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Intraindividual variation in levels of serum testosterone and other reproductive and adrenal hormones in men.男性血清睾酮及其他生殖和肾上腺激素水平的个体内变异。
Clin Endocrinol (Oxf). 2007 Dec;67(6):853-62. doi: 10.1111/j.1365-2265.2007.02976.x.
2
Prevalence of symptomatic androgen deficiency in men.男性有症状性雄激素缺乏的患病率。
J Clin Endocrinol Metab. 2007 Nov;92(11):4241-7. doi: 10.1210/jc.2007-1245. Epub 2007 Aug 14.
3
Part of the interindividual variation in serum testosterone levels in healthy men reflects differences in androgen sensitivity and feedback set point: contribution of the androgen receptor polyglutamine tract polymorphism.健康男性血清睾酮水平的个体差异部分反映了雄激素敏感性和反馈设定点的差异:雄激素受体多聚谷氨酰胺序列多态性的作用。
J Clin Endocrinol Metab. 2007 Sep;92(9):3604-10. doi: 10.1210/jc.2007-0117. Epub 2007 Jun 19.
4
Adding to the controversy: pitfalls in the diagnosis of testosterone deficiency syndromes with questionnaires and biochemistry.争议加剧:使用问卷和生物化学方法诊断睾酮缺乏综合征时的陷阱。
Aging Male. 2007 Jun;10(2):57-65. doi: 10.1080/13685530701342686.
5
Testosterone, sex hormone-binding globulin, and frailty in older men.老年男性的睾酮、性激素结合球蛋白与衰弱
J Am Geriatr Soc. 2007 Apr;55(4):548-55. doi: 10.1111/j.1532-5415.2007.01121.x.
6
The relative contributions of aging, health, and lifestyle factors to serum testosterone decline in men.衰老、健康和生活方式因素对男性血清睾酮水平下降的相对影响。
J Clin Endocrinol Metab. 2007 Feb;92(2):549-55. doi: 10.1210/jc.2006-1859. Epub 2006 Dec 5.
7
A population-level decline in serum testosterone levels in American men.美国男性血清睾酮水平出现总体下降。
J Clin Endocrinol Metab. 2007 Jan;92(1):196-202. doi: 10.1210/jc.2006-1375. Epub 2006 Oct 24.
8
Making a diagnosis of androgen deficiency in adult men: what to do until all the facts are in?成年男性雄激素缺乏的诊断:在掌握全部事实之前该怎么做?
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Association of specific symptoms and metabolic risks with serum testosterone in older men.老年男性特定症状和代谢风险与血清睾酮的关联
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The effect of changes in adiposity on testosterone levels in older men: longitudinal results from the Massachusetts Male Aging Study.肥胖变化对老年男性睾酮水平的影响:来自马萨诸塞州男性衰老研究的纵向结果。
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男性有症状雄激素缺乏的自然病史:发病、进展及自发缓解

The natural history of symptomatic androgen deficiency in men: onset, progression, and spontaneous remission.

作者信息

Travison Thomas G, Shackelton Rebecca, Araujo Andre B, Hall Susan A, Williams Rachel E, Clark Richard V, O'Donnell Amy B, McKinlay John B

机构信息

New England Research Institutes, Watertown, Massachusetts 02474, USA.

出版信息

J Am Geriatr Soc. 2008 May;56(5):831-9. doi: 10.1111/j.1532-5415.2008.01679.x.

DOI:10.1111/j.1532-5415.2008.01679.x
PMID:18454749
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5556701/
Abstract

OBJECTIVES

To describe the onset, progression, and remission of symptomatic androgen deficiency (SAD) using longitudinal data from the Massachusetts Male Aging Study (MMAS).

DESIGN

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.

SETTING

In-person, in-home interviews.

PARTICIPANTS

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.

MEASUREMENTS

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.

RESULTS

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.

CONCLUSION

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.

摘要

目的

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。

设计

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。

地点

面对面的家庭访谈。

参与者

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。

测量

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。

结果

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%。

结论

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。