Mary Ann and J. Milburn Smith Child Health Research Program, Department of Pediatrics, Northwestern University Feinberg School of Medicine and Children's Memorial Hospital and Children's Memorial Research Center, Chicago, Illinois 60614, USA.
J Clin Endocrinol Metab. 2010 Apr;95(4):1644-52. doi: 10.1210/jc.2009-1726. Epub 2010 Feb 10.
Adipokines have been linked to bone phenotypes recently, but with conflicting results. Few such studies have been conducted in adolescents.
The aim of the study was to examine the associations of adiponectin and leptin with multiple bone phenotypes in Chinese adolescents and estimate the genetic contribution to these associations.
This was a cross-sectional study conducted in rural China.
A total of 675 males and 575 females aged 13-21 yr were included.
Fat mass (FM), lean mass (LM), bone area (BA), bone mineral content (BMC), cross-sectional area (CSA), and section modulus (SM) were measured by dual-energy x-ray absorptiometry. Plasma adipokine concentration was determined using sandwich immunoassays.
Adiponectin was inversely associated with all BMCs in males (P < 0.01), but not in females, after adjusting for LM, body weight, or BMI singly, or for LM and FM simultaneously. No such relationships were observed for CSA or SM in both genders. Leptin was inversely associated with all BAs, total-hip BMC, CSA, and SM in both genders, when adjusting for body weight or BMI. These associations, except for whole-body BA and lumbar spine BA in females, disappeared when simultaneously adjusting for LM and FM. By Cholesky decomposition models using twin design, significant genetic correlations were detected between adiponectin and total-hip BMC in males and between leptin and total-hip BMC in both genders.
We demonstrated that adiponectin and leptin were inversely associated with adolescent bone phenotypes but showed differential associations by gender, type of bone phenotypes, and adjustment of FM. This study also suggested that adipokines and bone phenotypes may share a common set of genes.
脂肪因子与骨表型最近有关联,但结果相互矛盾。在青少年中进行的此类研究很少。
本研究旨在检测中国人青少年中脂联素和瘦素与多种骨表型的关联,并估计这些关联的遗传贡献。
这是在中国农村进行的一项横断面研究。
共纳入 675 名男性和 575 名 13-21 岁的女性。
采用双能 X 射线吸收法测量脂肪量 (FM)、瘦体重 (LM)、骨面积 (BA)、骨矿物质含量 (BMC)、横截面积 (CSA)和截面模数 (SM)。使用夹心免疫测定法测定血浆脂联素浓度。
在调整 LM、体重或 BMI 单项或 LM 和 FM 同时调整后,脂联素与男性所有 BMC 呈负相关(P<0.01),但在女性中则没有。在两性中,CSA 或 SM 均未观察到这种关系。瘦素与两性所有 BA、全髋 BMC、CSA 和 SM 呈负相关,当调整体重或 BMI 时。这些关联在同时调整 LM 和 FM 时,除了女性的全身体 BA 和腰椎 BA 之外,均消失了。使用双胞胎设计的 Cholesky 分解模型,检测到脂联素与男性全髋 BMC 之间以及瘦素与两性全髋 BMC 之间存在显著的遗传相关性。
我们表明,脂联素和瘦素与青少年骨表型呈负相关,但在性别、骨表型类型和 FM 调整方面表现出不同的关联。本研究还表明,脂肪因子和骨表型可能共享一组共同的基因。