Transplantation of heterozygous familial hypercholesterolemia living donor liver resulting in early myocardial infarction: a possible dangerous link

Submitted: January 9, 2024
Accepted: January 14, 2024
Published: January 16, 2024
Abstract Views: 435
PDF_EARLY VIEW: 254
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Authors

Living donor liver transplantation (LDLT) is a lifesaving procedure that is often curative for several liver diseases. Familial hypercholesterolemia (FH) is a metabolic disease that results from an autosomal dominant mutation in the low-density lipoprotein receptor; yet, young patients with FH can live years without detection. Herein, we report a case of a patient who developed early myocardial infarction (MI) after having a transplant from a donor with undetected heterozygous FH. This was a 67-year-old female with non-alcoholic steatohepatitis-related liver cirrhosis, free from coronary artery disease, who underwent LDLT from her daughter, a 45-year-old female with no past medical history. One year post-transplant, she presented with an acute MI with a large atherosclerotic burden. Genetic analysis confirmed heterozygous FH in the donor but not in the recipient. This case emphasizes the importance of incorporating a thorough clinical history and lipid profile into pre-transplant testing for both the recipient and donor, as well as aggressive lipid-lowering therapy post-transplantation to avoid cardiovascular complications.

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Citations

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Ethics Approval

The study was approved by the office of research affairs and the Ethical Committee of our Institution (approval number: RAC 2191111).

How to Cite

Kholaif, Naji, Lin Batha, Isra Elmahi, Sulaiman Alnaser, Sultan Alzaher, Norah Almallohi, Mosaad Alhussein, Dana Alhalees, and Ahmed Alshehri. 2024. “Transplantation of Heterozygous Familial Hypercholesterolemia Living Donor Liver Resulting in Early Myocardial Infarction: A Possible Dangerous Link”. Monaldi Archives for Chest Disease, January. https://doi.org/10.4081/monaldi.2024.2907.

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