Is Liver Transplantation Alone an Effective Treatment for Homozygotic Familial Hypercholesterolemia in Children?

被引:0
作者
Dagli, Hatice Yilmaz [1 ]
Artan, Reha [1 ]
Civan, Dudu Duygu [1 ]
Aydemir, Nurel Inan [1 ]
Yilmaz, Aygen [1 ]
机构
[1] Akdeniz Univ, Dept Pediat Gastroenterol, Antalya, Turkiye
关键词
child; familial hypercholesterolemia; liver transplantation; LOW-DENSITY-LIPOPROTEIN; CONSENSUS PANEL; ATHEROSCLEROSIS; CHOLESTEROL; APHERESIS; PATIENT; IMPACT;
D O I
10.1111/petr.14853
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Aim: To examine the long- term results and treatment effectiveness of liver transplantation (LT) in the treatment of homozygous familial hypercholesterolemia (HoFH) in children and adolescents. Method: Patients who underwent LT due to HoFH between 2007 and 2023 were included in the study. The patients' demographic data, clinical findings, preoperative and postoperative laboratory examinations, transplantation complications, and postoperative disease courses were evaluated. Results: There were five boys with an average age of 6.2 (median: 6, range 4-10) years in the study. The average total cholesterol level of the patients before transplantation was 923 (median: 950, range: 780-1002) mg/dL and the average LDL- cholesterol level was 864 (median: 852, range: 770-957) mg/dL. No patients died of transplant- related complications. After an average follow- up of 9.2 (median: 9, range: 1.5-16) years, the average total cholesterol level of the patients was 197 (median: 164, range: 137-359) mg/dL, and the average LDL- cholesterol level was 138 (median: 92, range: 85-313) mg/dL. Four (80%) patients developed atherosclerotic cardiovascular disease during follow- up, and two (40%) died of this cause. Conclusion: LT in the treatment of HoFH did not help our patients reach the target LDL- cholesterol level after transplantation and did not prevent the development of cardiovascular disease. Therefore, LT alone is not curative in the treatment of HoFH.
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共 34 条
[1]  
Agarwal Arnav, 2016, World J Transplant, V6, P125, DOI 10.5500/wjt.v6.i1.125
[2]   Unusual Indications for a Liver Transplant: A Single-Center Experience [J].
Akdur, Aydincan ;
Kirnap, Mahir ;
Soy, Ebru H. Ayvazoglu ;
Ozcay, Figen ;
Moray, Gokhan ;
Arslan, Gulnaz ;
Haberal, Mehmet .
EXPERIMENTAL AND CLINICAL TRANSPLANTATION, 2017, 15 :128-132
[3]   Is Liver Transplant Curative in Homozygous Familial Hypercholesterolemia? A Review of Nine Global Cases [J].
Al Dubayee, Mohammed ;
Kayikcioglu, Meral ;
van Lennep, Jeanine Roeters ;
Hergli, Nadia ;
Mata, Pedro .
ADVANCES IN THERAPY, 2022, 39 (06) :3042-3057
[4]   Phenotypical, Clinical, and Molecular Aspects of Adults and Children With Homozygous Familial Hypercholesterolemia in Iberoamerica [J].
Alves, Ana Catarina ;
Alonso, Rodrigo ;
Diaz-Diaz, Jose Luis ;
Medeiros, Ana Margarida ;
Jannes, Cinthia E. ;
Merchan, Alonso ;
Vasques-Cardenas, Norma A. ;
Cuevas, Ada ;
Chacra, Ana Paula ;
Krieger, Jose E. ;
Arroyo, Raquel ;
Arrieta, Francisco ;
Schreier, Laura ;
Corral, Pablo ;
Banares, Virginia G. ;
Araujo, Maria B. ;
Bustos, Paula ;
Asenjo, Sylvia ;
Stoll, Mario ;
Dell'Oca, Nicolas ;
Reyes, Maria ;
Ressia, Andres ;
Campo, Rafael ;
Magana-Torres, Maria T. ;
Metha, Roopa ;
Aguilar-Salinas, Carlos A. ;
Ceballos-Macias, Jose J. ;
Ruiz Morales, Alvaro J. ;
Mata, Pedro ;
Bourbon, Mafalda ;
Santos, Raul D. .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2020, 40 (10) :2508-2515
[5]   LIVER-TRANSPLANTATION TO PROVIDE LOW-DENSITY-LIPOPROTEIN RECEPTORS AND LOWER PLASMA-CHOLESTEROL IN A CHILD WITH HOMOZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA [J].
BILHEIMER, DW ;
GOLDSTEIN, JL ;
GRUNDY, SM ;
STARZL, TE ;
BROWN, MS .
NEW ENGLAND JOURNAL OF MEDICINE, 1984, 311 (26) :1658-1664
[6]   Inhibition of microsomal triglyceride transfer protein in familial hypercholesterolemia [J].
Cuchel, Marina ;
Bloedon, LeAnne T. ;
Szapary, Philippe O. ;
Kolansky, Daniel M. ;
Wolfe, Megan L. ;
Sarkis, Antoine ;
Millar, John S. ;
Ikewaki, Katsunori ;
Siegelman, Evan S. ;
Gregg, Richard E. ;
Rader, Daniel J. .
NEW ENGLAND JOURNAL OF MEDICINE, 2007, 356 (02) :148-156
[7]   Homozygous familial hypercholesterolaemia: new insights and guidance for clinicians to improve detection and clinical management. A position paper from the Consensus Panel on Familial Hypercholesterolaemia of the European Atherosclerosis Society [J].
Cuchel, Marina ;
Bruckert, Eric ;
Ginsberg, Henry N. ;
Raal, Frederick J. ;
Santos, Raul D. ;
Hegele, Robert A. ;
Kuivenhoven, Jan Albert ;
Nordestgaard, Borge G. ;
Descamps, Olivier S. ;
Steinhagen-Thiessen, Elisabeth ;
Tybjrg-Hansen, Anne ;
Watts, Gerald F. ;
Averna, Maurizio ;
Boileau, Catherine ;
Boren, Jan ;
Catapano, Alberico L. ;
Defesche, Joep C. ;
Hovingh, G. Kees ;
Humphries, Steve E. ;
Kovanen, Petri T. ;
Masana, Luis ;
Pajukanta, Paivi ;
Parhofer, Klaus G. ;
Ray, Kausik K. ;
Stalenhoef, Anton F. H. ;
Stroes, Erik ;
Taskinen, Marja-Riitta ;
Wiegman, Albert ;
Wiklund, Olov ;
Chapman, M. John .
EUROPEAN HEART JOURNAL, 2014, 35 (32) :2146-U100
[8]   Early-onset plasmapheresis and LDL-apheresis provide better disease control for pediatric homozygous familial hypercholesterolemia than HMG-CoA reductase inhibitors and ameliorate atherosclerosis [J].
Dann, Eldad J. ;
Shamir, Raanan ;
Mashiach, Tatiana ;
Shaoul, Ron ;
Badian, Alla ;
Stravets, Tselestina ;
Kerzman, Yelena ;
Finkelbaum, Svetlana ;
Gaitini, Diana ;
Lorber, Avraham ;
Bonstein, Lilach .
TRANSFUSION AND APHERESIS SCIENCE, 2013, 49 (02) :268-277
[9]   Comparison of two low-density lipoprotein apheresis systems in patients with homozygous familial hypercholesterolemia [J].
Drouin-Chartier, Jean-Philippe ;
Tremblay, Andre J. ;
Bergeron, Jean ;
Pelletier, Maude ;
Laflamme, Nathalie ;
Lamarche, Benoit ;
Couture, Patrick .
JOURNAL OF CLINICAL APHERESIS, 2016, 31 (04) :359-367
[10]   Rapidly progressive atherosclerosis after domino liver transplantation from a teenage donor with homozygous familial hypercholesterolemia [J].
Golbus, Jessica R. ;
Farhat, Linda ;
Fontana, Robert J. ;
Rubenfire, Melvyn .
JOURNAL OF CLINICAL LIPIDOLOGY, 2017, 11 (05) :1284-1288