Benign prostatic hyperplasia, metabolic syndrome and androgenic alopecia: Is there a possible relationship?

• Published in: Arab Journal of Urology Vol. 14; no. 2; pp. 157 - 162
• Main Authors: Agamia, Naglaa F., Abou Youssif, Tamer, El-Hadidy, Abeer, El-Abd, Amr
• Format: Journal Article
• Language: English
• Published: United States Elsevier B.V 01.06.2016; Taylor & Francis; Elsevier
• Subjects: AGA; Androgenetic alopecia; Benign prostatic hyperplasia; BMI; body mass index; C-reactive protein; cardiovascular disease; Cardiovascular risk; CRP; CVD; DHT; dihydrotestosterone; erythrocyte sedimentation rate; ESR; fasting blood sugar; FBS; glycosylated haemoglobin; HbA1c; HDL; high-density lipoprotein; Metabolic syndrome; Prostatic Disorders Original article; CRP; ESR; Metabolic syndrome; CVD; DHT; HDL; FBS; Cardiovascular risk; Benign prostatic hyperplasia; AGA; HbA1c; Androgenetic alopecia; BMI; FBS, fasting blood sugar; DHT, dihydrotestosterone; CVD, cardiovascular disease; ESR, erythrocyte sedimentation rate; BMI, body mass index; HbA1c, glycosylated haemoglobin; AGA, androgenetic alopecia; CRP, C-reactive protein; HDL, high-density lipoprotein
• ISSN: 2090-598X; 2090-5998; 2090-598X; 2090-5998
• DOI: 10.1016/j.aju.2016.01.003

To evaluate the incidence of benign prostatic hyperplasia (BPH) and metabolic syndrome in patients with androgenetic alopecia (AGA) in comparison with those with no AGA, as several previous studies have reported inconsistent results of an association between metabolic syndrome and BPH with AGA. This cross-sectional study included 400 participants, divided into 300 patients diagnosed with AGA, with different grades according to Norwood–Hamilton classification, and 100 control subjects with no AGA. Criteria for diagnosis of metabolic syndrome according to Adult Treatment Panel-III criteria (waist circumference, blood pressure, fasting blood sugar, high-density lipoprotein and triglycerides), as well as criteria for diagnosis of BPH (prostatic volume, urine flow, and prostate-specific antigen) were assessed in all patients and compared with the control subjects. There were significant differences between the AGA and no-AGA groups for the following variables: waist circumference, body mass index, fibrinogen level, fasting blood sugar, cholesterol, C-reactive protein, erythrocyte sedimentation rate, and glycosylated haemoglobin. There was a significant difference in number of patients with AGA manifesting criteria of metabolic syndrome (51% vs 28%), as well as BPH diagnostic criteria (36% vs 6.8%) compared with the control subjects. Both BPH and metabolic syndrome were shown to be significant independent variables associated with AGA. Dermatologists, urologists, and primary care physicians should monitor patients with early onset AGA for the development of urinary symptoms, to permit an earlier diagnosis of BPH; and for metabolic syndrome symptoms, to permit early diagnosis of cardiovascular risk factors.