UNRAVELING THE LINK BETWEEN SHEEHAN’S SYNDROME AND LIVER DYSFUNCTION
Main Article Content
Keywords
Sheehan’s Syndrome, Hypopituitarism, Postpartum Hemorrhage, Endocrine dysfunction, Liver dysfunction, Non-alcoholic steatohepatitis .
Abstract
Background:
Sheehan’s Syndrome (SS) is a rare but serious cause of hypopituitarism in postpartum women, often resulting from ischemic necrosis of the pituitary gland due to severe postpartum hemorrhage. This study aims to evaluate the clinical, biochemical, and hormonal profiles of SS patients and compare them with age- and Body Mass Index (BMI)-matched healthy controls.
Materials and Methods:
A case-control study was conducted with 30 patients diagnosed with Sheehan’s Syndrome and 30 age- and BMI-matched healthy controls. Patients were recruited from the endocrine clinic of Government Medical College, Srinagar, and the diagnosis was established based on clinical history, MRI findings (empty sella), and hormonal deficiencies. Fasting morning blood samples were analyzed for glucose, Follicle-Stimulating Hormone (FSH), Luteinizing Hormone (LH), Thyroid-Stimulating Hormone (TSH), Growth Hormone (GH), Prolactin (PRL), Cortisol, and Free T4 using Immunoradiometric Assay (IRMA). Routine hematological, kidney, and liver function tests were performed. Data were analyzed using SPSS Version 20.0, and a p-value <0.05 was considered statistically significant.
Results:
The mean age of patients and controls was 47.7 ± 4.47 years and 47.3 ± 4.34 years, respectively. The average diagnostic delay was 11.35 ± 4.47 years. BMI analysis revealed that 53.3% of SS patients had normal BMI, 33.3% were overweight, and 13.3% were obese. Hormonal deficiencies were highly prevalent, with GH deficiency in 89.9% of patients, Cortisol deficiency in 84%, PRL deficiency in 72%, LH deficiency in 60%, and FSH deficiency in 40%. Liver function abnormalities were significantly more frequent in SS patients, with 73.3% showing elevated ALT (>40 IU/L, p = 0.009) and 76.7% having elevated ALP (>150 IU/L, p < 0.001). However, bilirubin, AST, and albumin levels did not differ significantly between the two groups.
Conclusion:
Sheehan’s Syndrome is associated with profound pituitary hormone deficiencies and notable liver function abnormalities. In this study observed findings explores a significant association between Sheehan’s Syndrome and metabolic alterations, particularly liver dysfunction, suggesting a potential link between hypopituitarism and non-alcoholic steatohepatitis.
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