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Dilated cardiomyopathy in patients with hypoparathyroidism: A narrative review
Maryam Abdolmaleki1, Laya Ohadi1, Saba Maleki2
1Shahid Beheshti University of Medical Sciences Tehran Iran.
Insights
Hypoparathyroidism can cause dilated cardiomyopathy (DCM), but timely calcium and vitamin D supplementation can reverse cardiac dysfunction. Patient adherence to treatment is key for managing this endocrine-related heart condition.
Area of Science:
- Endocrinology
- Cardiology
Background:
- Hypoparathyroidism is a rare endocrine disorder marked by low calcium, high phosphorus, and insufficient parathyroid hormone.
- This condition can lead to dilated cardiomyopathy (DCM), characterized by enlarged heart ventricles and impaired function.
Purpose of the Study:
- To explore the link between hypoparathyroidism and DCM.
- To investigate calcium's impact on cardiac function.
- To assess the potential for DCM reversal with calcium supplementation.
Main Methods:
- A comprehensive literature search was performed using PubMed and Google Scholar.
- Included case reports of DCM in hypoparathyroidism patients.
- Analyzed cases for cardiac manifestations, diagnostics, and management.
Main Results:
- DCM in hypoparathyroidism presents with heart failure symptoms, reduced ejection fraction, and impaired left ventricular function.
- Laboratory findings include low serum calcium and high phosphate levels.
- Prompt treatment with calcium and vitamin D improved cardiac function.
Conclusions:
- Hypoparathyroidism-induced DCM is reversible with timely calcium and vitamin D supplementation.
- Patient compliance and regular monitoring are crucial for preventing cardiac complications.
- Routine follow-up of DCM in endocrine disorder patients is recommended.
Background:
Hypoparathyroidism is a rare endocrine disorder characterized by low blood calcium levels, elevated phosphorus levels, and insufficient parathyroid hormone production. It can lead to dilated cardiomyopathy (DCM), a cardiac condition characterized by enlarged ventricles and reduced heart function. This review aims to explore the relationship between hypoparathyroidism and DCM, the impact of calcium on cardiac function, and the potential for DCM reversal with calcium supplementation.
Methods:
A comprehensive literature search was conducted using PubMed, Google Scholar, and relevant keywords and Mesh terms. Case reports evaluating dilated cardiomyopathy in patients with Hypoparathyroidism were included in the study. Additionally, references cited in each study were carefully examined to identify relevant reports. The cases included in the review were analyzed, and common cardiac manifestations, diagnostic approaches, and management were identified.
Results:
DCM in hypoparathyroidism presents with symptoms of heart failure, reduced ejection fraction, and impaired left ventricular function. Laboratory tests show low serum calcium levels and elevated phosphate levels. Prompt diagnosis and treatment with calcium and vitamin D supplementation can lead to improvements in cardiac function.
Conclusion:
Hypoparathyroidism-induced DCM is reversible with timely calcium and vitamin D supplementation. Patient compliance with prescribed medications and supplements is crucial to prevent and manage cardiac complications. Regular follow-up check-ups and monitoring of calcium levels can aid in early detection and improve patient outcomes. Educating patients about the importance of treatment adherence can significantly reduce the risk of developing DCM and other cardiac symptoms associated with hypoparathyroidism. Routine follow-up of DCM among patients with endocrine disorders is recommended.
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