12 results on '"Kalsbeek, Anya"'
Search Results
2. Omega-6 fatty acid biomarkers and incident type 2 diabetes: pooled analysis of individual-level data for 39 740 adults from 20 prospective cohort studies
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Wu, Jason H Y, Marklund, Matti, Imamura, Fumiaki, Tintle, Nathan, Ardisson Korat, Andres V, de Goede, Janette, Zhou, Xia, Yang, Wei-Sin, de Oliveira Otto, Marcia C, Kröger, Janine, Qureshi, Waqas, Virtanen, Jyrki K, Bassett, Julie K, Frazier-Wood, Alexis C, Lankinen, Maria, Murphy, Rachel A, Rajaobelina, Kalina, Del Gobbo, Liana C, Forouhi, Nita G, Luben, Robert, Khaw, Kay-Tee, Wareham, Nick, Kalsbeek, Anya, Veenstra, Jenna, Luo, Juhua, Hu, Frank B, Lin, Hung-Ju, Siscovick, David S, Boeing, Heiner, Chen, Tzu-An, Steffen, Brian, Steffen, Lyn M, Hodge, Allison, Eriksdottir, Gudny, Smith, Albert V, Gudnason, Vilmunder, Harris, Tamara B, Brouwer, Ingeborg A, Berr, Claudine, Helmer, Catherine, Samieri, Cecilia, Laakso, Markku, Tsai, Michael Y, Giles, Graham G, Nurmi, Tarja, Wagenknecht, Lynne, Schulze, Matthias B, Lemaitre, Rozenn N, Chien, Kuo-Liong, Soedamah-Muthu, Sabita S, Geleijnse, Johanna M, Sun, Qi, Harris, William S, Lind, Lars, Ärnlöv, Johan, Riserus, Ulf, Micha, Renata, and Mozaffarian, Dariush
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- 2017
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3. Biomarkers of Dietary Omega-6 Fatty Acids and Incident Cardiovascular Disease and Mortality: An Individual-Level Pooled Analysis of 30 Cohort Studies
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Marklund, Matti, Wu, Jason H.Y., Imamura, Fumiaki, Del Gobbo, Liana C., Fretts, Amanda, de Goede, Janette, Shi, Peilin, Tintle, Nathan, Wennberg, Maria, Aslibekyan, Stella, Chen, Tzu-An, de Oliveira Otto, Marcia C., Hirakawa, Yoichiro, Eriksen, Helle Højmark, Kröger, Janine, Laguzzi, Federica, Lankinen, Maria, Murphy, Rachel A., Prem, Kiesha, Samieri, Cécilia, Virtanen, Jyrki, Wood, Alexis C., Wong, Kerry, Yang, Wei-Sin, Zhou, Xia, Baylin, Ana, Boer, Jolanda M.A., Brouwer, Ingeborg A., Campos, Hannia, Chaves, Paulo H. M., Chien, Kuo-Liong, de Faire, Ulf, Djoussé, Luc, Eiriksdottir, Gudny, El-Abbadi, Naglaa, Forouhi, Nita G., Gaziano, J. Michael, Geleijnse, Johanna M., Gigante, Bruna, Giles, Graham, Guallar, Eliseo, Gudnason, Vilmundur, Harris, Tamara, Harris, William S., Helmer, Catherine, Hellenius, Mai-Lis, Hodge, Allison, Hu, Frank B., Jacques, Paul F., Jansson, Jan-Håkan, Kalsbeek, Anya, Khaw, Kay-Tee, Koh, Woon-Puay, Laakso, Markku, Leander, Karin, Lin, Hung-Ju, Lind, Lars, Luben, Robert, Luo, Juhua, McKnight, Barbara, Mursu, Jaakko, Ninomiya, Toshiharu, Overvad, Kim, Psaty, Bruce M., Rimm, Eric, Schulze, Matthias B., Siscovick, David, Skjelbo Nielsen, Michael, Smith, Albert V., Steffen, Brian T., Steffen, Lyn, Sun, Qi, Sundström, Johan, Tsai, Michael Y., Tunstall-Pedoe, Hugh, Uusitupa, Matti I. J., van Dam, Rob M., Veenstra, Jenna, Verschuren, W.M. Monique, Wareham, Nick, Willett, Walter, Woodward, Mark, Yuan, Jian-Min, Micha, Renata, Lemaitre, Rozenn N, Mozaffarian, Dariush, and Risérus, Ulf
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- 2019
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4. Evaluating the performance of gene-based tests of genetic association when testing for association between methylation and change in triglyceride levels at GAW20
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Vander Woude, Jason, Huisman, Jordan, Vander Berg, Lucas, Veenstra, Jenna, Bos, Abbey, Kalsbeek, Anya, Koster, Karissa, Ryder, Nathan, and Tintle, Nathan L.
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- 2018
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5. Epigenome wide association study of SNP–CpG interactions on changes in triglyceride levels after pharmaceutical intervention: a GAW20 analysis
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Veenstra, Jenna, Kalsbeek, Anya, Koster, Karissa, Ryder, Nathan, Bos, Abbey, Huisman, Jordan, VanderBerg, Lucas, VanderWoude, Jason, and Tintle, Nathan L.
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- 2018
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6. Impact of cerebrovascular accidents on lung transplant survival
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Kalsbeek, Anya, primary, Chuckaree, Ishwar, additional, Khoury, Mitri K., additional, Leonard, Grey, additional, Maaraoui, Kayla, additional, Liu, Charles, additional, Hackmann, Amy, additional, Huffman, Lynn C., additional, Peltz, Matthias, additional, Ring, W. Steves, additional, Wait, Michael A., additional, and Heid, Christopher A., additional
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- 2022
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7. Cardiac transplantation in adults with congenital heart disease: A single center case series
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Heid, Christopher A., primary, Chandra, Raghav, additional, Liu, Charles, additional, Pruszynski, Jessica, additional, Khoury, Mitri K., additional, Vela, Ryan, additional, Zeng, Xue, additional, Maaraoui, Kayla, additional, Kalsbeek, Anya, additional, Ring, W. Steves, additional, Amin, Alpesh, additional, Murala, John, additional, and Peltz, Matthias, additional
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- 2021
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8. Associations of circulating very-long-chain saturated fatty acids and incident type 2 diabetes : a pooled analysis of prospective cohort studies
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Fretts, Amanda M., Imamura, Fumiaki, Marklund, Matti, Micha, Renata, Wu, Jason H. Y., Murphy, Rachel A., Chien, Kuo-Liong, McKnight, Barbara, Tintle, Nathan, Forouhi, Nita G., Qureshi, Waqas T., Virtanen, Jyrki K., Wong, Kerry, Wood, Alexis C., Lankinen, Maria, Rajaobelina, Kalina, Harris, Tamara B., Djousse, Luc, Harris, Bill, Wareham, Nick J., Steffen, Lyn M., Laakso, Markku, Veenstra, Jenna, Samieri, Cecilia, Brouwer, Ingeborg A., Yu, Chaoyu Ian, Koulman, Albert, Steffen, Brian T., Helmer, Catherine, Sotoodehnia, Nona, Siscovick, David, Gudnason, Vilmundur, Consortium, InterAct, Wagenknecht, Lynne, Voutilainen, Sari, Tsai, Michael Y., Uusitupa, Matti, Kalsbeek, Anya, Berr, Claudine, Mozaffarian, Dariush, Lemaitre, Rozenn N., Fretts, Amanda M., Imamura, Fumiaki, Marklund, Matti, Micha, Renata, Wu, Jason H. Y., Murphy, Rachel A., Chien, Kuo-Liong, McKnight, Barbara, Tintle, Nathan, Forouhi, Nita G., Qureshi, Waqas T., Virtanen, Jyrki K., Wong, Kerry, Wood, Alexis C., Lankinen, Maria, Rajaobelina, Kalina, Harris, Tamara B., Djousse, Luc, Harris, Bill, Wareham, Nick J., Steffen, Lyn M., Laakso, Markku, Veenstra, Jenna, Samieri, Cecilia, Brouwer, Ingeborg A., Yu, Chaoyu Ian, Koulman, Albert, Steffen, Brian T., Helmer, Catherine, Sotoodehnia, Nona, Siscovick, David, Gudnason, Vilmundur, Consortium, InterAct, Wagenknecht, Lynne, Voutilainen, Sari, Tsai, Michael Y., Uusitupa, Matti, Kalsbeek, Anya, Berr, Claudine, Mozaffarian, Dariush, and Lemaitre, Rozenn N.
- Abstract
Background: Saturated fatty acids (SFAs) of different chain lengths have unique metabolic and biological effects, and a small number of recent studies suggest that higher circulating concentrations of the very-long-chain SFAs (VLSFAs) arachidic acid (20:0), behenic acid (22:0), and lignoceric acid (24:0) are associated with a lower risk of diabetes. Confirmation of these findings in a large and diverse population is needed. Objective: We investigated the associations of circulating VLSFAs 20:0, 22:0, and 24:0 with incident type 2 diabetes in prospective studies. Methods: Twelve studies that are part of the Fatty Acids and Outcomes Research Consortium participated in the analysis. Using Cox or logistic regression within studies and an inverse-variance-weighted meta-analysis across studies, we examined the associations of VLSFAs 20:0, 22:0, and 24:0 with incident diabetes among 51,431 participants. Results: There were 14,276 cases of incident diabetes across participating studies. Higher circulating concentrations of 20:0, 22:0, and 24:0 were each associated with a lower risk of incident diabetes. Pooling across cohorts, the RR (95% CI) for incident diabetes comparing the 90th percentile to the 10th percentile was 0.78 (0.70, 0.87) for 20:0, 0.84 (0.77, 0.91) for 22:0, and 0.75 (0.69, 0.83) for 24:0 after adjustment for demographic, lifestyle, adiposity, and other health factors. Results were fully attenuated in exploratory models that adjusted for circulating 16:0 and triglycerides. Conclusions: Results from this pooled analysis indicate that higher concentrations of circulating VLSFAs 20:0, 22:0, and 24:0 are each associated with a lower risk of diabetes.
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- 2019
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9. A genome-wide association study of red-blood cell fatty acids and ratios incorporating dietary covariates: Framingham Heart Study Offspring Cohort
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Kalsbeek, Anya, primary, Veenstra, Jenna, additional, Westra, Jason, additional, Disselkoen, Craig, additional, Koch, Kristin, additional, McKenzie, Katelyn A., additional, O’Bott, Jacob, additional, Vander Woude, Jason, additional, Fischer, Karen, additional, Shearer, Greg C., additional, Harris, William S., additional, and Tintle, Nathan L., additional
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- 2018
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10. Genome-Wide Interaction Study of Omega-3 PUFAs and Other Fatty Acids on Inflammatory Biomarkers of Cardiovascular Health in the Framingham Heart Study
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Veenstra, Jenna, primary, Kalsbeek, Anya, additional, Westra, Jason, additional, Disselkoen, Craig, additional, E. Smith, Caren, additional, and Tintle, Nathan, additional
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- 2017
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11. Omega-6 fatty acid biomarkers and incident type 2 diabetes : pooled analysis of individual-level data for 39 740 adults from 20 prospective cohort studies
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Wu, Jason H. Y., Marklund, Matti, Imamura, Fumiaki, Tintle, Nathan, Korat, Andres V. Ardisson, de Goede, Janette, Zhou, Xia, Yang, Wei-Sin, Otto, Marcia C. de Oliveira, Kroger, Janine, Qureshi, Waqas, Virtanen, Jyrki K., Bassett, Julie K., Frazier-Wood, Alexis C., Lankinen, Maria, Murphy, Rachel A., Rajaobelina, Kalina, Del Gobbo, Liana C., Forouhi, Nita G., Luben, Robert, Khaw, Kay-Tee, Wareham, Nick, Kalsbeek, Anya, Veenstra, Jenna, Luo, Juhua, Hu, Frank B., Lin, Hung-Ju, Siscovick, David S., Boeing, Heiner, Chen, Tzu-An, Steffen, Brian, Steffen, Lyn M., Hodge, Allison, Eriksdottir, Gudny, Smith, Albert V., Gudnason, Vilmunder, Harris, Tamara B., Brouwer, Ingeborg A., Berr, Claudine, Helmer, Catherine, Samieri, Cecilia, Laakso, Markku, Tsai, Michael Y., Giles, Graham G., Nurmi, Tarja, Wagenknecht, Lynne, Schulze, Matthias B., Lemaitre, Rozenn N., Chien, Kuo-Liong, Soedamah-Muthu, Sabita S., Geleijnse, Johanna M., Sun, Qi, Harris, William S., Lind, Lars, Arnlov, Johan, Risérus, Ulf, Micha, Renata, Mozaffarian, Dariush, Wu, Jason H. Y., Marklund, Matti, Imamura, Fumiaki, Tintle, Nathan, Korat, Andres V. Ardisson, de Goede, Janette, Zhou, Xia, Yang, Wei-Sin, Otto, Marcia C. de Oliveira, Kroger, Janine, Qureshi, Waqas, Virtanen, Jyrki K., Bassett, Julie K., Frazier-Wood, Alexis C., Lankinen, Maria, Murphy, Rachel A., Rajaobelina, Kalina, Del Gobbo, Liana C., Forouhi, Nita G., Luben, Robert, Khaw, Kay-Tee, Wareham, Nick, Kalsbeek, Anya, Veenstra, Jenna, Luo, Juhua, Hu, Frank B., Lin, Hung-Ju, Siscovick, David S., Boeing, Heiner, Chen, Tzu-An, Steffen, Brian, Steffen, Lyn M., Hodge, Allison, Eriksdottir, Gudny, Smith, Albert V., Gudnason, Vilmunder, Harris, Tamara B., Brouwer, Ingeborg A., Berr, Claudine, Helmer, Catherine, Samieri, Cecilia, Laakso, Markku, Tsai, Michael Y., Giles, Graham G., Nurmi, Tarja, Wagenknecht, Lynne, Schulze, Matthias B., Lemaitre, Rozenn N., Chien, Kuo-Liong, Soedamah-Muthu, Sabita S., Geleijnse, Johanna M., Sun, Qi, Harris, William S., Lind, Lars, Arnlov, Johan, Risérus, Ulf, Micha, Renata, and Mozaffarian, Dariush
- Abstract
Background The metabolic effects of omega-6 polyunsaturated fatty acids (PUFAs) remain contentious, and little evidence is available regarding their potential role in primary prevention of type 2 diabetes. We aimed to assess the associations of linoleic acid and arachidonic acid biomarkers with incident type 2 diabetes. Methods We did a pooled analysis of new, harmonised, individual-level analyses for the biomarkers linoleic acid and its metabolite arachidonic acid and incident type 2 diabetes. We analysed data from 20 prospective cohort studies from ten countries (Iceland, the Netherlands, the USA, Taiwan, the UK, Germany, Finland, Australia, Sweden, and France), with biomarkers sampled between 1970 and 2010. Participants included in the analyses were aged 18 years or older and had data available for linoleic acid and arachidonic acid biomarkers at baseline. We excluded participants with type 2 diabetes at baseline. The main outcome was the association between omega-6 PUFA biomarkers and incident type 2 diabetes. We assessed the relative risk of type 2 diabetes prospectively for each cohort and lipid compartment separately using a prespecified analytic plan for exposures, covariates, effect modifiers, and analysis, and the findings were then pooled using inverse-variance weighted meta-analysis. Findings Participants were 39 740 adults, aged (range of cohort means) 49-76 years with a BMI (range of cohort means) of 23.3-28.4 kg/m(2), who did not have type 2 diabetes at baseline. During a follow-up of 366 073 person-years, we identified 4347 cases of incident type 2 diabetes. In multivariable-adjusted pooled analyses, higher proportions of linoleic acid biomarkers as percentages of total fatty acid were associated with a lower risk of type 2 diabetes overall (risk ratio [RR] per interquintile range 0.65, 95% CI 0.60-0.72, p<0.0001; I-2=53.9%, p(heterogeneity) = 0.002). The associations between linoleic acid biomarkers and type 2 diabetes were generally similar in d
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- 2017
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12. Biomarkers of Dietary Omega-6 Fatty Acids and Incident Cardiovascular Disease and Mortality
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Marklund, Matti, Wu, Jason HY, Imamura, Fumiaki, Del Gobbo, Liana C, Fretts, Amanda, De Goede, Janette, Shi, Peilin, Tintle, Nathan, Wennberg, Maria, Aslibekyan, Stella, Chen, Tzu-An, De Oliveira Otto, Marcia C, Hirakawa, Yoichiro, Eriksen, Helle Højmark, Kröger, Janine, Laguzzi, Federica, Lankinen, Maria, Murphy, Rachel A, Prem, Kiesha, Samieri, Cécilia, Virtanen, Jyrki, Wood, Alexis C, Wong, Kerry, Yang, Wei-Sin, Zhou, Xia, Baylin, Ana, Boer, Jolanda MA, Brouwer, Ingeborg A, Campos, Hannia, Chaves, Paulo HM, Chien, Kuo-Liong, De Faire, Ulf, Djoussé, Luc, Eiriksdottir, Gudny, El-Abbadi, Naglaa, Forouhi, Nita G, Michael Gaziano, J, Geleijnse, Johanna M, Gigante, Bruna, Giles, Graham, Guallar, Eliseo, Gudnason, Vilmundur, Harris, Tamara, Harris, William S, Helmer, Catherine, Hellenius, Mai-Lis, Hodge, Allison, Hu, Frank B, Jacques, Paul F, Jansson, Jan-Håkan, Kalsbeek, Anya, Khaw, Kay-Tee, Koh, Woon-Puay, Laakso, Markku, Leander, Karin, Lin, Hung-Ju, Lind, Lars, Luben, Robert, Luo, Juhua, McKnight, Barbara, Mursu, Jaakko, Ninomiya, Toshiharu, Overvad, Kim, Psaty, Bruce M, Rimm, Eric, Schulze, Matthias B, Siscovick, David, Skjelbo Nielsen, Michael, Smith, Albert V, Steffen, Brian T, Steffen, Lyn, Sun, Qi, Sundström, Johan, Tsai, Michael Y, Tunstall-Pedoe, Hugh, Uusitupa, Matti IJ, Van Dam, Rob M, Veenstra, Jenna, Monique Verschuren, WM, Wareham, Nick, Willett, Walter, Woodward, Mark, Yuan, Jian-Min, Micha, Renata, Lemaitre, Rozenn N, Mozaffarian, Dariush, Risérus, Ulf, and Cohorts For Heart And Aging Research In Genomic Epidemiology (CHARGE) Fatty Acids And Outcomes Research Consortium (FORCE)
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linoleic acid ,Male ,primary prevention ,biomarkers ,Middle Aged ,Protective Factors ,Recommended Dietary Allowances ,Dietary Fats ,Risk Assessment ,3. Good health ,cardiovascular diseases ,Observational Studies as Topic ,Risk Factors ,arachidonic acid ,Humans ,epidemiology ,Female ,Diet, Healthy ,diet ,Nutritive Value ,Risk Reduction Behavior ,Aged - Abstract
BACKGROUND: Global dietary recommendations for and cardiovascular effects of linoleic acid, the major dietary omega-6 fatty acid, and its major metabolite, arachidonic acid, remain controversial. To address this uncertainty and inform international recommendations, we evaluated how in vivo circulating and tissue levels of linoleic acid (LA) and arachidonic acid (AA) relate to incident cardiovascular disease (CVD) across multiple international studies. METHODS: We performed harmonized, de novo, individual-level analyses in a global consortium of 30 prospective observational studies from 13 countries. Multivariable-adjusted associations of circulating and adipose tissue LA and AA biomarkers with incident total CVD and subtypes (coronary heart disease, ischemic stroke, cardiovascular mortality) were investigated according to a prespecified analytic plan. Levels of LA and AA, measured as the percentage of total fatty acids, were evaluated linearly according to their interquintile range (ie, the range between the midpoint of the first and fifth quintiles), and categorically by quintiles. Study-specific results were pooled using inverse-variance-weighted meta-analysis. Heterogeneity was explored by age, sex, race, diabetes mellitus, statin use, aspirin use, omega-3 levels, and fatty acid desaturase 1 genotype (when available). RESULTS: In 30 prospective studies with medians of follow-up ranging 2.5 to 31.9 years, 15 198 incident cardiovascular events occurred among 68 659 participants. Higher levels of LA were significantly associated with lower risks of total CVD, cardiovascular mortality, and ischemic stroke, with hazard ratios per interquintile range of 0.93 (95% CI, 0.88-0.99), 0.78 (0.70-0.85), and 0.88 (0.79-0.98), respectively, and nonsignificantly with lower coronary heart disease risk (0.94; 0.88-1.00). Relationships were similar for LA evaluated across quintiles. AA levels were not associated with higher risk of cardiovascular outcomes; in a comparison of extreme quintiles, higher levels were associated with lower risk of total CVD (0.92; 0.86-0.99). No consistent heterogeneity by population subgroups was identified in the observed relationships. CONCLUSIONS: In pooled global analyses, higher in vivo circulating and tissue levels of LA and possibly AA were associated with lower risk of major cardiovascular events. These results support a favorable role for LA in CVD prevention.
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