Euser Anne M, Dekker Friedo W, Hallan Stein I
Department of Cancer Research and Molecular Medicine, Faculty of Medicine, Norwegian University of Science and Technology, Trondheim, Norway.
Eur J Cardiovasc Prev Rehabil. 2010 Jun;17(3):314-20. doi: 10.1097/HJR.0b013e328331d2c3.
The validity and appropriateness of the metabolic syndrome as a cardiovascular risk factor are increasingly debated, partly because of the lack of a unifying underlying pathophysiological mechanism. Intrauterine growth retardation (low birth weight by sex and gestational length) has been associated with several cardiovascular problems and could be an important underlying risk factor for the metabolic syndrome.
The association between intrauterine growth retardation (from the Norwegian Medical Birth Registry) and the metabolic syndrome in 7435 men and women aged 20-30 years from the population-based HUNT 2 study was studied with logistic regression using fractional polynomial models.
In men, there were significant associations with several of the separate components of the metabolic syndrome: central obesity (exponential, P<0.001), raised triglycerides (negative linear, P = 0.018), reduced HDL-cholesterol (U-shaped, P = 0.086), raised blood pressure (negative linear, P = 0.036), and impaired glucose tolerance (negative linear, P = 0.036). In women, there were significant associations with central obesity (positive linear, P<0.001) and raised blood pressure (negative linear, P = 0.003) but not with the other components. When combining these components into the metabolic syndrome, an exponential association was found in men (P = 0.017), that is, increased risk in patients with high birth weight only. In women, there was no association at all (P = 0.959).
Low birth weight was not associated with the metabolic syndrome at young adult age. Several associations between birth weight and the separate components of the syndrome were found, however, but these associations were partly in different directions.
代谢综合征作为心血管危险因素的有效性和适用性受到越来越多的争议,部分原因是缺乏统一的潜在病理生理机制。宫内生长迟缓(根据性别和孕周划分的低出生体重)与多种心血管问题相关,可能是代谢综合征的一个重要潜在危险因素。
利用分数多项式模型,通过逻辑回归研究了基于人群的HUNT 2研究中7435名20至30岁男性和女性的宫内生长迟缓(来自挪威医学出生登记处)与代谢综合征之间的关联。
在男性中,与代谢综合征的几个独立组分存在显著关联:中心性肥胖(指数关系,P<0.001)、甘油三酯升高(负线性关系,P = 0.018)、高密度脂蛋白胆固醇降低(U型关系,P = 0.086)、血压升高(负线性关系,P = 0.036)以及糖耐量受损(负线性关系,P = 0.036)。在女性中,与中心性肥胖(正线性关系,P<0.001)和血压升高(负线性关系,P = 0.003)存在显著关联,但与其他组分无关联。将这些组分合并为代谢综合征时,在男性中发现呈指数关系(P = 0.017),即仅高出生体重患者的风险增加。在女性中,根本不存在关联(P = 0.959)。
低出生体重与年轻成年人的代谢综合征无关。然而,发现出生体重与该综合征的独立组分之间存在多种关联,但这些关联部分方向不同。