Travison Thomas G, Shackelton Rebecca, Araujo Andre B, Hall Susan A, Williams Rachel E, Clark Richard V, O'Donnell Amy B, McKinlay John B
New England Research Institutes, Watertown, Massachusetts 02474, USA.
J Am Geriatr Soc. 2008 May;56(5):831-9. doi: 10.1111/j.1532-5415.2008.01679.x.
To describe the onset, progression, and remission of symptomatic androgen deficiency (SAD) using longitudinal data from the Massachusetts Male Aging Study (MMAS).
A prospective, population-based study of men living in Boston, Massachusetts. Data were collected in three waves: T1 (1987/89), T2 (1995/97), T3 (2002/04). Onset, progression, and remission were defined in terms of transitions in SAD status from one wave to the next.
In-person, in-home interviews.
Seven hundred sixty-six community-dwelling men aged 40 to 70 at baseline (T1) contributed data from T1 to T2 and 391 from T2 to T3.
SAD was defined in terms of serum total and free testosterone (T) levels and symptoms associated with low circulating androgens. Total T and sex hormone-binding globulin (SHBG) were measured using radioimmunoassay. Free T was calculated from total T and SHBG measurements.
At T2 or T3, the likelihood of SAD was markedly greater for subjects who had exhibited SAD at the previous wave (odds ratio=3.8, 95% confidence interval=1.9-7.4), overall 55% of subjects who exhibited SAD experienced remission by the next study wave. The probability of SAD was greater with older age and greater body mass index. Multivariate models demonstrated that the likelihood of remission was at least 50% for most subpopulations.
Over approximately 15 years of follow-up, SAD did not represent a stable health state. The likelihood of SAD would remit exceeded the likelihood that it would not, particularly among younger and leaner men.
利用马萨诸塞男性衰老研究(MMAS)的纵向数据,描述症状性雄激素缺乏(SAD)的发病、进展和缓解情况。
对居住在马萨诸塞州波士顿的男性进行的一项基于人群的前瞻性研究。分三个阶段收集数据:T1(1987/89年)、T2(1995/97年)、T3(2002/04年)。根据SAD状态从一个阶段到下一个阶段的转变来定义发病、进展和缓解。
面对面的家庭访谈。
基线时(T1)年龄在40至70岁的766名社区居住男性提供了从T1到T2的数据,391名男性提供了从T2到T3的数据。
根据血清总睾酮和游离睾酮(T)水平以及与低循环雄激素相关的症状来定义SAD。使用放射免疫分析法测量总T和性激素结合球蛋白(SHBG)。根据总T和SHBG测量值计算游离T。
在T2或T3时,前一阶段出现SAD的受试者出现SAD的可能性明显更高(优势比=3.8,95%置信区间=1.9 - 7.4),总体而言,出现SAD的受试者中有55%在下一研究阶段病情缓解。年龄越大、体重指数越高,出现SAD的概率越大。多变量模型表明,大多数亚组病情缓解的可能性至少为50%。
在大约15年的随访中,SAD并非一种稳定的健康状态。SAD病情缓解的可能性超过不缓解的可能性,在年轻和较瘦的男性中尤其如此。