, Pellatt, Andrew, additional, Schmit, Stephanie L, additional, Wolk, Alicja, additional, Wu, Anna H, additional, Peters, Ulrike, additional, Gunter, Marc J, additional, and Tsilidis, Konstantinos K, additional
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- 2024
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29. Artificial intelligence can improve cancer detection in a double reading screening mammography scenario
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Jiang, Zhengqiang, primary, Gandomkar, Ziba, additional, Trieu, Phuong D., additional, Tavakoli Taba, Seyedamir, additional, Barron, Melissa L., additional, and Lewis, Sarah J., additional
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- 2024
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30. Association between circulating inflammatory markers and adult cancer risk: a Mendelian randomization analysis
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Yarmolinsky, James, primary, Robinson, Jamie W., additional, Mariosa, Daniela, additional, Karhunen, Ville, additional, Huang, Jian, additional, Dimou, Niki, additional, Murphy, Neil, additional, Burrows, Kimberley, additional, Bouras, Emmanouil, additional, Smith-Byrne, Karl, additional, Lewis, Sarah J., additional, Galesloot, Tessel E., additional, Kiemeney, Lambertus A., additional, Vermeulen, Sita, additional, Martin, Paul, additional, Albanes, Demetrius, additional, Hou, Lifang, additional, Newcomb, Polly A., additional, White, Emily, additional, Wolk, Alicja, additional, Wu, Anna H., additional, Le Marchand, Loïc, additional, Phipps, Amanda I., additional, Buchanan, Daniel D., additional, Zhao, Sizheng Steven, additional, Gill, Dipender, additional, Chanock, Stephen J., additional, Purdue, Mark P., additional, Davey Smith, George, additional, Brennan, Paul, additional, Herzig, Karl-Heinz, additional, Järvelin, Marjo-Riitta, additional, Amos, Chris I., additional, Hung, Rayjean J., additional, Dehghan, Abbas, additional, Johansson, Mattias, additional, Gunter, Marc J., additional, Tsilidis, Kostas K., additional, Martin, Richard M., additional, Landi, Maria Teresa, additional, Stevens, Victoria, additional, Wang, Ying, additional, Albanes, Demetrios, additional, Caporaso, Neil, additional, Amos, Christopher I., additional, Shete, Sanjay, additional, Bickeböller, Heike, additional, Risch, Angela, additional, Houlston, Richard, additional, Lam, Stephen, additional, Tardon, Adonina, additional, Chen, Chu, additional, Bojesen, Stig E., additional, Wichmann, H-Erich, additional, Christiani, David, additional, Rennert, Gadi, additional, Arnold, Susanne, additional, Field, John K., additional, Le Marchand, Loic, additional, Melander, Olle, additional, Brunnström, Hans, additional, Liu, Geoffrey, additional, Andrew, Angeline, additional, Shen, Hongbing, additional, Zienolddiny, Shan, additional, Grankvist, Kjell, additional, Johansson, Mikael, additional, Teare, M. Dawn, additional, Hong, Yun-Chul, additional, Yuan, Jian-Min, additional, Lazarus, Philip, additional, Schabath, Matthew B., additional, Aldrich, Melinda C., additional, Eeles, Rosalind A., additional, Haiman, Christopher A., additional, Kote-Jarai, Zsofia, additional, Schumacher, Fredrick R., additional, Benlloch, Sara, additional, Al Olama, Ali Amin, additional, Muir, Kenneth R., additional, Berndt, Sonja I., additional, Conti, David V., additional, Wiklund, Fredrik, additional, Chanock, Stephen, additional, Tangen, Catherine M., additional, Batra, Jyotsna, additional, Clements, Judith A., additional, Grönberg, Henrik, additional, Pashayan, Nora, additional, Schleutker, Johanna, additional, Weinstein, Stephanie J., additional, West, Catharine M.L., additional, Mucci, Lorelei A., additional, Cancel-Tassin, Géraldine, additional, Koutros, Stella, additional, Sørensen, Karina Dalsgaard, additional, Grindedal, Eli Marie, additional, Neal, David E., additional, Hamdy, Freddie C., additional, Donovan, Jenny L., additional, Travis, Ruth C., additional, Hamilton, Robert J., additional, Ingles, Sue Ann, additional, Rosenstein, Barry S., additional, Lu, Yong-Jie, additional, Giles, Graham G., additional, MacInnis, Robert J., additional, Kibel, Adam S., additional, Vega, Ana, additional, Kogevinas, Manolis, additional, Penney, Kathryn L., additional, Park, Jong Y., additional, Stanfrod, Janet L., additional, Cybulski, Cezary, additional, Nordestgaard, Børge G., additional, Nielsen, Sune F., additional, Brenner, Hermann, additional, Maier, Christiane, additional, Logothetis, Christopher J., additional, John, Esther M., additional, Teixeira, Manuel R., additional, Neuhausen, Susan L., additional, De Ruyck, Kim, additional, Razack, Azad, additional, Newcomb, Lisa F., additional, Lessel, Davor, additional, Kaneva, Radka, additional, Usmani, Nawaid, additional, Claessens, Frank, additional, Townsend, Paul A., additional, Castelao, Jose Esteban, additional, Roobol, Monique J., additional, Menegaux, Florence, additional, Khaw, Kay-Tee, additional, Cannon-Albright, Lisa, additional, Pandha, Hardev, additional, Thibodeau, Stephen N., additional, Hunter, David J., additional, Kraft, Peter, additional, Blot, William J., additional, and Riboli, Elio, additional
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- 2024
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31. Post-diagnosis physical activity and sedentary behaviour and colorectal cancer prognosis: A Global Cancer Update Programme (CUP Global) systematic literature review and meta-analysis
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Epi Kanker, Cancer, JC onderzoeksprogramma Cancer, Markozannes, Georgios, Becerra-Tomás, Nerea, Cariolou, Margarita, Balducci, Katia, Vieira, Rita, Kiss, Sonia, Aune, Dagfinn, Greenwood, Darren C, Gunter, Marc J, Copson, Ellen, Renehan, Andrew G, Bours, Martijn, Demark-Wahnefried, Wendy, Hudson, Melissa M, May, Anne M, Odedina, Folakemi T, Skinner, Roderick, Steindorf, Karen, Tjønneland, Anne, Velikova, Galina, Baskin, Monica L, Chowdhury, Rajiv, Hill, Lynette, Lewis, Sarah J, Seidell, Jaap, Weijenberg, Matty P, Krebs, John, Cross, Amanda J, Tsilidis, Konstantinos K, Chan, Doris S M, Epi Kanker, Cancer, JC onderzoeksprogramma Cancer, Markozannes, Georgios, Becerra-Tomás, Nerea, Cariolou, Margarita, Balducci, Katia, Vieira, Rita, Kiss, Sonia, Aune, Dagfinn, Greenwood, Darren C, Gunter, Marc J, Copson, Ellen, Renehan, Andrew G, Bours, Martijn, Demark-Wahnefried, Wendy, Hudson, Melissa M, May, Anne M, Odedina, Folakemi T, Skinner, Roderick, Steindorf, Karen, Tjønneland, Anne, Velikova, Galina, Baskin, Monica L, Chowdhury, Rajiv, Hill, Lynette, Lewis, Sarah J, Seidell, Jaap, Weijenberg, Matty P, Krebs, John, Cross, Amanda J, Tsilidis, Konstantinos K, and Chan, Doris S M
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- 2024
32. Post-diagnosis adiposity and colorectal cancer prognosis: A Global Cancer Update Programme (CUP Global) systematic literature review and meta-analysis
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Epi Kanker, Cancer, JC onderzoeksprogramma Kanker, Becerra-Tomás, Nerea, Markozannes, Georgios, Cariolou, Margarita, Balducci, Katia, Vieira, Rita, Kiss, Sonia, Aune, Dagfinn, Greenwood, Darren C, Dossus, Laure, Copson, Ellen, Renehan, Andrew G, Bours, Martijn, Demark-Wahnefried, Wendy, Hudson, Melissa M, May, Anne M, Odedina, Folakemi T, Skinner, Roderick, Steindorf, Karen, Tjønneland, Anne, Velikova, Galina, Baskin, Monica L, Chowdhury, Rajiv, Hill, Lynette, Lewis, Sarah J, Seidell, Jaap, Weijenberg, Matty P, Krebs, John, Cross, Amanda J, Tsilidis, Konstantinos K, Chan, Doris S M, Epi Kanker, Cancer, JC onderzoeksprogramma Kanker, Becerra-Tomás, Nerea, Markozannes, Georgios, Cariolou, Margarita, Balducci, Katia, Vieira, Rita, Kiss, Sonia, Aune, Dagfinn, Greenwood, Darren C, Dossus, Laure, Copson, Ellen, Renehan, Andrew G, Bours, Martijn, Demark-Wahnefried, Wendy, Hudson, Melissa M, May, Anne M, Odedina, Folakemi T, Skinner, Roderick, Steindorf, Karen, Tjønneland, Anne, Velikova, Galina, Baskin, Monica L, Chowdhury, Rajiv, Hill, Lynette, Lewis, Sarah J, Seidell, Jaap, Weijenberg, Matty P, Krebs, John, Cross, Amanda J, Tsilidis, Konstantinos K, and Chan, Doris S M
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- 2024
33. Post-diagnosis adiposity, physical activity, sedentary behaviour, dietary factors, supplement use and colorectal cancer prognosis: Global Cancer Update Programme (CUP Global) summary of evidence grading
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Epi Kanker, Cancer, JC onderzoeksprogramma Cancer, Tsilidis, Konstantinos K, Markozannes, Georgios, Becerra-Tomás, Nerea, Cariolou, Margarita, Balducci, Katia, Vieira, Rita, Kiss, Sonia, Aune, Dagfinn, Greenwood, Darren C, Dossus, Laure, González-Gil, Esther M, Gunter, Marc J, Allen, Kate, Brockton, Nigel T, Croker, Helen, Gordon-Dseagu, Vanessa L, Mitrou, Panagiota, Musuwo, Nicole, Wiseman, Martin J, Copson, Ellen, Renehan, Andrew G, Bours, Martijn, Demark-Wahnefried, Wendy, Hudson, Melissa M, May, Anne M, Odedina, Folakemi T, Skinner, Roderick, Steindorf, Karen, Tjønneland, Anne, Velikova, Galina, Baskin, Monica L, Chowdhury, Rajiv, Hill, Lynette, Lewis, Sarah J, Seidell, Jaap, Weijenberg, Matty P, Krebs, John, Cross, Amanda J, Chan, Doris S M, Epi Kanker, Cancer, JC onderzoeksprogramma Cancer, Tsilidis, Konstantinos K, Markozannes, Georgios, Becerra-Tomás, Nerea, Cariolou, Margarita, Balducci, Katia, Vieira, Rita, Kiss, Sonia, Aune, Dagfinn, Greenwood, Darren C, Dossus, Laure, González-Gil, Esther M, Gunter, Marc J, Allen, Kate, Brockton, Nigel T, Croker, Helen, Gordon-Dseagu, Vanessa L, Mitrou, Panagiota, Musuwo, Nicole, Wiseman, Martin J, Copson, Ellen, Renehan, Andrew G, Bours, Martijn, Demark-Wahnefried, Wendy, Hudson, Melissa M, May, Anne M, Odedina, Folakemi T, Skinner, Roderick, Steindorf, Karen, Tjønneland, Anne, Velikova, Galina, Baskin, Monica L, Chowdhury, Rajiv, Hill, Lynette, Lewis, Sarah J, Seidell, Jaap, Weijenberg, Matty P, Krebs, John, Cross, Amanda J, and Chan, Doris S M
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- 2024
34. Post-diagnosis dietary factors, supplement use and colorectal cancer prognosis: A Global Cancer Update Programme (CUP Global) systematic literature review and meta-analysis
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Epi Kanker, Cancer, JC onderzoeksprogramma Kanker, Chan, Doris S M, Cariolou, Margarita, Markozannes, Georgios, Balducci, Katia, Vieira, Rita, Kiss, Sonia, Becerra-Tomás, Nerea, Aune, Dagfinn, Greenwood, Darren C, González-Gil, Esther M, Copson, Ellen, Renehan, Andrew G, Bours, Martijn, Demark-Wahnefried, Wendy, Hudson, Melissa M, May, Anne M, Odedina, Folakemi T, Skinner, Roderick, Steindorf, Karen, Tjønneland, Anne, Velikova, Galina, Baskin, Monica L, Chowdhury, Rajiv, Hill, Lynette, Lewis, Sarah J, Seidell, Jaap, Weijenberg, Matty P, Krebs, John, Cross, Amanda J, Tsilidis, Konstantinos K, Epi Kanker, Cancer, JC onderzoeksprogramma Kanker, Chan, Doris S M, Cariolou, Margarita, Markozannes, Georgios, Balducci, Katia, Vieira, Rita, Kiss, Sonia, Becerra-Tomás, Nerea, Aune, Dagfinn, Greenwood, Darren C, González-Gil, Esther M, Copson, Ellen, Renehan, Andrew G, Bours, Martijn, Demark-Wahnefried, Wendy, Hudson, Melissa M, May, Anne M, Odedina, Folakemi T, Skinner, Roderick, Steindorf, Karen, Tjønneland, Anne, Velikova, Galina, Baskin, Monica L, Chowdhury, Rajiv, Hill, Lynette, Lewis, Sarah J, Seidell, Jaap, Weijenberg, Matty P, Krebs, John, Cross, Amanda J, and Tsilidis, Konstantinos K
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- 2024
35. Identification of potential mediators of the relationship between body mass index and colorectal cancer : a Mendelian randomization analysis
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Bouras, Emmanouil, Gill, Dipender, Zuber, Verena, Murphy, Neil, Dimou, Niki, Aleksandrova, Krasimira, Lewis, Sarah J., Martin, Richard M., Yarmolinsky, James, Albanes, Demetrius, Brenner, Hermann, Castellví-Bel, Sergi, Chan, Andrew T., Cheng, Iona, Gruber, Stephen, van Guelpen, Bethany, Li, Christopher I., Le Marchand, Loic, Newcomb, Polly A., Ogino, Shuji, Pellatt, Andrew, Schmit, Stephanie L., Wolk, Alicja, Wu, Anna H., Peters, Ulrike, Gunter, Marc J., Tsilidis, Konstantinos K., Bouras, Emmanouil, Gill, Dipender, Zuber, Verena, Murphy, Neil, Dimou, Niki, Aleksandrova, Krasimira, Lewis, Sarah J., Martin, Richard M., Yarmolinsky, James, Albanes, Demetrius, Brenner, Hermann, Castellví-Bel, Sergi, Chan, Andrew T., Cheng, Iona, Gruber, Stephen, van Guelpen, Bethany, Li, Christopher I., Le Marchand, Loic, Newcomb, Polly A., Ogino, Shuji, Pellatt, Andrew, Schmit, Stephanie L., Wolk, Alicja, Wu, Anna H., Peters, Ulrike, Gunter, Marc J., and Tsilidis, Konstantinos K.
- Abstract
Background: Colorectal cancer (CRC) is the third-most-common cancer worldwide and its rates are increasing. Elevated body mass index (BMI) is an established risk factor for CRC, although the molecular mechanisms behind this association remain unclear. Using the Mendelian randomization (MR) framework, we aimed to investigate the mediating effects of putative biomarkers and other CRC risk factors in the association between BMI and CRC. Methods: We selected as mediators biomarkers of established cancer-related mechanisms and other CRC risk factors for which a plausible association with obesity exists, such as inflammatory biomarkers, glucose homeostasis traits, lipids, adipokines, insulin-like growth factor 1 (IGF1), sex hormones, 25-hydroxy-vitamin D, smoking, physical activity (PA) and alcohol consumption. We used inverse-variance weighted MR in the main univariable analyses and performed sensitivity analyses (weighted-median, MR–Egger, Contamination Mixture). We used multivariable MR for the mediation analyses. Results: Genetically predicted BMI was positively associated with CRC risk [odds ratio per SD (5 kg/m2) ¼ 1.17, 95% CI: 1.08–1.24, P-value ¼ 1.4 × 10−5] and robustly associated with nearly all potential mediators. Genetically predicted IGF1, fasting insulin, low-density lipoprotein cholesterol, smoking, PA and alcohol were associated with CRC risk. Evidence for attenuation was found for IGF1 [explained 7% (95% CI: 2–13%) of the association], smoking (31%, 4–57%) and PA (7%, 2–11%). There was little evidence for pleiotropy, although smoking was bidirectionally associated with BMI and instruments were weak for PA. Conclusions: The effect of BMI on CRC risk is possibly partly mediated through plasma IGF1, whereas the attenuation of the BMI–CRC association by smoking and PA may reflect confounding and shared underlying mechanisms rather than mediation.
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- 2024
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36. Post-diagnosis adiposity and colorectal cancer prognosis:A Global Cancer Update Programme (CUP Global) systematic literature review and meta-analysis
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Becerra-Tomás, Nerea, Markozannes, Georgios, Cariolou, Margarita, Balducci, Katia, Vieira, Rita, Kiss, Sonia, Aune, Dagfinn, Greenwood, Darren C., Dossus, Laure, Copson, Ellen, Renehan, Andrew G., Bours, Martijn, Demark-Wahnefried, Wendy, Hudson, Melissa M., May, Anne M., Odedina, Folakemi T., Skinner, Roderick, Steindorf, Karen, Tjønneland, Anne, Velikova, Galina, Baskin, Monica L., Chowdhury, Rajiv, Hill, Lynette, Lewis, Sarah J., Seidell, Jaap, Weijenberg, Matty P., Krebs, John, Cross, Amanda J., Tsilidis, Konstantinos K., Chan, Doris S.M., Becerra-Tomás, Nerea, Markozannes, Georgios, Cariolou, Margarita, Balducci, Katia, Vieira, Rita, Kiss, Sonia, Aune, Dagfinn, Greenwood, Darren C., Dossus, Laure, Copson, Ellen, Renehan, Andrew G., Bours, Martijn, Demark-Wahnefried, Wendy, Hudson, Melissa M., May, Anne M., Odedina, Folakemi T., Skinner, Roderick, Steindorf, Karen, Tjønneland, Anne, Velikova, Galina, Baskin, Monica L., Chowdhury, Rajiv, Hill, Lynette, Lewis, Sarah J., Seidell, Jaap, Weijenberg, Matty P., Krebs, John, Cross, Amanda J., Tsilidis, Konstantinos K., and Chan, Doris S.M.
- Abstract
The adiposity influence on colorectal cancer prognosis remains poorly characterised. We performed a systematic review and meta-analysis on post-diagnosis adiposity measures (body mass index [BMI], waist circumference, waist-to-hip ratio, weight) or their changes and colorectal cancer outcomes. PubMed and Embase were searched through 28 February 2022. Random-effects meta-analyses were conducted when at least three studies had sufficient information. The quality of evidence was interpreted and graded by the Global Cancer Update Programme (CUP Global) independent Expert Committee on Cancer Survivorship and Expert Panel. We reviewed 124 observational studies (85 publications). Meta-analyses were possible for BMI and all-cause mortality, colorectal cancer-specific mortality, and cancer recurrence/disease-free survival. Non-linear meta-analysis indicated a reverse J-shaped association between BMI and colorectal cancer outcomes (nadir at BMI 28 kg/m2). The highest risk, relative to the nadir, was observed at both ends of the BMI distribution (18 and 38 kg/m2), namely 60% and 23% higher risk for all-cause mortality; 95% and 26% for colorectal cancer-specific mortality; and 37% and 24% for cancer recurrence/disease-free survival, respectively. The higher risk with low BMI was attenuated in secondary analyses of RCTs (compared to cohort studies), among studies with longer follow-up, and in women suggesting potential methodological limitations and/or altered physiological state. Descriptively synthesised studies on other adiposity-outcome associations of interest were limited in number and methodological quality. All the associations were graded as limited (likelihood of causality: no conclusion) due to potential methodological limitations (reverse causation, confounding, selection bias). Additional well-designed observational studies and interventional trials are needed to provide further clarification., The adiposity influence on colorectal cancer prognosis remains poorly characterised. We performed a systematic review and meta-analysis on post-diagnosis adiposity measures (body mass index [BMI], waist circumference, waist-to-hip ratio, weight) or their changes and colorectal cancer outcomes. PubMed and Embase were searched through 28 February 2022. Random-effects meta-analyses were conducted when at least three studies had sufficient information. The quality of evidence was interpreted and graded by the Global Cancer Update Programme (CUP Global) independent Expert Committee on Cancer Survivorship and Expert Panel. We reviewed 124 observational studies (85 publications). Meta-analyses were possible for BMI and all-cause mortality, colorectal cancer-specific mortality, and cancer recurrence/disease-free survival. Non-linear meta-analysis indicated a reverse J-shaped association between BMI and colorectal cancer outcomes (nadir at BMI 28 kg/m2). The highest risk, relative to the nadir, was observed at both ends of the BMI distribution (18 and 38 kg/m2), namely 60% and 23% higher risk for all-cause mortality; 95% and 26% for colorectal cancer-specific mortality; and 37% and 24% for cancer recurrence/disease-free survival, respectively. The higher risk with low BMI was attenuated in secondary analyses of RCTs (compared to cohort studies), among studies with longer follow-up, and in women suggesting potential methodological limitations and/or altered physiological state. Descriptively synthesised studies on other adiposity-outcome associations of interest were limited in number and methodological quality. All the associations were graded as limited (likelihood of causality: no conclusion) due to potential methodological limitations (reverse causation, confounding, selection bias). Additional well-designed observational studies and interventional trials are needed to provide further clarification.
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- 2024
37. Post-diagnosis dietary factors, supplement use and colorectal cancer prognosis:A Global Cancer Update Programme (CUP Global) systematic literature review and meta-analysis
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Chan, Doris S.M., Cariolou, Margarita, Markozannes, Georgios, Balducci, Katia, Vieira, Rita, Kiss, Sonia, Becerra-Tomás, Nerea, Aune, Dagfinn, Greenwood, Darren C., González-Gil, Esther M., Copson, Ellen, Renehan, Andrew G., Bours, Martijn, Demark-Wahnefried, Wendy, Hudson, Melissa M., May, Anne M., Odedina, Folakemi T., Skinner, Roderick, Steindorf, Karen, Tjønneland, Anne, Velikova, Galina, Baskin, Monica L., Chowdhury, Rajiv, Hill, Lynette, Lewis, Sarah J., Seidell, Jaap, Weijenberg, Matty P., Krebs, John, Cross, Amanda J., Tsilidis, Konstantinos K., Chan, Doris S.M., Cariolou, Margarita, Markozannes, Georgios, Balducci, Katia, Vieira, Rita, Kiss, Sonia, Becerra-Tomás, Nerea, Aune, Dagfinn, Greenwood, Darren C., González-Gil, Esther M., Copson, Ellen, Renehan, Andrew G., Bours, Martijn, Demark-Wahnefried, Wendy, Hudson, Melissa M., May, Anne M., Odedina, Folakemi T., Skinner, Roderick, Steindorf, Karen, Tjønneland, Anne, Velikova, Galina, Baskin, Monica L., Chowdhury, Rajiv, Hill, Lynette, Lewis, Sarah J., Seidell, Jaap, Weijenberg, Matty P., Krebs, John, Cross, Amanda J., and Tsilidis, Konstantinos K.
- Abstract
The role of diet in colorectal cancer prognosis is not well understood and specific lifestyle recommendations are lacking. We searched for randomised controlled trials (RCTs) and longitudinal observational studies on post-diagnosis dietary factors, supplement use and colorectal cancer survival outcomes in PubMed and Embase from inception until 28th February 2022. Random-effects dose–response meta-analyses were conducted when at least three studies had sufficient information. The evidence was interpreted and graded by the CUP Global independent Expert Committee on Cancer Survivorship and Expert Panel. Five RCTs and 35 observational studies were included (30,242 cases, over 8700 all-cause and 2100 colorectal cancer deaths, 3700 progression, recurrence, or disease-free events). Meta-analyses, including 3–10 observational studies each, were conducted for: whole grains, nuts/peanuts, red and processed meat, dairy products, sugary drinks, artificially sweetened beverages, coffee, alcohol, dietary glycaemic load/index, insulin load/index, marine omega-3 polyunsaturated fatty acids, supplemental calcium, circulating 25-hydroxyvitamin D (25[OH]D) and all-cause mortality; for alcohol, supplemental calcium, circulating 25(OH)D and colorectal cancer-specific mortality; and for circulating 25(OH)D and recurrence/disease-free survival. The overall evidence was graded as ‘limited’. The inverse associations between healthy dietary and/or lifestyle patterns (including diets that comprised plant-based foods), whole grains, total, caffeinated, or decaffeinated coffee and all-cause mortality and the positive associations between unhealthy dietary patterns, sugary drinks and all-cause mortality provided ‘limited—suggestive’ evidence. All other exposure-outcome associations provided ‘limited—no conclusion’ evidence. Additional, well-conducted cohort studies and carefully designed RCTs are needed to develop specific lifestyle recommendations for colorectal cancer survivors., The role of diet in colorectal cancer prognosis is not well understood and specific lifestyle recommendations are lacking. We searched for randomised controlled trials (RCTs) and longitudinal observational studies on post-diagnosis dietary factors, supplement use and colorectal cancer survival outcomes in PubMed and Embase from inception until 28th February 2022. Random-effects dose–response meta-analyses were conducted when at least three studies had sufficient information. The evidence was interpreted and graded by the CUP Global independent Expert Committee on Cancer Survivorship and Expert Panel. Five RCTs and 35 observational studies were included (30,242 cases, over 8700 all-cause and 2100 colorectal cancer deaths, 3700 progression, recurrence, or disease-free events). Meta-analyses, including 3–10 observational studies each, were conducted for: whole grains, nuts/peanuts, red and processed meat, dairy products, sugary drinks, artificially sweetened beverages, coffee, alcohol, dietary glycaemic load/index, insulin load/index, marine omega-3 polyunsaturated fatty acids, supplemental calcium, circulating 25-hydroxyvitamin D (25[OH]D) and all-cause mortality; for alcohol, supplemental calcium, circulating 25(OH)D and colorectal cancer-specific mortality; and for circulating 25(OH)D and recurrence/disease-free survival. The overall evidence was graded as ‘limited’. The inverse associations between healthy dietary and/or lifestyle patterns (including diets that comprised plant-based foods), whole grains, total, caffeinated, or decaffeinated coffee and all-cause mortality and the positive associations between unhealthy dietary patterns, sugary drinks and all-cause mortality provided ‘limited—suggestive’ evidence. All other exposure-outcome associations provided ‘limited—no conclusion’ evidence. Additional, well-conducted cohort studies and carefully designed RCTs are needed to develop specific lifestyle recommendations for colorectal cancer survivors.
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- 2024
38. Post-diagnosis physical activity and sedentary behaviour and colorectal cancer prognosis:A Global Cancer Update Programme (CUP Global) systematic literature review and meta-analysis
- Author
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Markozannes, Georgios, Becerra-Tomás, Nerea, Cariolou, Margarita, Balducci, Katia, Vieira, Rita, Kiss, Sonia, Aune, Dagfinn, Greenwood, Darren C., Gunter, Marc J., Copson, Ellen, Renehan, Andrew G., Bours, Martijn, Demark-Wahnefried, Wendy, Hudson, Melissa M., May, Anne M., Odedina, Folakemi T., Skinner, Roderick, Steindorf, Karen, Tjønneland, Anne, Velikova, Galina, Baskin, Monica L., Chowdhury, Rajiv, Hill, Lynette, Lewis, Sarah J., Seidell, Jaap, Weijenberg, Matty P., Krebs, John, Cross, Amanda J., Tsilidis, Konstantinos K., Chan, Doris S.M., Markozannes, Georgios, Becerra-Tomás, Nerea, Cariolou, Margarita, Balducci, Katia, Vieira, Rita, Kiss, Sonia, Aune, Dagfinn, Greenwood, Darren C., Gunter, Marc J., Copson, Ellen, Renehan, Andrew G., Bours, Martijn, Demark-Wahnefried, Wendy, Hudson, Melissa M., May, Anne M., Odedina, Folakemi T., Skinner, Roderick, Steindorf, Karen, Tjønneland, Anne, Velikova, Galina, Baskin, Monica L., Chowdhury, Rajiv, Hill, Lynette, Lewis, Sarah J., Seidell, Jaap, Weijenberg, Matty P., Krebs, John, Cross, Amanda J., Tsilidis, Konstantinos K., and Chan, Doris S.M.
- Abstract
Low physical activity and high sedentary behaviour have been clearly linked with colorectal cancer development, yet data on their potential role in colorectal cancer survival is limited. Better characterisation of these relationships is needed for the development of post-diagnosis physical activity and sedentary behaviour guidance for colorectal cancer survivors. We searched PubMed and Embase through 28 February 2022 for studies assessing post-diagnosis physical activity, and/or sedentary behaviour in relation to all-cause and cause-specific mortality and recurrence after colorectal cancer diagnosis. Total and recreational physical activity were assessed overall and by frequency, duration, intensity, and volume using categorical, linear, and non-linear dose–response random-effects meta-analyses. The Global Cancer Update Programme (CUP Global) independent Expert Committee on Cancer Survivorship and Expert Panel interpreted and graded the likelihood of causality. We identified 16 observational studies on 82,220 non-overlapping patients from six countries. Physical activity was consistently inversely associated with colorectal cancer morbidity and mortality outcomes, with 13%–60% estimated reductions in risk. Sedentary behaviour was positively associated with all-cause mortality. The evidence had methodological limitations including potential confounding, selection bias and reverse causation, coupled with a limited number of studies for most associations. The CUP Global Expert panel concluded limited-suggestive evidence for recreational physical activity with all-cause mortality and cancer recurrence. Total physical activity and its specific domains and dimensions, and sedentary behaviour were all graded as limited-no conclusion for all outcomes. Future research should focus on randomised trials, while observational studies should obtain objective and repeated physical activity measures and better adjustment for confounders., Low physical activity and high sedentary behaviour have been clearly linked with colorectal cancer development, yet data on their potential role in colorectal cancer survival is limited. Better characterisation of these relationships is needed for the development of post-diagnosis physical activity and sedentary behaviour guidance for colorectal cancer survivors. We searched PubMed and Embase through 28 February 2022 for studies assessing post-diagnosis physical activity, and/or sedentary behaviour in relation to all-cause and cause-specific mortality and recurrence after colorectal cancer diagnosis. Total and recreational physical activity were assessed overall and by frequency, duration, intensity, and volume using categorical, linear, and non-linear dose–response random-effects meta-analyses. The Global Cancer Update Programme (CUP Global) independent Expert Committee on Cancer Survivorship and Expert Panel interpreted and graded the likelihood of causality. We identified 16 observational studies on 82,220 non-overlapping patients from six countries. Physical activity was consistently inversely associated with colorectal cancer morbidity and mortality outcomes, with 13%–60% estimated reductions in risk. Sedentary behaviour was positively associated with all-cause mortality. The evidence had methodological limitations including potential confounding, selection bias and reverse causation, coupled with a limited number of studies for most associations. The CUP Global Expert panel concluded limited-suggestive evidence for recreational physical activity with all-cause mortality and cancer recurrence. Total physical activity and its specific domains and dimensions, and sedentary behaviour were all graded as limited-no conclusion for all outcomes. Future research should focus on randomised trials, while observational studies should obtain objective and repeated physical activity measures and better adjustment for confounders.
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- 2024
39. Post-diagnosis adiposity, physical activity, sedentary behaviour, dietary factors, supplement use and colorectal cancer prognosis:Global Cancer Update Programme (CUP Global) summary of evidence grading
- Author
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Tsilidis, Konstantinos K., Markozannes, Georgios, Becerra-Tomás, Nerea, Cariolou, Margarita, Balducci, Katia, Vieira, Rita, Kiss, Sonia, Aune, Dagfinn, Greenwood, Darren C., Dossus, Laure, González-Gil, Esther M., Gunter, Marc J., Allen, Kate, Brockton, Nigel T., Croker, Helen, Gordon-Dseagu, Vanessa L., Mitrou, Panagiota, Musuwo, Nicole, Wiseman, Martin J., Copson, Ellen, Renehan, Andrew G., Bours, Martijn, Demark-Wahnefried, Wendy, Hudson, Melissa M., May, Anne M., Odedina, Folakemi T., Skinner, Roderick, Steindorf, Karen, Tjønneland, Anne, Velikova, Galina, Baskin, Monica L., Chowdhury, Rajiv, Hill, Lynette, Lewis, Sarah J., Seidell, Jaap, Weijenberg, Matty P., Krebs, John, Cross, Amanda J., Chan, Doris S.M., Tsilidis, Konstantinos K., Markozannes, Georgios, Becerra-Tomás, Nerea, Cariolou, Margarita, Balducci, Katia, Vieira, Rita, Kiss, Sonia, Aune, Dagfinn, Greenwood, Darren C., Dossus, Laure, González-Gil, Esther M., Gunter, Marc J., Allen, Kate, Brockton, Nigel T., Croker, Helen, Gordon-Dseagu, Vanessa L., Mitrou, Panagiota, Musuwo, Nicole, Wiseman, Martin J., Copson, Ellen, Renehan, Andrew G., Bours, Martijn, Demark-Wahnefried, Wendy, Hudson, Melissa M., May, Anne M., Odedina, Folakemi T., Skinner, Roderick, Steindorf, Karen, Tjønneland, Anne, Velikova, Galina, Baskin, Monica L., Chowdhury, Rajiv, Hill, Lynette, Lewis, Sarah J., Seidell, Jaap, Weijenberg, Matty P., Krebs, John, Cross, Amanda J., and Chan, Doris S.M.
- Abstract
Based on the World Cancer Research Fund Global Cancer Update Programme, we performed systematic reviews and meta-analyses to investigate the association of post-diagnosis adiposity, physical activity, sedentary behaviour, and dietary factors with colorectal cancer prognosis. We searched PubMed and Embase until 28th February, 2022. An independent expert committee and expert panel graded the quality of evidence. A total of 167 unique publications were reviewed, and all but five were observational studies. The quality of the evidence was graded conservatively due to the high risk of several biases. There was evidence of non-linearity in the associations between body mass index and colorectal cancer prognosis. The associations appeared reverse J-shaped, and the quality of this evidence was graded as limited (likelihood of causality: limited-no conclusion). The evidence on recreational physical activity and lower risk of all-cause mortality (relative risk [RR] highest vs. lowest: 0.69, 95% confidence interval [CI]: 0.62–0.77) and recurrence/disease-free survival (RR: 0.80, 95% CI: 0.70–0.92) was graded as limited-suggestive. There was limited-suggestive evidence for the associations between healthy dietary and/or lifestyle patterns (including diets that comprised plant-based foods), intake of whole grains and coffee with lower risk of all-cause mortality, and between unhealthy dietary patterns and intake of sugary drinks with higher risk of all-cause mortality. The evidence for other exposures on colorectal cancer outcomes was sparse and graded as limited-no conclusion. Analyses were conducted excluding cancer patients with metastases without substantial changes in the findings. Well-designed intervention and cohort studies are needed to support the development of lifestyle recommendations for colorectal cancer patients., Based on the World Cancer Research Fund Global Cancer Update Programme, we performed systematic reviews and meta-analyses to investigate the association of post-diagnosis adiposity, physical activity, sedentary behaviour, and dietary factors with colorectal cancer prognosis. We searched PubMed and Embase until 28th February, 2022. An independent expert committee and expert panel graded the quality of evidence. A total of 167 unique publications were reviewed, and all but five were observational studies. The quality of the evidence was graded conservatively due to the high risk of several biases. There was evidence of non-linearity in the associations between body mass index and colorectal cancer prognosis. The associations appeared reverse J-shaped, and the quality of this evidence was graded as limited (likelihood of causality: limited-no conclusion). The evidence on recreational physical activity and lower risk of all-cause mortality (relative risk [RR] highest vs. lowest: 0.69, 95% confidence interval [CI]: 0.62–0.77) and recurrence/disease-free survival (RR: 0.80, 95% CI: 0.70–0.92) was graded as limited-suggestive. There was limited-suggestive evidence for the associations between healthy dietary and/or lifestyle patterns (including diets that comprised plant-based foods), intake of whole grains and coffee with lower risk of all-cause mortality, and between unhealthy dietary patterns and intake of sugary drinks with higher risk of all-cause mortality. The evidence for other exposures on colorectal cancer outcomes was sparse and graded as limited-no conclusion. Analyses were conducted excluding cancer patients with metastases without substantial changes in the findings. Well-designed intervention and cohort studies are needed to support the development of lifestyle recommendations for colorectal cancer patients.
- Published
- 2024
40. Improving radiologist's ability in identifying particular abnormal lesions on mammograms through training test set with immediate feedback
- Author
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Trieu, Phuong Dung (Yun), Lewis, Sarah J., Li, Tong, Ho, Karen, Wong, Dennis J., Tran, Oanh T. M., Puslednik, Louise, Black, Deborah, and Brennan, Patrick C.
- Published
- 2021
- Full Text
- View/download PDF
41. Global processing provides malignancy evidence complementary to the information captured by humans or machines following detailed mammogram inspection
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Gandomkar, Ziba, Siviengphanom, Somphone, Ekpo, Ernest U., Suleiman, Mo’ayyad, Taba, Seyedamir Tavakoli, Li, Tong, Xu, Dong, Evans, Karla K., Lewis, Sarah J., Wolfe, Jeremy M., and Brennan, Patrick C.
- Published
- 2021
- Full Text
- View/download PDF
42. Familiarity, confidence and preference of artificial intelligence feedback and prompts by Australian breast cancer screening readers.
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Trieu, Phuong Dung, Barron, Melissa L., Jiang, Zhengqiang, Tavakoli Taba, Seyedamir, Gandomkar, Ziba, and Lewis, Sarah J.
- Subjects
BREAST tumor diagnosis ,SCALE analysis (Psychology) ,RESEARCH funding ,DATA analysis ,EARLY detection of cancer ,ARTIFICIAL intelligence ,QUESTIONNAIRES ,CONFIDENCE ,DESCRIPTIVE statistics ,CHI-squared test ,SURVEYS ,MAMMOGRAMS ,ATTITUDES of medical personnel ,CLINICAL competence ,STATISTICS ,RADIOLOGISTS ,DATA analysis software ,COMPARATIVE studies ,PSYCHOSOCIAL factors - Abstract
Objectives: This study explored the familiarity, perceptions and confidence of Australian radiology clinicians involved in reading screening mammograms, regarding artificial intelligence (AI) applications in breast cancer detection. Methods: Sixty-five radiologists, breast physicians and radiology trainees participated in an online survey that consisted of 23 multiple choice questions asking about their experience and familiarity with AI products. Furthermore, the survey asked about their confidence in using AI outputs and their preference for AI modes applied in a breast screening context. Participants' responses to questions were compared using Pearson's χ
2 test. Bonferroni-adjusted significance tests were used for pairwise comparisons. Results: Fifty-five percent of respondents had experience with AI in their workplaces, with automatic density measurement powered by machine learning being the most familiar AI product (69.4%). The top AI outputs with the highest ranks of perceived confidence were 'Displaying suspicious areas on mammograms with the percentage of cancer possibility' (67.8%) and 'Automatic mammogram classification (normal, benign, cancer, uncertain)' (64.6%). Radiology and breast physicians preferred using AI as second-reader mode (75.4% saying 'somewhat happy' to 'extremely happy') over triage (47.7%), pre-screening and first-reader modes (both with 26.2%) (P < 0.001). Conclusion: The majority of screen readers expressed increased confidence in utilising AI for highlighting suspicious areas on mammograms and for automatically classifying mammograms. They considered AI as an optimal second-reader mode being the most ideal use in a screening program. The findings provide valuable insights into the familiarities and expectations of radiologists and breast clinicians for the AI products that can enhance the effectiveness of the breast cancer screening programs, benefitting both healthcare professionals and patients alike. What is known about the topic? Artificial intelligence (AI) holds promise in providing computer-aided detection in health care, however, current research suggests that standalone AI applications in clinical practice fall short of matching the accuracy of a single radiologist. What does this paper add? The study showed a significant preference among clinicians for using AI as a supplementary tool, serving as a second-reader. Such an integrated approach, where AI aids in flagging suspicious areas on mammograms or offers automatic classification, reflects the ideal cooperation between breast screening readers and AI systems. What are the implications for practitioners? These insights shed light on clinicians' familiarity with and expectations of AI tools that can boost the effectiveness of breast screening programs. [ABSTRACT FROM AUTHOR]- Published
- 2024
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- View/download PDF
43. Evaluating Recalibrating AI Models for Breast Cancer Diagnosis in a New Context: Insights from Transfer Learning, Image Enhancement and High Quality Training Data Integration
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Jiang, Zhengqiang, primary, Gandomkar, Ziba, additional, Trieu, Phuong Dung, additional, Taba, Seyedamir Tavakoli, additional, Barron, Melissa L., additional, Obeidy, Peyman, additional, and Lewis, Sarah J., additional
- Published
- 2023
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- View/download PDF
44. Computer-extracted global radiomic features can predict the radiologists’ first impression about the abnormality of a screening mammogram
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Siviengphanom, Somphone, primary, Lewis, Sarah J, additional, Brennan, Patrick C, additional, and Gandomkar, Ziba, additional
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- 2023
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- View/download PDF
45. Environmental and genetic predictors of whole blood mercury and selenium concentrations in pregnant women in a UK birth cohort.
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Dack, Kyle, primary, Huang, Peiyuan, additional, Taylor, Caroline M, additional, Rai, Dheeraj, additional, and Lewis, Sarah J, additional
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- 2023
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46. Genome-Wide Association Study of Blood Mercury in European Pregnant Women and Children
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Dack, Kyle, primary, Bustamante, Mariona, additional, Taylor, Caroline M., additional, Llop, Sabrina, additional, Lozano, Manuel, additional, Yousefi, Paul, additional, Gražulevičienė, Regina, additional, Gutzkow, Kristine Bjerve, additional, Brantsæter, Anne Lise, additional, Mason, Dan, additional, Escaramís, Georgia, additional, and Lewis, Sarah J., additional
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- 2023
- Full Text
- View/download PDF
47. Mendelian randomization does not support serum calcium in prostate cancer risk
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Yarmolinsky, James, Berryman, Katie, Langdon, Ryan, Bonilla, Carolina, Smith, George Davey, Martin, Richard M., and Lewis, Sarah J.
- Published
- 2018
48. Radiation Therapy Patient Education Review and a Case Study Using the Virtual Environment for Radiotherapy Training System
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Jimenez, Yobelli A. and Lewis, Sarah J.
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- 2018
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49. The Albatross Plot: A Novel Graphical Tool for Presenting Results of Diversely Reported Studies in a Systematic Review
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Harrison, Sean, Jones, Hayley E., Martin, Richard M., Lewis, Sarah J., and Higgins, Julian P. T.
- Abstract
Meta-analyses combine the results of multiple studies of a common question. Approaches based on effect size estimates from each study are generally regarded as the most informative. However, these methods can only be used if comparable effect sizes can be computed from each study, and this may not be the case due to variation in how the studies were done or limitations in how their results were reported. Other methods, such as vote counting, are then used to summarize the results of these studies, but most of these methods are limited in that they do not provide any indication of the magnitude of effect. We propose a novel plot, the albatross plot, which requires only a 1-sided P value and a total sample size from each study (or equivalently a 2-sided P value, direction of effect and total sample size). The plot allows an approximate examination of underlying effect sizes and the potential to identify sources of heterogeneity across studies. This is achieved by drawing contours showing the range of effect sizes that might lead to each P value for given sample sizes, under simple study designs. We provide examples of albatross plots using data from previous meta-analyses, allowing for comparison of results, and an example from when a meta-analysis was not possible.
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- 2017
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50. Does milk intake promote prostate cancer initiation or progression via effects on insulin-like growth factors (IGFs)? A systematic review and meta-analysis
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Harrison, Sean, Lennon, Rosie, Holly, Jeff, Higgins, Julian P. T., Gardner, Mike, Perks, Claire, Gaunt, Tom, Tan, Vanessa, Borwick, Cath, Emmet, Pauline, Jeffreys, Mona, Northstone, Kate, Rinaldi, Sabina, Thomas, Stephen, Turner, Suzanne D., Pease, Anna, Vilenchick, Vicky, Martin, Richard M., and Lewis, Sarah J.
- Published
- 2017
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