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: 458
PDF_EARLY VIEW: 261
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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

Goldaracena N, Barbas AS. Living donor liver transplantation. Curr Opin Organ Transplant 2019;24:131-7. DOI: https://doi.org/10.1097/MOT.0000000000000610
Trotter JF. Selection of donors for living donor liver transplantation. Liver Transpl 2003;9:S2-7. DOI: https://doi.org/10.1053/jlts.2003.50221
Neuberger J. An update on liver transplantation: a critical review. J Autoimmun 2016;66:51-9. DOI: https://doi.org/10.1016/j.jaut.2015.08.021
Nikkilä K, Åberg F, Isoniemi H. Transmission of LDLR mutation from donor through liver transplantation resulting in hypercholesterolemia in the recipient. Am J Transplant 2014;14:2898-902. DOI: https://doi.org/10.1111/ajt.12961
Kholaif N, Mohamed TI, Alharbi IS, et al. Management and clinical outcomes of patients with homozygous familial hypercholesteremia in Saudi Arabia. Monaldi Arch Chest Dis 2023;93. doi:10.4081/monaldi.2023.2503 DOI: https://doi.org/10.4081/monaldi.2023.2503
Al-Rasadi K, Al-Waili K, Al-Sabti HA, et al. Criteria for diagnosis of familial hypercholesterolemia: a comprehensive analysis of the different guidelines, appraising their suitability in the Omani Arab population. Oman Med J 2014;29:85-91. DOI: https://doi.org/10.5001/omj.2014.22
Setia N, Saxena R, Arora A, Verma IC. Spectrum of mutations in homozygous familial hypercholesterolemia in India, with four novel mutations. Atherosclerosis 2016;255:31-6. DOI: https://doi.org/10.1016/j.atherosclerosis.2016.10.028
Gilroy R, Heronemus M, Schmitt T, Moriarty P. Donors with familial hypercholesterolemia and clinical outcome in liver transplant recipients. Transplantation 2014;98:796. DOI: https://doi.org/10.1097/00007890-201407151-02729
Popescu I, Habib N, Dima S, et al. Domino liver transplantation using a graft from a donor with familial hypercholesterolemia: seven-yr follow-up. Clin Transplant 2009;23:565-70. DOI: https://doi.org/10.1111/j.1399-0012.2008.00935.x
Liu C, Niu DM, Loong CC, et al. Domino liver graft from a patient with homozygous familial hypercholesterolemia. Pediatr Transplant 2010;14:E30-3. DOI: https://doi.org/10.1111/j.1399-3046.2009.01133.x
Ridker PM, Danielson E, Fonseca FA, et al. Rosuvastatin to prevent vascular events in men and women with elevated C-reactive protein. N Engl J Med 2008;359:2195-207. DOI: https://doi.org/10.1056/NEJMoa0807646
He K, Wang J, Shi H, et al. An interspecies study of lipid profiles and atherosclerosis in familial hypercholesterolemia animal models with low-density lipoprotein receptor deficiency. Am J Transl Res 2019;11:3116-27.

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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