Department of Epidemiology, University of Michigan School of Public Health, Ann Arbor, Michigan, USA.
Eunice Kennedy Shriver National Institute of Child Health and Development, Rockville, Maryland, USA.
Am J Hum Biol. 2022 Jan;34(1):e23596. doi: 10.1002/ajhb.23596. Epub 2021 Mar 15.
Leukocyte telomere length (LTL) may be involved in the etiology of the metabolic syndrome (MetS). We examined the associations of LTL with MetS and its components among Mesoamerican children and their adult parents, in a region where MetS prevalence is high.
We conducted a cross-sectional study of 151 children aged 7-12 years and 346 parents from the capitals of Belize, Honduras, Nicaragua, Costa Rica, Panama, and Chiapas State, Mexico. We quantified LTL by qPCR on DNA extracted from whole blood. In children, we created an age- and sex-standardized metabolic risk score using waist circumference (WC), the homeostasis model of insulin resistance (HOMA-IR), blood pressure, serum high-density lipoprotein (HDL) cholesterol, and serum triglycerides. In adults, MetS was defined according to the National Cholesterol Education Program's Adult Treatment Panel III definition. We estimated mean differences in metabolic risk score and prevalence ratios of MetS across quartiles of LTL using multivariable-adjusted linear and Poisson regression models, respectively.
In children, every 1 LTL z-score was related to an adjusted 0.05 units lower (95% CI: -0.09, -0.02, P = 0.005) MetS risk score, through WC, HOMA-IR, and HDL. Among adults, LTL was not associated with MetS prevalence; however, every 1 LTL z-score was associated with an adjusted 34% lower prevalence of high fasting glucose (95% CI: 3%, 55%, p = .03).
Among Mesoamerican children, LTL is associated with an improved metabolic profile; among adults, LTL is inversely associated with the prevalence of high fasting glucose.
白细胞端粒长度(LTL)可能与代谢综合征(MetS)的病因有关。我们在中美洲一个 MetS 患病率较高的地区,研究了 LTL 与 MetS 及其各成分之间的关系。
我们对来自伯利兹、洪都拉斯、尼加拉瓜、哥斯达黎加、巴拿马和墨西哥恰帕斯州首府的 151 名 7-12 岁儿童和 346 名家长进行了横断面研究。我们使用 qPCR 从全血提取的 DNA 定量 LTL。在儿童中,我们使用腰围(WC)、胰岛素抵抗的稳态模型(HOMA-IR)、血压、血清高密度脂蛋白(HDL)胆固醇和血清甘油三酯,创建了一个年龄和性别标准化的代谢风险评分。在成年人中,根据国家胆固醇教育计划成人治疗小组 III 定义来确定 MetS。我们使用多变量调整线性和泊松回归模型分别估计了 LTL 四分位数的代谢风险评分的平均差异和 MetS 的患病率比。
在儿童中,LTL 每增加 1 个 Z 分数,与调整后的 MetS 风险评分降低 0.05 个单位(95%CI:-0.09,-0.02,P=0.005)有关,这通过 WC、HOMA-IR 和 HDL 来实现。在成年人中,LTL 与 MetS 的患病率无关;然而,LTL 每增加 1 个 Z 分数,与调整后的空腹高血糖患病率降低 34%有关(95%CI:3%,55%,p=0.03)。
在中美洲儿童中,LTL 与改善的代谢特征有关;在成年人中,LTL 与空腹高血糖的患病率呈负相关。