Division of Urology, Duke Prostate Center, Department of Surgery, Duke University Medical Center, Durham, NC, USA.
Cancer Causes Control. 2013 May;24(5):1045-52. doi: 10.1007/s10552-013-0182-4. Epub 2013 Mar 26.
Epidemiological data are conflicting regarding the association between androgenetic alopecia (AA) and prostate cancer (CaP). We examined the relationship between these two conditions.
We performed a case-control study at a Veterans Affairs Hospital among 708 men: 312 healthy controls, 167 men with CaP, and 229 men without CaP on prostate biopsy. Participants were asked to self-describe hair patterns at ages 30 and 40 and at study enrollment. We tested the association between hair pattern (overall, vertex, or frontal) and CaP status using logistic regression analysis adjusting for multiple clinical features. Disease grade was similarly examined as a secondary outcome.
Relative to healthy controls, younger age of AA onset was significantly associated with increased CaP risk (p = 0.008). Similar patterns were noted for frontal (p = 0.005) and not vertex balding (p = 0.22). When compared with biopsy-negative men, a similar pattern was seen with younger age of AA onset having higher risk of CaP, though this was not significant (p = 0.07). A suggestion for younger age of AA onset for frontal (p = 0.07) being associated with CaP versus biopsy-negative men was also observed. Overall balding (yes/no) was associated with greater than twofold increase in high-grade disease (p = 0.02).
Men reporting earlier AA onset were at increased CaP risk and suggestively had more aggressive disease. Contrary to other studies, frontal balding was the predominant pattern associated with elevated CaP risk. Further study is required to confirm these findings in a larger sample and to better understand the role of AA, androgens, and CaP biology.
雄激素性脱发(AA)与前列腺癌(CaP)之间的关联,流行病学数据存在冲突。我们研究了这两种情况之间的关系。
我们在一家退伍军人事务医院进行了一项病例对照研究,共有 708 名男性参与:312 名健康对照者、167 名 CaP 患者和 229 名前列腺活检无 CaP 患者。参与者被要求在 30 岁和 40 岁以及研究入组时自我描述头发模式。我们使用逻辑回归分析测试了头发模式(整体、头顶或额部)与 CaP 状态之间的关联,调整了多种临床特征。疾病分级也作为次要结果进行了同样的检查。
与健康对照组相比,AA 发病年龄较小与 CaP 风险增加显著相关(p = 0.008)。额部(p = 0.005)而非头顶秃发(p = 0.22)也存在类似模式。与活检阴性男性相比,AA 发病年龄较小与 CaP 风险较高具有相似模式,但无统计学意义(p = 0.07)。对于 AA 发病年龄较小与活检阴性男性相比,额部(p = 0.07)与 CaP 相关也有提示作用。整体秃发(是/否)与高级别疾病的两倍以上增加相关(p = 0.02)。
报告 AA 发病年龄较早的男性患 CaP 的风险增加,且提示疾病更具侵袭性。与其他研究相反,额部秃发是与 CaP 风险升高相关的主要模式。需要进一步的研究在更大的样本中证实这些发现,并更好地了解 AA、雄激素和 CaP 生物学的作用。