Severi G, Sinclair R, Hopper J L, English D R, McCredie M R E, Boyle P, Giles G G
Division of Epidemiology and Biostatistics, European Institute of Oncology, Milan, Italy.
Br J Dermatol. 2003 Dec;149(6):1207-13. doi: 10.1111/j.1365-2133.2003.05565.x.
The epidemiology of androgenetic alopecia (AGA) is not fully understood. Although a strong genetic basis has long been identified, little is known of its non-genetic causes.
To estimate the prevalence of and to determine risk factors for AGA in men aged 40-69 years in Australia.
Men (n = 1390) were recruited at random from the electoral rolls to serve as controls in a population-based case-control study of prostate cancer. All were interviewed in person and direct observations of AGA were made. Men were grouped into the following categories; no AGA, frontal AGA, vertex AGA and full AGA (frontal and vertex AGA). Epidemiological data collected from these men were used for an analysis of risk factors for each AGA category using unconditional logistic regression with AGA category as the response variable adjusting for age, education and country of birth.
The prevalence of vertex and full AGA increased with age from 31% (age 40-55 years) to 53% (age 65-69 years). Conversely, the proportion of men with only frontal AGA was very similar across all age groups (31-33%). No associations were found between pubertal growth spurt or acne, reports of adult body size at time of interview, urinary symptom score, marital status, or current smoking status or duration of smoking and the risk of any form of AGA. The consumption of alcohol was associated with a significant increase in risk of frontal and vertex AGA but not full AGA. Men with vertex AGA had fewer female sexual partners but average ejaculatory frequency did not differ between men in different AGA categories. Reported weight and lean body mass at reaching maturity at about 21 years of age were negatively associated with vertex balding (P for trend < 0.05) but not with frontal AGA or full AGA.
Evidence for environmental influences on AGA remains very slight. Our study failed to confirm previously reported or hypothesized associations with smoking and benign prostatic hypertrophy. The associations that we found with alcohol consumption and with lean body mass at age 21 years would be worthy of further research if they were able to be replicated in other studies.
雄激素性脱发(AGA)的流行病学尚未完全明确。尽管长期以来已确定其有很强的遗传基础,但对其非遗传病因却知之甚少。
估计澳大利亚40 - 69岁男性AGA的患病率并确定其危险因素。
从选民名单中随机招募男性(n = 1390),作为基于人群的前列腺癌病例对照研究的对照。所有参与者均接受了面对面访谈,并对AGA进行了直接观察。男性被分为以下几类:无AGA、额部AGA、顶部AGA和全秃(额部和顶部AGA)。从这些男性收集的流行病学数据用于分析每个AGA类别的危险因素,使用无条件逻辑回归,以AGA类别作为应变量,并对年龄、教育程度和出生国家进行调整。
顶部和全秃的患病率随年龄增长而增加,从31%(40 - 55岁)增至53%(65 - 69岁)。相反,仅患有额部AGA的男性比例在所有年龄组中非常相似(31 - 33%)。未发现青春期生长突增或痤疮、访谈时报告的成年体型、泌尿系统症状评分、婚姻状况、当前吸烟状况或吸烟持续时间与任何形式AGA的风险之间存在关联。饮酒与额部和顶部AGA的风险显著增加相关,但与全秃无关。患有顶部AGA的男性女性性伴侣较少,但不同AGA类别的男性平均射精频率无差异。报告的约21岁达到成熟时的体重和瘦体重与顶部秃发呈负相关(趋势P < 0.05),但与额部AGA或全秃无关。
环境对AGA影响的证据仍然非常少。我们的研究未能证实先前报道或假设的与吸烟和良性前列腺增生的关联。如果我们发现的饮酒与21岁时瘦体重的关联能够在其他研究中得到重复,那么将值得进一步研究。