Growth and Body Composition Lab, Center for Investigation in Pediatrics, Faculty of Medical Sciences (FCM), State University of Campinas, Campinas, SP, Brazil.
Early Hum Dev. 2012 Feb;88(2):99-102. doi: 10.1016/j.earlhumdev.2011.07.014. Epub 2011 Jul 29.
Turner syndrome (TS) patients have an increased risk of weight gain and metabolic syndrome. To date, it is unknown what factors are involved in this metabolic process, even though it is recognized that TS patients are frequently born small-for-gestational age. The aim of this study was to evaluate the correlation between lipid and glucose profiles with being overweight and birth weight and length in TS patients.
This was a cross-sectional study.
Serum glucose, insulin (HOMA-IR), total cholesterol, and triglycerides were measured in 64 patients with TS. Data regarding birth weight and length and current body mass index (BMI) were also evaluated.
Total cholesterol showed a significant negative correlation with birth weight and a positive correlation with BMI; triglycerides showed significant negative correlation with birth weight and length and a positive correlation with BMI; and HOMA-IR showed a significant negative correlation with birth weight and length. Low birth weight and a high BMI were predictive for 28% of total cholesterol and triglycerides; and low birth weight for 22% of HOMA-IR.
Lipid profile was correlated with a high current BMI and low birth weight and length in TS patients and glucose profile only with low birth weight. Thus far, growth retardation may play a role in metabolic derangements in this group of patients, being considered another example of fetal programming.
特纳综合征(TS)患者体重增加和代谢综合征的风险增加。迄今为止,尽管人们已经认识到 TS 患者通常出生时体重小于胎龄,但尚不清楚哪些因素参与了这一代谢过程。本研究旨在评估 TS 患者的脂质和葡萄糖谱与超重和出生体重及长度之间的相关性。
这是一项横断面研究。
测量了 64 例 TS 患者的血清葡萄糖、胰岛素(HOMA-IR)、总胆固醇和甘油三酯。还评估了与出生体重和长度以及当前体重指数(BMI)相关的数据。
总胆固醇与出生体重呈显著负相关,与 BMI 呈正相关;甘油三酯与出生体重和长度呈显著负相关,与 BMI 呈正相关;HOMA-IR 与出生体重和长度呈显著负相关。低出生体重和高 BMI 可预测总胆固醇和甘油三酯的 28%;低出生体重可预测 HOMA-IR 的 22%。
脂质谱与 TS 患者当前的高 BMI 和低出生体重及长度相关,而葡萄糖谱仅与低出生体重相关。到目前为止,生长迟缓可能在这组患者的代谢紊乱中起作用,被认为是胎儿编程的另一个例子。