Key result
Ischemic sudden cardiac death linked to pituitary cell enlargement in younger victims but atrophy in older.
Why the study?
Morphometric changes in the adenohypophysis during sudden cardiac death and their age-related characteristics were not well described.
Observational (n=75)
No
Morphometric analysis of the pituitary gland during sudden cardiac death reveals that underlying ischemic heart disease drives hyperproductive cellular enlargement in younger individuals but accelerates atrophic and sclerotic involution in older patients.
Answers are grounded in this paper and cite their sources.
Should not alter SCD risk assessment or management; leaves open age-specific pituitary mechanisms in IHD.
The study describes morphometric changes in the adenohypophysis during sudden cardiac death. The study investigated the morphometric parameters of pituitary gland tissues obtained from 75 individuals who died of sudden cardiac death, categorized according to the WHO age classification into cohorts of 18–44, 45–59, 60–74, and 75–90 years and older. The specimens were examined at the Andijan branch of the Republican Scientific and Practical Center for Forensic Medical Examination during the period of 2015–2024. In acute cardiac death associated with ischemic heart disease (IHD), age-specific features revealed that in the 18–44 and 45–59 age groups, the diameters of acidophilic cells, thyrotroph cells, corticotroph cells, and gonadotroph cells significantly increased; these indicators explained the enhancement of metabolic processes and morphofunctional activity in them. In the 60–74 and 75–90 age groups, a statistically significant decrease in the diameters of acidophilic cells, thyrotroph cells, corticotroph cells, and gonadotroph cells was observed, which manifested a decline in cellular metabolic processes. A decrease in the area occupied by the adenohypophyseal parenchyma accompanied by an increase in the stromal area occurred in parallel with advancing age, demonstrating a decline in the gland's morphofunctional activity. These changes were explained by the fact that age-related atrophic and sclerotic alterations of the pituitary gland in these individuals were accelerated against the background of IHD, and atrophic changes accelerated the aging processes.
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Khojiakbar et al. (2026) conducted an observational in Sudden Cardiac Death associated with Ischemic Heart Disease (n=75). Ischemic heart disease resulting in sudden cardiac death vs. Age-matched controls without ischemic heart disease was evaluated on Diameter of acidophilic cells in the 18-44 age cohort (μm) (p=0.01). Sudden cardiac death associated with ischemic heart disease caused a significant increase in pituitary cell diameters in younger individuals (18-59 years) but accelerated cellular atrophy and sclerosis in older individuals (60-90 years).
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