代谢性疾病的家族风险;及时筛选血管内皮健康的一个参数

Preeti Kanawjia, S. Tiwari, M. Bajpai
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引用次数: 0

摘要

目的:探讨健康超重、肥胖和非肥胖人群血管内皮健康与代谢紊乱家族风险的相关性。研究设计:病例对照(先导)研究。研究地点和时间:研究在K.G.M.U生理学系心血管生理实验室进行。方法:2009年1月至2010年2月为病例和对照组。30名超重/肥胖健康受试者(BMI >= 25 kg/m2和/或WHR(女性>0.85);男性>1)和30名非肥胖健康受试者(BMI< 25 kg/m2和/或WHR(女性<0.85;男性<1),排除继发性血流量异常的受试者。血管内皮健康状况通过反应性充血反应进行评估,该反应性充血反应是通过受试者前臂的阻抗容积描记术测量的。同时测定空腹血糖和血脂。结果:经生化指标比较,两组均有脂质紊乱。VLDL(对照组21.84±9.68,病例29.01±16.83)、TG(对照组101.22±-43.33;Case145.21±84.02)(p=0.013)。VLDL和TG紊乱者15例(6例+ 9例对照)(P=0.371), 14例(5例+ 9例对照)(P=0.222),组间差异无统计学意义。闭塞后1、2、3、5、7、9 min组间反应性充血差异无统计学意义。两组均在2分钟出现充血反应高峰。虽然糖尿病、冠状动脉疾病和/或高血压一级亲属的独立家族史与2 min时的% RH有显著相关性(P =0.049),但在分组探索中,未见显著相关性。结论:人体测量不良与血脂异常无明显相关性,反之亦然。RH反应升高与阳性家族风险相关,可能是由于高胰岛素血症和/或一些尚未解释的原因,但不仅仅是紊乱的人体测量(BMI和WHR)的附加后遗症。根据我们的研究结果,我们得出结论,在具有阳性危险因素家族史的受试者中,似乎是有利的反应,即充血反应升高,可能是血管系统屈服于炎症侮辱之前的最后一根逃生反应。因此,一些尚未解释的原因可能被怀疑是不良结果,因此可以通过改变生活方式或药物干预及时加以纠正。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Family Risk of Metabolic Disorder; A Parameter for Timely Screening of Vascular Endothelial Health
Aim: To study the correlation of vascular endothelial health with family risk of metabolic disorders, in healthy overweight, obese and non obese subjects. Study Design: A case-control (pilot) study. Place and Duration of Study: The study was conducted in Cardiovascular Physiology lab, Department of Physiology, K.G.M.U Methods: Cases and controls comprised from January 2009 to February 2010. of 30 overweight / obese healthy subjects (BMI >= 25 kg/m2 and/or WHR (female>0.85; male>1) and 30 non-obese healthy subjects respectively (BMI< 25 kg/m2 and/or WHR (female<0.85; male<1) excluding subjects with secondary cause of abnormal blood flow. Vascular endothelial health was assessed via reactive hyperemic response measured via impedance plethysmography in the subject’s forearm. Fasting plasma glucose and serum lipid profile was also done. Results: On comparison of biochemical variables, lipid derangement was recorded in both the groups. Significant difference in VLDL (control 21.84±9.68, case 29.01±16.83) (p=0.048) and TG (control 101.22±-43.33; case145.21±84.02) (p=0.013), could be seen. VLDL & TG was deranged in 15 (6 cases + 9 controls) (P=0.371) and 14 (5 cases + 9 controls) (P=0.222) subjects respectively with no inter-group significant statistical difference. Inter-group reactive hyperemia at 1, 2, 3, 5, 7, 9 min post occlusion time showed no significant difference. Peak hyperemic response was seen at 2 minutes in both the groups. Though independent family history in first degree relatives of diabetes, coronary artery disease and/or hypertension showed a significant association with % RH at 2 min. (P =0.049), yet in group wise exploration, no significant association was seen. Conclusion: Adverse anthropometry is universally not associated with deranged lipid profile and vice versa. Raised RH response associated with positive family risk could be either due to hyperinsulinemia and/or some yet undeciphered cause but not solely as add-on sequelae of deranged anthropometry (BMI & WHR). In the light of our findings, we conclude that what seems as a favourable response i.e. a raised hyperemic response in subjects with a positive family history of risk factors, may be last ditch escape response before the vascular system succumbs to the inflammatory insult. Some yet undeciphered causes could thus be suspected of an adverse outcome and thus accordingly timely modified by lifestyle modifications or pharmacological interventions.
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