Tu Wanzhu, Wagner Erin K, Eckert George J, Yu Zhangsheng, Hannon Tamara, Pratt J Howard, He Chunyan
Department of Biostatistics, Indiana University School of Medicine, Indianapolis, Indiana.
Department of Epidemiology, Richard M. Fairbanks School of Public Health, Indiana University, Indianapolis, Indiana.
J Adolesc Health. 2015 Jan;56(1):66-72. doi: 10.1016/j.jadohealth.2014.07.020. Epub 2014 Oct 3.
Previous studies have identified novel genetic variants associated with age at menarche in females of European descent. The pubertal growth effects of these variants have not been carefully evaluated in non-European descent groups. We aimed to examine the effects of 31 newly identified menarche-related single-nucleotide polymorphisms (SNPs) on growth outcomes in African-American (AA) and European-American (EA) children in a prospective cohort.
We analyzed longitudinal data collected from 263 AAs and 338 EAs enrolled between ages 5 and 17 years; the subjects were followed semiannually for an average of 6 years. The associations between the SNPs and growth-related outcomes, including weight, height, and body mass index (BMI), were examined using mixed-effect models.
Longitudinal analyses revealed that 4 (near or in genes VGLL3, PEX2, CA10, and SKOR2) of the 14 menarche-only-related SNPs were associated with changes in weight and BMI in EA and AA (p ≤ .0032), but none of them was associated with changes in height. Of the eight menarche-timing and BMI-related SNPs, none was associated with changes in height, but three (in or near genes NEGR1, ETV5, and FTO) were associated with more rapid increases in weight and/or BMI in EA (p ≤ .0059). Among the nine menarche-timing and height-related SNPs, four (in or near genes ZBTB38, LOC728666, TBX2, and CABLES) were associated with changes in weight or height in EA and AA (p ≤ .0042).
Genetic variants related to age at menarche were found to be associated with various growth parameters in healthy adolescents. The identified associations were often race and sex specific.
先前的研究已经确定了与欧洲裔女性初潮年龄相关的新型基因变异。这些变异对青春期生长的影响尚未在非欧洲裔群体中得到仔细评估。我们旨在研究31个新发现的与初潮相关的单核苷酸多态性(SNP)对非裔美国(AA)和欧裔美国(EA)儿童生长结果的影响,该研究为一项前瞻性队列研究。
我们分析了从263名AA儿童和338名EA儿童中收集的纵向数据,这些儿童年龄在5至17岁之间;对这些受试者每半年进行一次随访,平均随访6年。使用混合效应模型检查SNP与生长相关结果(包括体重、身高和体重指数(BMI))之间的关联。
纵向分析显示,14个仅与初潮相关的SNP中有4个(位于或临近基因VGLL3、PEX2、CA10和SKOR2)与EA和AA儿童的体重和BMI变化相关(p≤0.0032),但均与身高变化无关。在8个与初潮时间和BMI相关的SNP中,没有一个与身高变化相关,但有3个(位于或临近基因NEGR1、ETV5和FTO)与EA儿童体重和/或BMI的更快增加相关(p≤0.0059)。在9个与初潮时间和身高相关的SNP中,有4个(位于或临近基因ZBTB38、LOC728666、TBX2和CABLES)与EA和AA儿童的体重或身高变化相关(p≤0.0042)。
发现与初潮年龄相关的基因变异与健康青少年的各种生长参数相关。所确定的关联通常具有种族和性别特异性。