Reproductive endocrinology

Increased Morbidity in Males Diagnosed With Gynecomastia: A Nationwide Register-based Cohort Study

J Clin Endocrinol MetabPublished Register-based cohort study

Authors' conclusion

The presence of idiopathic gynecomastia is an important first clinical symptom of an underlying disease and a significant predictor of future disease risk. These findings should stimulate more awareness among health care providers to increase identification of gynecomastia and its causes in males.

Study context

Population
Males diagnosed with incident gynecomastia and matched males from the background population1:5 age-/calendar-matched cohort
Participants
23,429 / 16,253 / 117,145
Exposure
Males with gynecomastia vs matched males without gynecomastia
  • Gynecomastian = 23,429
  • Idiopathic gynecomastian = 16,253
  • Without gynecomastian = 117,145reference
Outcome
Disease risk by ICD-10 sections following and before gynecomastia diagnosis
Methodological detailsnationwide, age- and calendar-matched (1:5)
  • Nationwide
  • Age- and calendar-matched (1:5)

Main finding

As reported in the abstract

Risk of future disease (ICD-10 chapters) after idiopathic gynecomastia vs matched males without gynecomastia

Higher risk of future disease across all included disease chapters (HR range)

HR, 1.19-1.89

Endocrine diseases, greatest disease risk

HR, 1.89; 95% CI, 1.76-2.03

Highest subchapter risk: disorders of the endocrine glands

OR, 7.27; 95% CI, 6.19-8.54

Observational data: associations, not effects.

Further findings

Comorbidities before gynecomastia diagnosis (ICD-10 sections)

ORs of comorbidities higher across all included disease sections (OR range)
OR, 1.05-1.51
Except psychiatric disease
OR, 0.72; 95% CI, 0.68-0.78
Musculoskeletal/connective tissue diseases, highest association
OR, 1.51; 95% CI, 1.46-1.57
Circulatory diseases
OR, 1.36; 95% CI, 1.29-1.43

Original publication

Increased Morbidity in Males Diagnosed With Gynecomastia: A Nationwide Register-based Cohort Study. J Clin Endocrinol Metab. Published 31 January 2023. doi:10.1210/clinem/dgad048

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