孤立性生长激素缺乏导致的矮小儿童心血管疾病风险的综合评估:一项病例对照研究

IF 1
Saniya Gupta, Devi Dayal, Manoj Kumar Rohit, Atit A Gawalkar, Kumar Manish Raj, Savita Verma Attri, Naresh Sachdeva, Harvinder Kaur
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引用次数: 1

摘要

目的:成人生长激素缺乏症(GHD)与心血管发病率和死亡率增加相关。虽然患有GHD的儿童也被认为在早期就有类似的心血管疾病(CVD)风险,但现有的儿童数据很少。我们的目的是确定孤立性GHD (IGHD)儿童的各种CVD风险参数。方法:在印度北部的一家三级保健中心进行了一项横断面病例对照研究,比较了20名5-15岁的IGHD儿童及其年龄和性别匹配的健康对照者的各种生长学、生化和超声心动图参数。结果:IGHD患儿和对照组的平均年龄相似(10.5±2.6岁vs 9.9±2.7岁,p=0.48)。IGHD患儿腰臀比(p=0.01)、总胆固醇(p=0.02)、非高密度脂蛋白-胆固醇(p=0.02)、血清同型半胱氨酸(p= 0.05)均显著增高。结论:IGHD患儿表现出多项生化和心脏参数异常,可能与晚年CVD风险增加有关。需要更广泛的研究,包括年幼的IGHD儿童,来确定可检测到心血管疾病风险的较低年龄。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comprehensive assessment of cardiovascular disease risk in children with short stature due to isolated growth hormone deficiency: a case-control study.

Objectives: Growth hormone deficiency (GHD) in adults is associated with an increased risk of cardiovascular morbidity and mortality. Although children with GHD are also believed to have a similar cardiovascular disease (CVD) risk beginning at an early age, the available data in children is scarce. We aimed to determine the various CVD risk parameters in children with isolated GHD (IGHD).

Methods: A cross-sectional case-control study was conducted at a tertiary care centre in North India comparing various auxological, biochemical, and echocardiographic parameters between 20 IGHD children aged 5-15 years and their age and sex-matched healthy controls.

Results: The mean age of children with IGHD and controls was similar (10.5 ± 2.6 yr vs. 9.9 ± 2.7 yr, p=0.48). Children with IGHD had significantly higher waist-hip-ratio (p=0.01), total cholesterol (p=0.02), non-high-density lipoprotein-cholesterol (p=0.02), serum homocysteine (p<0.001), C-reactive protein (CRP) (p=0.01) and pro-brain natriuretic peptide (pro-BNP) (p=0.04) levels as compared to healthy controls. Left ventricular mass (LVM) and interventricular septal thickness were significantly lower (p=0.04; p=0.02) in IGHD children. Correlation analysis showed that pro-BNP and CRP levels had negative correlation (p<0.001, r=-0.70; and p=0.04, r=-0.44, respectively) and LVM had a positive correlation (p=0.02, r=0.53) with height SDS among IGHD children.

Conclusions: Children with IGHD showed abnormalities in several biochemical and cardiac parameters that may be associated with an increased CVD risk in later life. More extensive studies, including younger children with IGHD, are needed to determine the lower ages at which the CVD risk is detectable.

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