16 results on '"Xie L"'
Search Results
2. Survival of women with breast cancer in Ottawa, Canada: variation with age, stage, histology, grade and treatment.
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Ugnat, A. M., Xie, L., Morris, J., Semenciw, R., and Mao, Y.
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BREAST cancer , *HISTOPATHOLOGY , *PROGNOSIS , *CANCER in women - Abstract
This study examined the 5-year survival of 2192 breast cancer women diagnosed between 1994 and 1997 in Ottawa, Canada, by age, TNM stage, histology, grade and treatment, including assessment of the independent value of variables in defining prognosis. Our results showed that age, stage, treatment and grade significantly influenced outcome regardless of the confounding factors considered, with histology failing to achieve significant independent prognostic information. The survival rates were highest at ages 50-69 years for stage I and at ages 40-49 years for stages II-IV. The rates were lowest at ages ?39 years for stages I-II and at ages ?70 years for stages III-IV. The differences in survival between grade 1 and grade 3 were 9% in stage I and 20% in stage II. The treatment leading to the best survival was surgery plus radiation for stages I-II and surgery combined with chemotherapy for stages III-IV. Lobular carcinoma had a better prognosis than ductal carcinoma; this can be explained by more grade 1 and less grade 3 cases in lobular carcinoma. The worse prognosis for young patients than other ages can be explained by their higher proportion of poorly differentiated cancers. Stage I patients aged 50-69 years having the best survival is likely due to the earlier diagnosis achieved through screening.British Journal of Cancer (2004) 90, 1138-1143. doi:10.1038/sj.bjc.6601662 www.bjcancer.com Published online 24 February 2004 [ABSTRACT FROM AUTHOR]
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- 2004
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3. Modeling heteroscedastic age-period-cohort cancer data.
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MacNeill, I. B., Mao, Y., and Xie, L.
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HETEROSCEDASTICITY ,CHANGE-point problems ,MATHEMATICAL statistics ,CANCER ,DEATH rate - Abstract
Copyright of Canadian Journal of Statistics is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 1994
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4. Incidence of childhood cancer in Canada during the COVID-19 pandemic.
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Pelland-Marcotte MC, Xie L, Barber R, Elkhalifa S, Frechette M, Kaur J, Onysko J, Bouffet E, Fernandez CV, Mitchell D, Rayar M, Randall A, Stammers D, Larouche V, Airhart A, Fidler-Benaoudia M, Cohen-Gogo S, Sung L, and Gibson P
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- Adolescent, Canada epidemiology, Child, Child, Preschool, Clinical Trials as Topic statistics & numerical data, Female, Humans, Incidence, Infant, Male, Neoplasms mortality, Retrospective Studies, SARS-CoV-2, Time Factors, COVID-19 epidemiology, Neoplasms epidemiology, Pandemics
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Background: The COVID-19 pandemic has had a major impact on access to health care resources. Our objective was to estimate the impact of the COVID-19 pandemic on the incidence of childhood cancer in Canada. We also aimed to compare the proportion of patients who enrolled in clinical trials at diagnosis, presented with metastatic disease or had an early death during the first 9 months of the COVID-19 pandemic compared with previous years., Methods: We conducted an observational study that included children younger than 15 years with a new diagnosis of cancer between March 2016 and November 2020 at 1 of 17 Canadian pediatric oncology centres. Our primary outcome was the monthly age-standardized incidence rates (ASIRs) of cancers. We evaluated level and trend changes using interventional autoregressive integrated moving average models. Secondary outcomes were the proportion of patients who were enrolled in a clinical trial, who had metastatic or advanced disease and who died within 30 days. We compared the baseline and pandemic periods using rate ratios (RRs) and 95% confidence intervals (CIs)., Results: Age-standardized incidence rates during COVID-19 quarters were 157.7, 164.6, and 148.0 per million, respectively, whereas quarterly baseline ASIRs ranged between 150.3 and 175.1 per million (incidence RR 0.93 [95% CI 0.78 to 1.12] to incidence RR 1.04 [95% CI 0.87 to 1.24]). We found no statistically significant level or slope changes between the projected and observed ASIRs for all new cancers (parameter estimate [β], level 4.98, 95% CI -15.1 to 25.04, p = 0.25), or when stratified by cancer type or by geographic area. Clinical trial enrolment rate was stable or increased during the pandemic compared with baseline (RR 1.22 [95% CI 0.70 to 2.13] to RR 1.71 [95% CI 1.01 to 2.89]). There was no difference in the proportion of patients with metastatic disease (RR 0.84 [95% CI 0.55 to 1.29] to RR 1.22 [0.84 to 1.79]), or who died within 30 days (RR 0.16 [95% CI 0.01 to 3.04] to RR 1.73 [95% CI 0.38 to 15.2])., Interpretation: We did not observe a statistically significant change in the incidence of childhood cancer, or in the proportion of children enrolling in a clinical trial, presenting with metastatic disease or who died early during the first 9 months of the COVID-19 pandemic, which suggests that access to health care in pediatric oncology was not reduced substantially in Canada., Competing Interests: Competing interests: None declared., (© 2021 CMA Joule Inc. or its licensors.)
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- 2021
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5. Causes and Characteristics of Children Unintentional Injuries in Emergency Department and Its Implications for Prevention.
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Gong H, Lu G, Ma J, Zheng J, Hu F, Liu J, Song J, Hu S, Sun L, Chen Y, Xie L, Zhang X, Duan L, and Xu H
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- Canada, Child, Child, Preschool, China epidemiology, Cross-Sectional Studies, Emergency Service, Hospital, Female, Humans, Male, Accidental Injuries
- Abstract
Background: Child unintentional injuries have become a hot topic worldwide, and substantial regional disparities existed in causes and characteristics. To date, limited data are available to investigate the causes and characteristics of child unintentional injuries from hospitals for children in China. Methods: A cross-sectional study was conducted between January 2017 and December 2018 in Shanghai, China. Patients aged <18 years with an unintentional injury presented to the emergency department were enrolled. Demographic information, Pediatric Risk for Mortality III score, and outcome variables were retrieved from electronic health records (EHRs). Frequencies and proportions of categorical variables and means and SDs of continuous variables are presented. Chi-square test and Student's t -test were used for the comparison between groups, as appropriate. Logistic regression analysis was used to estimate potential risk factors for admission to the hospital. Results: A total of 29,597 cases with unintentional injuries were identified between January 2017 and December 2018, with boys vs. girls ratio of 1.75. Preschool children account for approximately two-thirds of unintentional injuries in the emergency department. A distinctive pattern of mechanisms of unintentional injuries between gender was documented, and sports injury was significantly higher in boys than in girls (10.2 vs. 7.8%). Compared with Canadian Emergency Department Triage and Acuity Scale (CTAS) Grade 3 patients, Grade 2 [odds ratio (OR) = 2.99, 95% CI = 1.93-4.63, P < 0.001] and Grade 1 (OR = 74.85, 95% CI = 12.93-433.14, P < 0.001) patients had higher risk of inhospital admission. For causes of injuries, compared with falling, foreign body and poison had a lower risk of inhospital admission, while transport injury (OR = 1.31, 95% CI = 1.07-1.59, P = 0.008) and high fall injury (OR = 2.58. 95% CI =1.48-4.49, P < 0.001) had a significantly higher risk of admission. Conclusions: There was a significant relationship between age-groups and unintentional injuries between gender, with decreased injuries among girls growing up older. Preventive measures should be taken to reduce transport injury and high fall injury, which had a significantly higher risk of admission., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2021 Gong, Lu, Ma, Zheng, Hu, Liu, Song, Hu, Sun, Chen, Xie, Zhang, Duan and Xu.)
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- 2021
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6. Immunosuppression and Clostridioides (Clostridium) difficile Infection Risk in Metabolic and Bariatric Surgery Patients.
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Morales-Marroquin E, Xie L, Uppuluri M, Almandoz JP, Cruz-Muñoz N, and Messiah SE
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- Adult, Canada epidemiology, Clostridioides difficile immunology, Clostridium Infections immunology, Clostridium Infections microbiology, Female, Gastric Bypass statistics & numerical data, Gastroplasty statistics & numerical data, Humans, Laparoscopy adverse effects, Laparoscopy statistics & numerical data, Male, Middle Aged, Obesity, Morbid surgery, Postoperative Complications immunology, Postoperative Complications microbiology, Retrospective Studies, Risk Assessment statistics & numerical data, Risk Factors, United States epidemiology, Clostridium Infections epidemiology, Gastric Bypass adverse effects, Gastroplasty adverse effects, Immunosuppressive Agents adverse effects, Postoperative Complications epidemiology
- Abstract
Background: Immunosuppressant use increases risk of Clostridioides (Clostridium) difficile infection. To date, no studies have analyzed the relationship between immunosuppressant use and C difficile infections after metabolic and bariatric surgery (MBS)., Methods: A retrospective analysis of the 2015-2018 MBSAQIP data was conducted. The MBSAQIP data include information from 854 affiliated practices in the US and Canada. Initial sample size was 760,076 MBS patients. After excluding participants due to missing variables (n = 188,106) and the use of surgical procedures other than Roux-en-Y gastric bypass and sleeve gastroplasty (n = 129,712), final analyses were performed on 442,258 participants. Logistic regression models generated the odds of C difficile infection developing post MBS, according to immunosuppressant status (positive or negative)., Results: Unadjusted logistic regression analysis showed that patients using immunosuppressants were 95% more likely to have postoperative C difficile infection (odds ratio 1.945; 95% CI, 1.230 to 3.075; p < 0.001) vs MBS patients not taking immunosuppressants. After adjusting for age, sex, ethnicity, preoperative BMI, diabetes status, and surgical procedure type, the association remained unaffected (adjusted odds ratio 1.956; 95% CI, 1.236 to 3.095; p < 0.01). Patients who completed the laparoscopic Roux-en-Y gastric bypass procedure had more than double the odds of C difficile infection developing compared with those who completed the laparoscopic sleeve gastrectomy procedure (odds ratio 2.183; 95% CI, 1.842 to 2.587; p < 0.0001)., Conclusions: Our results using a population-based sample of MBS patients showed that those taking immunosuppressants have a significantly higher risk of developing Clostridioides (Clostridium) difficile infection postoperatively. These findings suggest that patients using immunosuppressants should be closely monitored both pre and post procedure., (Copyright © 2021 American College of Surgeons. Published by Elsevier Inc. All rights reserved.)
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- 2021
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7. Release notice - Cancer in Young People in Canada Data Tool: latest incidence rates and case counts.
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Xie L, Rahman P, Laverty M, Salibi M, Frechette M, Kaur J, Elkhalifa S, Smith-Lépine OW, Bebawy T, Van Millingen S, and Onysko J
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- Adolescent, Canada epidemiology, Humans, Incidence, Registries, Neoplasms epidemiology
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- 2021
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8. Trends in paediatric cancer survival in Canada, 1992 to 2017.
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Ellison LF, Xie L, and Sung L
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- Adolescent, Canada epidemiology, Child, Child, Preschool, Cohort Studies, Databases, Factual, Female, Humans, Infant, Infant, Newborn, Male, Registries, Survival Analysis, Cancer Survivors statistics & numerical data, Mortality trends, Neoplasms mortality
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Background: While impressive gains in childhood cancer survival have been reported both in Canada and internationally, it has been almost 15 years since the last comprehensive evaluation of Canadian data., Data and Methods: Data are from the population-based Canadian Cancer Registry, record-linked to the Canadian Vital Statistics Death database. Children aged 0 to 14 diagnosed with new primary malignant cancers from 1992 to 2017 in Canada except Quebec were included. Overall survival was measured using observed survival proportions (OSPs). Estimates for the 2013-to-2017 period were predicted using the period method; otherwise, the cohort method was used., Results: For the 2013-to-2017 period, five-year OSPs were at least 90% for 10 of 24 individual cancer groups or subgroups reported. Survival was highest for thyroid carcinomas (100%) and Hodgkin lymphomas (99%) and lowest for other gliomas (42%). A significant increase in the five-year OSP from the 1992-to-1996 period (77%) to the 2013-to-2017 period (84%) was observed for all childhood cancers combined, but not since the 2003-to-2007 period. The greatest increase was for chronic myeloproliferative diseases (35.4 percentage points); for lymphoid leukemias, survival increased from 85% to 93%. Survival was relatively poor at baseline for hepatic tumours, malignant bone tumours, and soft tissue and other extraosseous sarcomas, and it remained virtually unchanged. Once children survived five years, the probability of surviving another five years exceeded 95% across most diagnoses., Discussion: Significant improvements in both short- and long-term paediatric cancer survival have been made in Canada since the early to mid-1990s. These findings are clinically meaningful and are likely to be reassuring to families.
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- 2021
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9. DOMESTIC RADON EXPOSURE AND CHILDHOOD LEUKAEMIA AND LYMPHOMA: A POPULATION-BASED STUDY IN CANADA.
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Chen J and Xie L
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- Air Pollutants, Radioactive analysis, Air Pollution, Indoor analysis, Canada epidemiology, Child, Child, Preschool, Female, Humans, Incidence, Infant, Leukemia etiology, Leukemia pathology, Lymphoma etiology, Lymphoma pathology, Male, Neoplasms, Radiation-Induced etiology, Neoplasms, Radiation-Induced pathology, Radiation Monitoring methods, Radon analysis, Risk Factors, Air Pollutants, Radioactive adverse effects, Air Pollution, Indoor adverse effects, Leukemia epidemiology, Lymphoma epidemiology, Neoplasms, Radiation-Induced epidemiology, Radiation Exposure adverse effects, Radon adverse effects
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In this paper, we revisit the possibility, first raised using a data set collected in the 1970s, that there is a link between average radon concentrations and the incidence of childhood leukaemia and lymphoma in Canada. Following the launch of the National Radon Program in 2007, Health Canada completed a long-term radon survey in 33 census metropolitan areas (CMAs), which covers about 70% of the Canadian population. We used this data, together with leukaemia and lymphoma incidence rates among children (0-14 years of age) in the past decade (2006-15), and tried to link the city-level average radon concentrations to the leukaemia and lymphoma incidence rates in 33 major Canadian cities. Analyses were conducted for six subtypes (ALL, AML, CMD, HL, NHL and BL) of leukaemia and lymphoma. Estimated doses to red bone marrow from domestic radon exposure were low and we did not find any association between radon exposure at home and the increased risk for developing leukaemia among children under 15 years of age living in the CMAs. The results indicate a slight positive association for AML among 1-4 year males in CMAs of Peer Group C and NHL among 5-9 year females in CMAs of Peer Group A; however, these should be interpreted with caution owing to the crude exposure assessment and possibilities of other confounding factors., (© Her Majesty the Queen in Right of Canada 2019. Reproduced with the permission of the Minister of Health Canada.)
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- 2019
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10. Canadian breast implant cohort: extended follow-up of cancer incidence.
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Pan SY, Lavigne E, Holowaty EJ, Villeneuve PJ, Xie L, Morrison H, and Brisson J
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- Adolescent, Adult, Canada epidemiology, Cohort Studies, Female, Follow-Up Studies, Humans, Incidence, Middle Aged, Young Adult, Breast Implants adverse effects, Breast Neoplasms epidemiology
- Abstract
Cosmetic breast implants are not associated with increased breast cancer incidence, but variations of risk according to implant characteristics are still poorly understood. As well, the assessment of cancer risk for sites other than breast needs to be clarified. The purpose of this study was to fill these research gaps. This study presents an extended analysis of 10 more years of follow-up of a large Canadian cohort of women who received either cosmetic breast implants (n = 24,558) or other cosmetic surgery (15,893). Over 70% of the implant cohort was followed for over 20 years. Cancer incidence among implant women was compared to those of controls using multivariate Poisson models and the general female population using the standardized incidence ratios (SIRs). Women with breast implants had reduced rates of breast and endometrial cancers compared to other surgery women. Subglandular implants were associated to a reduced rate of breast cancer compared to submuscular implants [incidence rate ratio (IRR) = 0.78, 95% confidence interval (CI) = 0.63-0.96] and this reduction persisted over time. We observed a sevenfold increased rate (IRR = 7.36, 95% CI = 1.86-29.12) of breast cancer in the first 5 years after the date of surgery for polyurethane-coated subglandular implant women but this IRR decreased progressively over time (p value for trend = 0.02). We also observed no increased risk of rarer forms of cancer among augmented women. A reduction in breast cancer incidence was observed for women with subglandular implants relative to women with submuscular implants. Possible increase of breast cancer incidence shortly after breast augmentation with polyurethane implants needs to be verified., (Copyright © 2012 UICC.)
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- 2012
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11. Do breast implants adversely affect prognosis among those subsequently diagnosed with breast cancer? Findings from an extended follow-up of a Canadian cohort.
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Lavigne E, Holowaty EJ, Pan SY, Xie L, Villeneuve PJ, Morrison H, and Brisson J
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- Adult, Breast Neoplasms pathology, Canada epidemiology, Cohort Studies, Female, Follow-Up Studies, Humans, Logistic Models, Neoplasm Staging, Prognosis, Proportional Hazards Models, Breast Implants adverse effects, Breast Neoplasms mortality
- Abstract
Background: Cosmetic breast implants may impair the ability to detect breast cancers. The aims of this study were to examine whether implants and implant characteristics are associated with more advanced breast tumors at diagnosis and poorer survival., Methods: Study population includes all invasive breast cancer cases diagnosed during follow-up of the large Canadian Breast Implant Cohort. A total of 409 women with cosmetic breast implants and 444 women with other cosmetic surgery were diagnosed with breast cancer. These women were compared for stage at diagnosis using multinomial logistic regression models. Cox proportional hazards regression models were used for breast cancer-specific mortality analyses. Comparisons were also conducted according to implant characteristics., Results: Compared with women with other cosmetic surgery, those with cosmetic breast implants had at later stage breast cancer diagnosis (OR of having stage III/IV vs. stage I at diagnosis: 3.04, 95% confidence interval (CI): 1.81-5.10; P < 0.001). A nonstatistically significant increase in breast cancer-specific mortality rate for women with breast implants relative to surgical controls was observed (HR = 1.32, 95% CI: 0.94-1.83, P = 0.11). No statistically significant differences in stage and breast cancer mortality were observed according to implant characteristics., Conclusions: At diagnosis, breast cancers tended to be at more advanced stages among women with cosmetic breast implants. Breast cancer-specific survival was lower in these women although the reduction did not reach statistical significance., Impact: Further investigations of the effect of breast implants on breast cancer prognosis are warranted., (2012 AACR)
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- 2012
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12. Survival of patients diagnosed with either colorectal mucinous or non-mucinous adenocarcinoma: a population-based study in Canada.
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Xie L, Villeneuve PJ, and Shaw A
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- Adenocarcinoma epidemiology, Adenocarcinoma therapy, Adenocarcinoma, Mucinous epidemiology, Adenocarcinoma, Mucinous therapy, Aged, Canada, Colorectal Neoplasms epidemiology, Colorectal Neoplasms therapy, Female, Humans, Male, Middle Aged, Multivariate Analysis, Neoplasm Staging, Prognosis, Registries, Time Factors, Treatment Outcome, Adenocarcinoma mortality, Adenocarcinoma, Mucinous mortality, Colorectal Neoplasms mortality
- Abstract
Previous studies have shown conflicting results on the prognosis of colorectal mucinous adenocarcinoma. This study compared prognostic characteristics of patients diagnosed with mucinous and non-mucinous adenocarcinomas in a Canadian series. Analyses were based on 165 colorectal mucinous and 1215 non-mucinous adenocarcinoma patients who were registered at the Ottawa Regional Cancer Centre from 1994 to 1997, with follow-up extending to December 31, 2001. Differences in survival were examined using the relative survival analysis and the Cox proportional hazards model. For colon, rectum and both combined, the distribution for age at diagnosis, stage and treatment of patients with mucinous adenocarcinoma was similar to that of non-mucinous patients (all p > or = 0.12). Patients with mucinous histology had fewer well- or moderately-differentiated tumours than non-mucinous patients (all p < 0.01). Overall, no statistically significant differences were noted in 5-year relative survival between mucinous and non-mucinous carcinoma for colon, rectum and their combination (p > or = 0.35 for each). However, when the stages were considered separately, patients with stage III mucinous carcinoma had worse survival than patients with non-mucinous carcinoma for both sites. Multivariate analysis of combined data for colon and rectal cancers indicated that independent significant prognostic factors were stage for mucinous, with age and grade as well as stage for non-mucinous carcinoma. In conclusion, no significant differences in stage distribution and overall survival were found between mucinous and non-mucinous patients for colorectal cancer.
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- 2009
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13. Association of fatty acid desaturase gene polymorphisms with blood lipid essential fatty acids and perinatal depression among Canadian women: a pilot study.
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Xie L and Innis SM
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- Canada, Delta-5 Fatty Acid Desaturase, Depression blood, Depression enzymology, Depression, Postpartum blood, Depression, Postpartum enzymology, Depressive Disorder blood, Depressive Disorder enzymology, Female, Humans, Multigene Family, Pilot Projects, Pregnancy, Depression genetics, Depression, Postpartum genetics, Depressive Disorder genetics, Fatty Acid Desaturases genetics, Fatty Acids, Essential blood, Lipids blood, Perinatology, Polymorphism, Genetic, Polymorphism, Single Nucleotide
- Abstract
Aims: The FADS1/FADS2 gene cluster encodes Delta-5 and Delta-6 desaturase, rate-limiting enzymes in metabolism of linoleic (LA) to arachidonic (ARA) and alpha-linolenic to eicosapentaenoic and docosahexaenoic acid (DHA). Single nucleotide polymorphisms (SNPs) in FADS1/FADS2 contribute to variability in blood lipid fatty acids. Altered n-6 and n-3 fatty acids have been related to perinatal depression (PPD)., Methods: We genotyped rs174553, rs99780, rs174575, and rs174583 in FADS1/FADS2, analyzed blood lipid fatty acids and assessed PPD risk as an Edinburgh Postnatal Depression Scale (EPDS) score > or =10 for 69 pregnant women., Results: 21, 12 and 15% women had an EPDS score > or =10 at 36 weeks' gestation, 2 and 6 months postpartum, respectively. Quantitative trait analysis showed an association between rs174575 and PPD risk at 36 weeks' gestation and 6 months postpartum. With haplotype ACCC (major alleles) for rs174553, rs99780, rs174575, rs174583, respectively, as reference, GTCT was positively associated with PPD risk at 36 weeks' gestation, p = 0.028, and higher LA and lower ARA in plasma (p = 0.0001, p < 0.0001) and RBC ethanolamine phospholipids (p = 0.007, p = 0.005)., Conclusions: We show that SNPs in FADS1/FADS2 are associated with higher blood lipid LA and lower ARA and PPD risk., (Copyright 2010 S. Karger AG, Basel.)
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- 2009
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14. Effect of raloxifene after recombinant teriparatide [hPTH(1-34)] treatment in postmenopausal women with osteoporosis.
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Adami S, San Martin J, Muñoz-Torres M, Econs MJ, Xie L, Dalsky GP, McClung M, Felsenberg D, Brown JP, Brandi ML, and Sipos A
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- Aged, Australia, Canada, Europe, Female, Femur Neck chemistry, Femur Neck drug effects, Humans, Lumbar Vertebrae chemistry, Lumbar Vertebrae drug effects, United States, Bone Density drug effects, Bone Density Conservation Agents administration & dosage, Osteoporosis, Postmenopausal drug therapy, Raloxifene Hydrochloride administration & dosage, Teriparatide administration & dosage
- Abstract
Unlabelled: Loss of bone mineral density occurs after discontinuation of teriparatide, if no subsequent treatment is given. Sequential raloxifene prevented rapid bone loss at lumbar spine and further increased bone mineral density (BMD) at femoral neck, whether raloxifene was started immediately or after a one-year delay following teriparatide treatment., Introduction: We compared the sequential effects of raloxifene treatment with a placebo on teriparatide-induced increases in bone mineral density (BMD). A year of open-label raloxifene extended the study to assess the response with and without delay after discontinuation of teriparatide., Methods: Following a year of open-label teriparatide 20 mug/day treatment, postmenopausal women with osteoporosis were randomly assigned to raloxifene 60 mg/day (n = 157) or a placebo (n = 172) for year 2, followed by a year of open-label raloxifene. BMD was measured by dual energy x-ray absorptiometry., Results: The raloxifene and placebo groups showed a decrease in lumbar spine (LS) BMD in year 2 for raloxifene and placebo groups (-1.0 +/- 0.3%, P = 0.004; and -4.0 +/- 0.3%, P < 0.001, respectively); the decrease was less with raloxifene (P < 0.001). Open-label raloxifene treatment reversed the LS BMD decrease with a placebo, resulting in similar decreases 2 years after randomization (-2.6 +/- 0.4% (raloxifene-raloxifene) and -2.7 +/- 0.4% (placebo-placebo). At study end, LS and femoral neck (FN) BMD were higher than pre-teriparatide levels, with no significant differences between the raloxifene-raloxifene and placebo-raloxifene groups, respectively (LS: 6.1 +/- 0.5% vs. 5.1 +/- 0.5%; FN: 3.4 +/- 0.6% vs. 3.0 +/- 0.5%)., Conclusion: Sequential raloxifene prevented rapid bone loss at the LS and increased FN BMD whether raloxifene was started immediately or after a one-year delay following teriparatide treatment.
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- 2008
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15. Survival patterns for the top four cancers in Canada: the effects of age, region and period.
- Author
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Ugnat AM, Xie L, Semenciw R, Waters C, and Mao Y
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- Adolescent, Adult, Age Factors, Aged, Aged, 80 and over, Canada epidemiology, Female, Humans, Male, Middle Aged, Prognosis, Sex Factors, Survival Analysis, Breast Neoplasms epidemiology, Breast Neoplasms pathology, Colorectal Neoplasms epidemiology, Colorectal Neoplasms pathology, Lung Neoplasms epidemiology, Lung Neoplasms pathology, Prostatic Neoplasms epidemiology, Prostatic Neoplasms pathology, SEER Program statistics & numerical data
- Abstract
This study examined the variations in survival rates (1989-1991) and the trends (1969-1991), by sex, age and province, for patients diagnosed with breast, colorectal, lung or prostate cancer in Canada and compared the Canadian rates with those of nine American SEER registries. Five-year age-standardized relative survival rates (ASRs) were calculated, and the trends were estimated from variance-weighted linear regression of the ASRs for five periods of diagnosis (1969-1973, 1974-1978, 1979-1983, 1984-1988 and 1989-1991). In 1989-1991, the ASR varied among provinces for each cancer except female colorectal cancer. The lowest survival rates were observed in the youngest patients (15-44) for breast and prostate cancers, and in the oldest patients (75-99) of both sexes for lung and colorectal cancers. Over the five periods, a major trend toward improved survival was observed for breast, prostate and colorectal cancers (P<0.008), whereas no changes were seen for lung cancer. The ASRs in the western region were higher than in the Atlantic region over time (P<0.02) for each cancer. From the third period onward, the ASRs for Canadian patients with lung cancer were similar to those for the US patients and lower than for Canadian patients with breast, prostate or colorectal cancer. The observed increases in ASR for breast and prostate cancer are likely due to the increased use of screenings and the improved treatment modalities.
- Published
- 2005
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16. The impending Canadian prostate cancer epidemic.
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Morrison HI, MacNeill IB, Miller D, Levy I, Xie L, and Mao Y
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- Age Distribution, Aged, Canada epidemiology, Forecasting, Humans, Incidence, Male, Middle Aged, Population Surveillance, Prostatic Neoplasms mortality, Regression Analysis, Prostatic Neoplasms epidemiology
- Abstract
Purpose: To model and forecast prostate cancer incidence and mortality in Canada to the year 2016., Methods: Bivariate multiplicative models of prostate cancer incidence and mortality for Canadian men aged 45 years or older, linear in time and Weibull in age, were fitted using weighted non-linear regression., Results: The number of incident cases of prostate cancer is forecast to increase from 11,355, observed in 1990, to 26,900 by the year 2010 and to 35,200 by the year 2016. The number of deaths are estimated to climb from 3,424, observed in 1991, to an estimated 6,300 by the year 2010, and to 7,800 by the year 2016., Conclusions: The dramatic increase in prostate cancer rates with age, coupled with the expected large increase in the elderly Canadian male population and steadily increasing prostate cancer incidence rates will produce very large increases in the number of men who will have prostate cancer over the next 20 years. This has important implications for health care delivery in the future.
- Published
- 1995
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