Pituitary & hypothalamus

Primary Autoimmune Hypophysitis: Treatment and Predictors of Response to Glucocorticoid in a Single Center in China

Endocr PractPublished Retrospective cohort study

Authors' conclusion

GC therapy was effective in achieving both endocrine and radiological remission in patients with PAH. Younger patients were more prone to endocrine response to GC therapy, whereas growth hormone deficiency emerged as an independent unfavorable factor for radiological response to GC treatment.

Study context

Population
Patients diagnosed with primary autoimmune hypophysitis (PAH) at a single center in China, December 2009 to October 2022
Participants
77 patients
Exposure
Glucocorticoid (GC) therapy vs no GC therapy
Outcome
Radiological recovery/improvement
Methodological detailssingle-centre
  • Single-centre

Main finding

As reported in the abstract

P = 0.025

Observational data: associations, not effects.

Further findings

Predictor of endocrine response to GC: age at diagnosis

OR (CI)P value
Age at diagnosisYounger age an independent favorable factor · logistic regression0.897 (0.808–0.995)P = 0.040

Predictor of radiological response to GC: presence of growth hormone deficiency

OR (CI)P value
Presence of growth hormone deficiencyIndependent unfavorable factor · logistic regression0.094 (0.015–0.580)P = 0.011

Clinical features of PAH

Headache (most common symptom)
64.9%
Hypogonadotropic hypogonadism (most common anterior pituitary deficiency)
58.9%
Secondary hypocortisolism
57.1%
Secondary hypothyroidism
52.6%
Vasopressin deficiency
61.8%

Original publication

Primary Autoimmune Hypophysitis: Treatment and Predictors of Response to Glucocorticoid in a Single Center in China. Endocr Pract. Published 30 December 2025. doi:10.1016/j.eprac.2025.12.015

Composed by AI from the published abstract and checked against it. How Briefs are made →

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