Rosenberg C R, Shore R E, Pasternack B S
IPRO, Lake Success, NY 11042, USA.
J Community Health. 1995 Aug;20(4):335-43. doi: 10.1007/BF02283058.
A case-control analysis was conducted to determine the relationship between height and mortality among patients enrolled in the already completed Beta Blocker Heart Attack Trial (BHAT). In a basic model including height (continuous) and relevant covariates the relative risk (RR) per 4-inch reduction in height (approximately 1 standard deviation) was 1.18 (95% confidence interval, 0.92 to 1.51). When sex was considered, the effect of short stature on mortality was found to be restricted to male subjects. The male RR per 4-inch reduction in height was 1.26 (0.96 to 1.63) whereas for women it was 0.89 (0.49 to 1.59). In males not randomized to propranolol (untreated) the effect was further modified with a RR per 4-inch reduction in height of 1.41 (1.00 to 1.99). It is hypothesized that short stature could be a marker for factors operating as far back as childhood that predispose males to mortality from coronary heart disease in later life.
进行了一项病例对照分析,以确定已完成的β受体阻滞剂心肌梗死试验(BHAT)中患者的身高与死亡率之间的关系。在一个包含身高(连续变量)和相关协变量的基本模型中,身高每降低4英寸(约1个标准差)的相对风险(RR)为1.18(95%置信区间为0.92至1.51)。当考虑性别时,发现身材矮小对死亡率的影响仅限于男性受试者。身高每降低4英寸,男性的RR为1.26(0.96至1.63),而女性为0.89(0.49至1.59)。在未随机分配到普萘洛尔的男性(未治疗)中,身高每降低4英寸的RR为1.41(1.00至1.99),这进一步改变了上述影响。据推测,身材矮小可能是早在儿童时期就起作用的因素的一个标志,这些因素使男性在晚年易患冠心病死亡。