代谢综合征患者甲状腺功能紊乱的模式

A. Ali, A. Deeb, A. Orabi, M. Abdu, A. Gad
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引用次数: 0

摘要

目的:探讨代谢综合征患者甲状腺功能紊乱的规律。方法:本研究对130例代谢综合征患者进行横断面描述性研究。结果:平均年龄57.5岁,女性88例,占67.69%。根据HOMA-IR估计;129例(99.2%)患者存在胰岛素抵抗。亚临床甲状腺功能减退34例(26.15%)。亚临床甲状腺功能减退患者与非亚临床甲状腺功能减退患者之间没有年龄和性别差异,但血脂异常患病率(高甘油三酯,25[73.53%]比33[34.38%],p=0.001)和(低HDL-C, 34[100%]比81[84.38%],p= 0.01)在亚临床甲状腺功能减退患者中分别显著高于非亚临床甲状腺功能减退患者。亚临床甲状腺功能减退患者的平均±SD腰围(138.6 cm±1.4 vs 118.9±9.9,p=0.001)和腰臀比(1.24±0.08 vs 1.098±0.09,p=0.001)均显著高于非亚临床甲状腺功能减退患者。两组间HOMA-IR差异无统计学意义。此外,HOMA-IR与游离甲状腺素(FT4)或促甲状腺激素(TSH)均无显著相关性。TSH与甘油三酯呈显著正相关;R= 0.2, P=0.02,与HDL-C呈负相关;R = -。02年,P = 0.01。TSH与肥胖参数(腰围;R=0.6, P=0.001,腰臀比;R=0.5, P=0.001), FT4与空腹胰岛素呈显著负相关;R= -0.2, 0.04,腰围;R= -0.2, P=0.01与腰臀比;R= -0.3, p =0.002。ROC下面积(95% CI)为0.93 (0.88-0.97),P=0.001,腰围预测亚临床甲状腺功能减退的敏感性为97%,特异性为81%,腰臀比预测亚临床甲状腺功能减退的敏感性为0.86 (0.79-0.91),P=0.001,敏感性为91%,特异性为77%。结论:亚临床甲状腺功能减退在代谢综合征患者中普遍存在。TSH与代谢综合征参数,特别是血脂异常和肥胖指标显著相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pattern of Thyroid Functional Derangements in Patients with Metabolic Syndrome
Aim: To study the pattern of thyroid functional derangements in patients with metabolic syndrome. Methods: The current study was designed as a cross sectional descriptive study of 130 patients with metabolic syndrome. Results: The mean age was 57.5, with 88 [67.69%] females. According to HOMA-IR estimation; 129 (99.2%) of the studied patients were found to have insulin resistance. Subclinical hypothyroidism was diagnosed in 34 (26.15%). There was no age or sex difference between patients with and without subclinical hypothyroidism however a significant higher prevalence of dyslipidemia (high triglyceride, 25[73.53%] vs. 33[34.38%,], p=0.001) and (low HDL-C, 34[100%] VS. 81[84.38%], P=0.01) in patients with compared to without subclinical hypothyroidism respectively. Also, the mean ± SD waist circumference (138.6 cm ± 1.4 vs 118.9 ± 9.9, p=0.001) and waist/hip ratio (1.24 ± 0.08 vs. 1.098 ± 0.09, p= 0.001) were significantly higher in patients with compared to without subclinical hypothyroidism respectively. There was no statistically significant difference between the two groups regarding HOMA-IR. In addition, there was no significant correlation between HOMA-IR and either free thyroxine (FT4) or thyroid stimulating hormone (TSH). However, TSH was significantly positively correlated with triglycerides; R= 0.2, P=0.02 and negatively correlated with HDL-C; R=-.02, P=0.01. There was significant strong positive correlation between TSH and obesity parameters (waist circumference; R=0.6, P=0.001 and waist/hip ratio; R=0.5, P=0.001), while a significant negative correlation was found between FT4 and fasting insulin; R= -0.2, 0.04, waist circumference; R= -0.2, P=0.01 and waist hip ratio; R= -0.3, P=0.002. The area under the ROC (95% CI) was 0.93 (0.88-0.97), P=0.001 for the waist circumference as a predictor of subclinical hypothyroidism with a sensitivity of 97% and specificity of 81%, while that of waist / hip ratio was 0.86 (0.79-0.91), p=0.001, with a sensitivity of 91% and specificity of 77%. Conclusion: Subclinical hypothyroidism is prevalent among patients with metabolic syndrome. TSH is significantly associated with metabolic syndrome parameters particularly dyslipidemia and obesity indicators.
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