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Purpose: We aimed to investigate the prevalence and the diagnostic criteria of hypoprolactinemia in patients with panhypopituitarism and the effects of hypoprolactinemia on depression and sexual functions.
Materials And Methods: Forty-eight patients with panhypopituitarism and 20 healthy volunteers were included. Basal hormone levels were measured and a TRH stimulation test was performed. For the evaluation of sexual functions, questionnaries of Female Sexual Functional Index (FSFI) for females and International Erectile Functional Index for males were performed to the subjects. Depressive symptoms were evaluated by Beck Depression Envontory score (BDI-II).
Results: The peak PRL response to TRH stimulation test at 5th percentile in the control group was 18.6 ng/ml in males and 41.6 ng/ml in females and accepted as the cut-offs for sufficient response of PRL. Prolactin was insufficient in 42(87.5%) patients. A basal PRL level of ≤ 5.7 ng/ml in males and 7.11 ng/ml in females was 100% specific in predicting an inadequate response to TRH stimulation test with 80% and 70% sensitivity respectively. A basal PRL level of ≥ 8.5 ng/dl in males was 100% specific and 76% sensitive, and in females a level of ≥ 15.2 ng/dl was 96% specific and 66% sensitive in predicting an adequate response to TRH. PRL deficient patients with panhypopituitarism had higher depression scores compared to the controls, lower sexual function scores in males.
Conclusion: PRL deficiency is prevalent among individuals with panhypopituitarism, with the potential to result in elevated depression scores in both sexes and impaired sexual functions in males. A basal PRL level seems to be sufficient for the diagnosis of hypoprolactinemia in routine clinical practice.
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http://dx.doi.org/10.1007/s11102-024-01393-0 | DOI Listing |
J Pediatr Endocrinol Metab
September 2025
Division of Endocrinology, Diabetes and Metabolism, ENDO-ERN Center for Rare Paediatric Endocrine Diseases, First Department of Pediatrics, Medical School, 68993 National and Kapodistrian University of Athens, "Aghia Sophia" Children's Hospital, Athens, Greece.
Objectives: The majority of congenital hypopituitarism (CH) cases remain genetically unexplained. The transmembrane receptor Roundabout-1 (), activated through interaction with SLIT-family proteins, plays crucial role in axonal guidance, branching, targeting, and midline axonal crossing. variants have been associated with pituitary stalk interruption syndrome and highly variable pituitary-phenotypes, ranging from isolated growth hormone deficiency (IGHD) to combined pituitary hormone deficiency (CPHD).
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Division of Nephrology, Faculty of Medicine, Tohoku Medical and Pharmaceutical University, Japan.
Hypopituitarism can cause various psychiatric disorders. We herein report the case of a 60-year-old female with hypopituitarism who presented with severe hyponatremia, impaired consciousness, and delusional disorder. Brain imaging revealed a pituitary macrotumor with hemorrhaging, and the laboratory findings suggested panhypopituitarism.
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September 2025
Clinical Genetics unit, Department of Women's and Children's Health, University of Padova, Padova, Italy.
Short stature (SS) is one of the most frequent reasons for referral to paediatric endocrinologists. Linear growth is a multifactorial process, with genetic variation representing the principal determinant of height differences. Between 2018 and 2022, 102 children referred to our clinic for growth failure were identified as having SS of unknown aetiology.
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Dhaka Medical College and Hospital, Secretariat Road, Shahbagh, Dhaka 1000, Bangladesh.
Neurosarcoidosis is a rare and often challenging condition that primarily affects the central nervous system, frequently leading to complex endocrine disorders. This case report presents an uncommon manifestation of neurosarcoidosis in a 30-year-old woman who developed panhypopituitarism, complicated by diabetes insipidus (DI) and subclinical multifocal pneumonitis. The patient had a 1-year history of low-grade intermittent fevers, cognitive decline, unintentional weight loss, and symptoms of DI, including excessive thirst and urination.
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July 2025
Department of Neurosurgery, Chrisitan Doppler Clinic Salzburg, Paracelsus Private Medical University, Salzburg, AUT.
This article presents the first documented case of a 61-year-old patient who underwent radical transnasal transsphenoidal endoscopic resection of a pituitary metastasis from a squamous cell carcinoma (SCC) of the tonsils. Only two other cases of pituitary metastases in SCC have been described in the literature to date. The patient was diagnosed with p16 and human papillomavirus (HPV)-positive tonsillar SCC in June 2022.
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