Tchernof André, Labrie Fernand
Molecular Endocrinology and Oncology Research Center, Laval University Hospital Research Center (CHUL Research Center) and Laval University, Quebec G1V 4G2, Canada.
Eur J Endocrinol. 2004 Jul;151(1):1-14. doi: 10.1530/eje.0.1510001.
The age-related decline in serum dehydroepiandrosterone (DHEA) and its sulfated ester (DHEA-S) has suggested that a relative deficiency of these steroids may be causally related to the development of chronic diseases generally associated with aging, including insulin resistance, obesity, cardiovascular disease, cancer, reductions of the immune defense, depression and a general deterioration in the sensation of well-being. The numerous studies which have focused on the link between DHEA and cardiovascular disease have generally been inconsistent, generating much debate and controversy on this issue. The present article is an analysis of studies on the relationship between endogenous DHEA or DHEA-S, obesity and cardiovascular disease risk, as well as DHEA treatment studies. Elevated plasma levels of free DHEA are associated with reduced obesity in both men and women, and with smaller abdominal body fat accumulations in men. However, contradictory results have been reported regarding the relationships between the sulfate ester DHEA-S and adiposity. Age differences in the populations studied may have been a confounding factor in these associations. On the other hand, DHEA-S level is not a predictor of cardiovascular disease endpoints in women, and appears to be a relatively weak one in men. DHEA intervention studies suggest that the effects of DHEA on serum lipids are, at best, modest or non-significant. The uncertainty as to whether endogenous and exogenous DHEA should be considered cardioprotective is related to discrepancies in the literature on this topic. Several studies may have been plagued by methodological problems such as low power, unreliable analytical methods, confounding factors or other differences in the populations studied. As a consequence, the original reports demonstrating dramatic effects of either endogenous or exogenous DHEA on cardiovascular disease risk have never been replicated. We propose that the effects of DHEA on cardiovascular disease risk (either favorable or unfavorable) should be considered to be much more modest than previously believed.
血清脱氢表雄酮(DHEA)及其硫酸酯(DHEA-S)随年龄增长而下降,这表明这些类固醇的相对缺乏可能与通常与衰老相关的慢性疾病的发生存在因果关系,这些慢性病包括胰岛素抵抗、肥胖、心血管疾病、癌症、免疫防御功能减退、抑郁症以及总体幸福感的普遍下降。众多关注DHEA与心血管疾病之间联系的研究结果通常并不一致,在这个问题上引发了诸多争论和争议。本文对有关内源性DHEA或DHEA-S、肥胖与心血管疾病风险之间关系的研究以及DHEA治疗研究进行了分析。游离DHEA血浆水平升高与男性和女性肥胖程度降低相关,且与男性腹部体脂堆积减少有关。然而,关于硫酸酯DHEA-S与肥胖之间的关系,已有相互矛盾的报道。所研究人群的年龄差异可能是这些关联中的一个混杂因素。另一方面,DHEA-S水平并非女性心血管疾病终点的预测指标,在男性中似乎也是一个相对较弱的指标。DHEA干预研究表明,DHEA对血脂的影响充其量只是适度的或不显著的。内源性和外源性DHEA是否应被视为具有心脏保护作用尚不确定,这与该主题文献中的差异有关。一些研究可能受到方法学问题的困扰,如检验效能低、分析方法不可靠、混杂因素或所研究人群的其他差异。因此,那些表明内源性或外源性DHEA对心血管疾病风险有显著影响的原始报告从未被重复验证过。我们认为,DHEA对心血管疾病风险的影响(无论是有利还是不利)应被视为比之前认为的要小得多。