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母体和脐带血白细胞端粒长度的种族差异及其相关性。

Racial differences in maternal and umbilical cord blood leukocyte telomere length and their correlations.

作者信息

Weber Kari A, Heaphy Christopher M, Joshu Corinne E, Lu Jiayun, Rohrmann Sabine, Bienstock Jessica L, Agurs-Collins Tanya, Meeker Alan K, Platz Elizabeth A

机构信息

Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, 615 N. Wolfe Street, Baltimore, MD, 21205, USA.

Department of Pathology, Johns Hopkins University School of Medicine, 600 N. Wolfe Street, Baltimore, MD, 21287, USA.

出版信息

Cancer Causes Control. 2018 Aug;29(8):759-767. doi: 10.1007/s10552-018-1054-8. Epub 2018 Jul 6.

Abstract

PURPOSE

Telomere length at birth sets the baseline for telomere shortening and may influence adult disease risk like cancer. Telomere length is heritable, but may also be a marker of exposures in utero, including those influencing racial differences in risk. We examined racial differences in telomere length in maternal and umbilical cord blood from male neonates, and maternal-neonate correlations to generate hypotheses.

METHODS

Black and white pregnant women were recruited in 2006-2007 and followed to postpartum. Data came from questionnaires and medical records. Relative telomere length was measured by qPCR in leukocyte DNA. We estimated mean telomere length in mothers and neonates (n = 55 pairs) using linear regression and maternal-cord blood Spearman correlations, overall and by race.

RESULTS

Black mothers had shorter age- and plate-adjusted telomere length (2.49, 95% CI 2.11-2.86) than whites (2.92, 95% CI 2.63-3.22; p = 0.1) and black neonates had shorter telomere length (2.58, 95% CI 2.16-3.01) than whites (3.13, 95% CI 2.79-3.47; p = 0.1), though not statistically significant. Differences were attenuated after further adjustment for maternal factors. Maternal-cord blood correlations were moderate (r = 0.53, p < 0.0001), and did not differ by race.

CONCLUSION

Telomere length may differ by race at birth due to both inherited and racial differences in maternal factors. This study was for hypothesis generation and results should be followed up in larger studies.

摘要

目的

出生时的端粒长度为端粒缩短设定了基线,并可能影响成人患癌等疾病的风险。端粒长度具有遗传性,但也可能是子宫内暴露情况的一个指标,包括那些影响风险种族差异的因素。我们研究了男性新生儿的母亲和脐带血中端粒长度的种族差异,以及母婴相关性以提出假设。

方法

2006 - 2007年招募了黑人和白人孕妇并随访至产后。数据来自问卷和医疗记录。通过qPCR测量白细胞DNA中的相对端粒长度。我们使用线性回归和母婴脐带血Spearman相关性估计母亲和新生儿(n = 55对)的平均端粒长度,总体及按种族分别进行估计。

结果

黑人母亲经年龄和血小板校正后的端粒长度(2.49,95%置信区间2.11 - 2.86)短于白人母亲(2.92,95%置信区间2.63 - 3.22;p = 0.1),黑人新生儿的端粒长度(2.58,95%置信区间2.16 - 3.01)短于白人新生儿(3.13,95%置信区间2.79 - 3.47;p = 0.1),尽管差异无统计学意义。在进一步调整母亲因素后,差异有所减弱。母婴脐带血相关性为中等(r = 0.53,p < 0.0001),且种族间无差异。

结论

由于母亲因素的遗传和种族差异,出生时端粒长度可能存在种族差异。本研究用于提出假设,结果应在更大规模的研究中进行后续验证。

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