Research · PMID 35904664

PubMed sourcedAbstract-based analysis

Reviewed by Neal Rouzier, MD, Preventive Medicine · Sep 2026

Obstructive sleep apnea and serum total testosterone: a system review and meta-analysis.

Sleep & breathing = Schlaf & Atmung · June 2023 · Huihui Wang, Jiyuan Lu, Lingdan Xu, Yanduo Yang, Yucheng Meng, et al.

What this study found

The results indicated that OSA is significantly correlated with the decrease in serum testosterone levels in men. Male patients with OSA should be alerted to secondary diseases caused by low testosterone levels.

systematic_review

How RAGMD uses this study

Clinical questions this paper informs

Synthesis lives on the evidence question — this page shows where the study sits in that analysis.

Primary study

Does testosterone therapy worsen obstructive sleep apnea?

Testosterone may worsen sleep apnea in predisposed men. Screening and monitoring for OSA is recommended before and during therapy, especially when symptoms emerge or hematocrit rises.

Open evidence analysis

Supporting literature

Does testosterone replacement increase cardiovascular risk?

Large randomized data (including TRAVERSE) do not show a significant increase in major adverse cardiovascular events with testosterone therapy in hypogonadal men over median follow-up of roughly three years. Older observational studies conflict, and absolute risk depends on baseline cardiovascular disease, formulation, and monitoring.

Open evidence analysis

Supporting literature

Does testosterone therapy increase prostate cancer risk?

Current systematic reviews and trial secondary analyses do not show a convincing increase in prostate cancer incidence among hypogonadal men treated with testosterone, though surveillance remains standard practice.

Open evidence analysis

Supporting literature

Does testosterone therapy increase hematocrit and polycythemia risk?

Testosterone therapy commonly raises hematocrit; polycythemia is a recognized adverse effect requiring dose adjustment, formulation changes, or phlebotomy when thresholds are exceeded.

Open evidence analysis

Supporting literature

Does testosterone therapy suppress fertility in men?

Exogenous testosterone suppresses the hypothalamic-pituitary-gonadal axis and reliably reduces spermatogenesis. Recovery after discontinuation is variable and may be incomplete in some men.

Open evidence analysis

Supporting literature

Does testosterone therapy increase venous thromboembolism risk?

Large observational cohorts suggest a modest increase in venous thromboembolism risk with testosterone therapy, particularly early after initiation. Absolute risk remains low in most populations but warrants attention in predisposed patients.

Open evidence analysis

Supporting literature

Does testosterone therapy reduce cardiovascular events?

TRAVERSE found no significant difference in major adverse cardiovascular events between testosterone and placebo over trial follow-up. Meta-analyses of earlier trials are mixed; testosterone should not be prescribed primarily for cardiovascular protection.

Open evidence analysis

Supporting literature

Does estradiol level affect symptoms and bone health in men on testosterone therapy?

Estradiol in men derives largely from aromatization of testosterone and contributes to bone density and possibly symptom control. Over-suppression with aromatase inhibitors may impair bone health; optimal targets in clinical practice remain debated.

Open evidence analysis

Supporting literature

Do aromatase inhibitors in men increase bone loss risk?

Aromatase inhibitors lower estradiol and can reduce bone mineral density in men. Routine use to suppress estradiol during testosterone therapy is not supported by outcome evidence and may carry skeletal risk.

Open evidence analysis

Supporting literature

How should low testosterone be diagnosed in symptomatic men?

Diagnosis requires consistent symptoms plus repeatedly low morning total testosterone on valid assays, with secondary causes excluded. A single borderline value should prompt repeat testing before initiating therapy.

Open evidence analysis