Hunt Steven C, Chen Wei, Gardner Jeffrey P, Kimura Masayuki, Srinivasan Sathanur R, Eckfeldt John H, Berenson Gerald S, Aviv Abraham
Cardiovascular Genetics Division, University of Utah School of Medicine, Salt Lake City, UT, USA (NHLBI Family Heart Study).
Aging Cell. 2008 Aug;7(4):451-8. doi: 10.1111/j.1474-9726.2008.00397.x. Epub 2008 May 2.
Leukocyte telomere length (LTL) is ostensibly a bio-indicator of human aging. Here we report that African Americans have longer LTL than whites. We studied cross-sectionally 2453 individuals from the National Heart, Lung, and Blood Institute (NHLBI) Family Heart Study (age = 30-93 years) and the Bogalusa Heart Study (age = 19-37 years), comprising 1742 whites and 711 African Americans. We measured LTL by Southern blots of the terminal restriction fragments length. In 234 participants, telomere repeats were also measured by quantitative polymerase chain reaction (qPCR). Adjusted for age and body mass index (BMI), the respective leukocyte telomere lengths (mean +/- SEM) were considerably longer in African Americans than in whites both in the Family Heart Study (7.004 +/- 0.033 kb vs. 6.735 +/- 0.024 kb, p < 0.0001) and the Bogalusa Heart Study (7.923 +/- 0.063 kb vs. 7.296 +/- 0.039 kb, p < 0.0001). We confirmed the racial effect on LTL by qPCR (3.038 +/- 0.565 T/S units for African Americans vs. 2.714 +/- 0.487 T/S units for whites, p < 0.001). Cross-sectionally, sex- and BMI-adjusted LTL became shorter with age (range 19-93 years) at a steeper slope in African Americans than in whites (0.029 kb year(-1) vs. 0.020 kb year(-1), respectively, p = 0.0001). We suggest that racial difference in LTL arises from a host of interacting biological factors, including replication rates of hematopoietic stem cells.
白细胞端粒长度(LTL)表面上是人类衰老的生物指标。在此我们报告,非裔美国人的LTL比白人更长。我们对来自美国国立心肺血液研究所(NHLBI)家庭心脏研究(年龄30 - 93岁)和博加卢萨心脏研究(年龄19 - 37岁)的2453名个体进行了横断面研究,其中包括1742名白人及711名非裔美国人。我们通过对末端限制片段长度进行Southern印迹法测量LTL。在234名参与者中,还通过定量聚合酶链反应(qPCR)测量了端粒重复序列。在校正年龄和体重指数(BMI)后,无论是在家庭心脏研究中(7.004±0.033 kb对6.735±0.024 kb,p < 0.0001)还是在博加卢萨心脏研究中(7.923±0.063 kb对7.296±0.039 kb,p < 0.0001),非裔美国人的白细胞端粒长度(平均值±标准误)均显著长于白人。我们通过qPCR证实了种族对LTL的影响(非裔美国人3.038±0.565 T/S单位,白人2.714±0.487 T/S单位,p < 0.001)。横断面研究显示,在校正性别和BMI后,LTL随年龄(19 - 93岁)增长而缩短,非裔美国人的斜率比白人更陡(分别为0.029 kb/年对0.020 kb/年,p = 0.0001)。我们认为LTL的种族差异源于一系列相互作用的生物学因素,包括造血干细胞的复制率。