AI Article Synopsis

  • Autonomous cortisol secretion (ACS) from adrenal adenomas can lead to higher risks of comorbidities and mortality, and the dexamethasone suppression test (DST) is essential for its diagnosis.
  • A study involving 24,259 adults found only about 7% completed a DST, with factors such as male sex and high comorbidity index linked to lower completion rates.
  • To enhance detection and management of adrenal adenomas, clinical policies must be developed to encourage more patients to complete the DST.

Article Abstract

Autonomous cortisol secretion (ACS) from an adrenal adenoma can increase the risk for comorbidities and mortality. The dexamethasone suppression test (DST) is the standard method to diagnose ACS. A multi-site, retrospective cohort of adults with diagnosed adrenal tumors was used to understand patient characteristics associated with DST completion and ACS. Time to DST completion was defined using the lab value and result date; follow-up time was from the adrenal adenoma diagnosis to the time of completion or censoring. ACS was defined by a DST > 1.8 µg/dL (50 nmol/L). The Cox proportional hazards regression model assessed associations between DST completion and patient characteristics. In patients completing a DST, a logistic regression model evaluated relationships between elevated ACS and covariates. We included 24,259 adults, with a mean age of 63.1 years, 48.1% obese, and 28.7% with a Charlson comorbidity index ≥ 4. Approximately 7% (n = 1768) completed a DST with a completion rate of 2.36 (95% CI 2.35, 2.37) per 100 person-years. Fully adjusted models reported that male sex and an increased Charlson comorbidity index were associated with a lower likelihood of DST completion. Current or former smoking status and an increased Charlson comorbidity index had higher odds of a DST > 1.8 μg/dL. In conclusion, clinical policies are needed to improve DST completion and the management of adrenal adenomas.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10740617PMC
http://dx.doi.org/10.3390/biomedicines11123167DOI Listing

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