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诊断前白细胞端粒长度与卵巢癌风险

Prediagnosis Leukocyte Telomere Length and Risk of Ovarian Cancer.

作者信息

Yang Meng, Prescott Jennifer, Poole Elizabeth M, Rice Megan S, Kubzansky Laura D, Idahl Annika, Lundin Eva, De Vivo Immaculata, Tworoger Shelley S

机构信息

Department of Nutrition, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.

Channing Division of Network Medicine, Brigham and Women's Hospital/Harvard Medical School, Boston, Massachusetts.

出版信息

Cancer Epidemiol Biomarkers Prev. 2017 Mar;26(3):339-345. doi: 10.1158/1055-9965.EPI-16-0466. Epub 2017 Feb 16.

Abstract

The associations between telomere length and cancer risk are equivocal, and none have examined the association between prediagnosis leukocyte telomere length (LTL) and the risk of developing ovarian cancer. We prospectively measured LTL collected from 442 ovarian cancer cases and 727 controls in the Nurses' Health Studies and the Northern Sweden Health and Disease Study. Cases were matched to one or two controls on age, menopausal status, and date of blood collection. Odds ratios (OR) and 95% confidence intervals (CI) were estimated using conditional logistic regression. LTL was measured a median of 9.5 years before ovarian cancer diagnosis among cases. We observed a decreased risk of ovarian cancer with longer LTL. In multivariable models, women in the top quartile of LTL had an OR for ovarian cancer of 0.67 (95% CI, 0.46-0.97) compared with those in the bottom quartile. Inverse associations were stronger for nonserous cases (OR = 0.55, 95% CI, 0.33-0.94) and rapidly fatal cases (i.e., cases who died within 3 years of diagnosis; OR = 0.55, 95% CI, 0.32-0.95). Our prospective findings suggest that longer circulating LTL may be associated with a lower ovarian cancer risk, especially for nonserous and rapidly fatal cases. The evaluation of LTL in relation to ovarian cancer risk by tumor subtypes is warranted in larger prospective studies. Prediagnosis LTL may reflect an early event in the ovarian cancer development and could serve as a biomarker to predict future risk. .

摘要

端粒长度与癌症风险之间的关联尚不明确,且尚无研究探讨癌症诊断前白细胞端粒长度(LTL)与卵巢癌发生风险之间的关联。我们在护士健康研究和瑞典北部健康与疾病研究中,对442例卵巢癌病例和727例对照的LTL进行了前瞻性测量。病例根据年龄、绝经状态和采血日期与一至两个对照进行匹配。使用条件逻辑回归估计比值比(OR)和95%置信区间(CI)。病例组在卵巢癌诊断前中位数9.5年时测量LTL。我们观察到LTL越长,卵巢癌风险越低。在多变量模型中,LTL处于最高四分位数的女性患卵巢癌的OR为0.67(95%CI,0.46 - 0.97),而处于最低四分位数的女性为对照。非浆液性病例(OR = 0.55,95%CI,0.33 - 0.94)和快速致命病例(即诊断后3年内死亡的病例;OR = 0.55,95%CI,0.32 - 0.95)的负相关更强。我们的前瞻性研究结果表明,循环LTL越长可能与卵巢癌风险越低相关,尤其是对于非浆液性和快速致命病例。在更大规模的前瞻性研究中,有必要按肿瘤亚型评估LTL与卵巢癌风险的关系。癌症诊断前的LTL可能反映了卵巢癌发生过程中的早期事件,并可作为预测未来风险的生物标志物。

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Depression and telomere length: A meta-analysis.抑郁症与端粒长度:一项荟萃分析。
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