TY - JOUR
T1 - Androgen therapy in midlife and older women
T2 - a position statement of the Latin American Association of Gynecological Endocrinology (ALEG)
AU - Pilnik, Susana
AU - Belardo, Alejandra
AU - Marchesan, Lucas Bandeira
AU - Camero-Lascano, Adriana
AU - Acuña-San Martín, Margot
AU - Elizalde-Cremonte, Alejandra
AU - Ojeda, Eliana
AU - Manzur, Alejandro
AU - Chedraui, Peter
N1 - Publisher Copyright:
© 2025 International Menopause Society.
PY - 2025
Y1 - 2025
N2 - Objective: Androgens have been prescribed to alleviate symptoms in midlife women, but evidence regarding benefits and risks remains limited, with no clearly established indications for Testosterone therapy. In many Latin American countries, Testosterone is prescribed without specific guidelines, making it difficult to identify patients who might benefit. This position statement aims to summarize evidence and provide a Latin American perspective on androgen therapy in midlife and older women. Method: Data were collected from Cochrane reviews, placebo-controlled studies, meta-analyses, international guidelines, consensus statements, and government regulations published between 2000 and the present. Analyses focused on efficacy, safety, and clinical recommendations for androgen therapy in midlife and older women. Results: Testosterone therapy for postmenopausal women should be limited to those with hypoactive sexual desire disorder (HSDD) confirmed through a formal biopsychosocial evaluation (Grade A: High). Routine serum measurements of Testosterone or other androgens are not recommended for diagnosis (Grade A: High), but baseline levels should be checked before therapy to exclude elevated concentrations (Grade C: Low). Treatment monitoring should occur within 3–6 weeks, maintaining Testosterone within the premenopausal physiological range (Grade C: Low). Transdermal formulations are preferred. Subcutaneous pellets and compounded “bioidentical” Testosterone are not recommended due to risks of supraphysiological dosing and insufficient evidence (Grade C: Low). Oral dehydroepiandrosterone (DHEA) is not advised systemically (Grade A: High). Vaginal DHEA is approved only for genitourinary syndrome of menopause. Conclusion: Women should receive counseling aligned with current clinical guidelines. Prior to initiating Testosterone therapy, patients must be informed that its use is off-label. Evidence to date does not support systemic DHEA as an effective treatment for sexual symptoms.
AB - Objective: Androgens have been prescribed to alleviate symptoms in midlife women, but evidence regarding benefits and risks remains limited, with no clearly established indications for Testosterone therapy. In many Latin American countries, Testosterone is prescribed without specific guidelines, making it difficult to identify patients who might benefit. This position statement aims to summarize evidence and provide a Latin American perspective on androgen therapy in midlife and older women. Method: Data were collected from Cochrane reviews, placebo-controlled studies, meta-analyses, international guidelines, consensus statements, and government regulations published between 2000 and the present. Analyses focused on efficacy, safety, and clinical recommendations for androgen therapy in midlife and older women. Results: Testosterone therapy for postmenopausal women should be limited to those with hypoactive sexual desire disorder (HSDD) confirmed through a formal biopsychosocial evaluation (Grade A: High). Routine serum measurements of Testosterone or other androgens are not recommended for diagnosis (Grade A: High), but baseline levels should be checked before therapy to exclude elevated concentrations (Grade C: Low). Treatment monitoring should occur within 3–6 weeks, maintaining Testosterone within the premenopausal physiological range (Grade C: Low). Transdermal formulations are preferred. Subcutaneous pellets and compounded “bioidentical” Testosterone are not recommended due to risks of supraphysiological dosing and insufficient evidence (Grade C: Low). Oral dehydroepiandrosterone (DHEA) is not advised systemically (Grade A: High). Vaginal DHEA is approved only for genitourinary syndrome of menopause. Conclusion: Women should receive counseling aligned with current clinical guidelines. Prior to initiating Testosterone therapy, patients must be informed that its use is off-label. Evidence to date does not support systemic DHEA as an effective treatment for sexual symptoms.
KW - Testosterone
KW - androgens
KW - dehydroepiandrosterone
KW - hypoactive sexual desire disorder
KW - treatment
UR - https://www.scopus.com/pages/publications/105015390928
U2 - 10.1080/13697137.2025.2548805
DO - 10.1080/13697137.2025.2548805
M3 - Artículo de revisión
AN - SCOPUS:105015390928
SN - 1369-7137
VL - 28
SP - 529
EP - 536
JO - Climacteric
JF - Climacteric
IS - 5
ER -