Perioperative Management and Clinical Outcomes of Liver Transplantation for Children with Homozygous Familial Hypercholesterolemia

被引:6
作者
Qiu, Huan-Rong [1 ]
Zhang, Liang [1 ]
Zhu, Zhi-Jun [2 ]
机构
[1] Capital Med Univ, Beijing Friendship Hosp, Dept Anesthesiol, Beijing 100050, Peoples R China
[2] Capital Med Univ, Beijing Friendship Hosp, Liver Transplantat Ctr, Natl Clin Res Ctr Digest Dis, Beijing 100050, Peoples R China
来源
MEDICINA-LITHUANIA | 2022年 / 58卷 / 10期
基金
中国国家自然科学基金;
关键词
homozygous familial hypercholesterolemia; perioperative management; liver transplantation; children; cardiovascular comorbidities; postoperative complications; survival; DOUBLE-BLIND; EFFICACY; SAFETY; INHIBITION; GUIDANCE; THERAPY; ASSOCIATION; ADOLESCENTS; ALIROCUMAB; EVOLOCUMAB;
D O I
10.3390/medicina58101430
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and Objectives: Liver transplantation (LT) has been accepted as a life-saving option as a last resort for children with homozygous familial hypercholesterolemia (HoFH). Perioperative management of LT for HoFH poses extra challenges for clinicians largely due to premature atherosclerotic cardiovascular diseases (ASCVDs). We aimed to analyze our data of pediatric LT recipients with HoFH, with special attention paid to perioperative management and clinical outcomes. Materials and Methods: After obtaining approval from the local ethics committee, the clinical data of pediatric patients with HoFH who underwent LT at our institution between January 2014 and February 2021 were retrospectively studied. Results: Six pediatric LT recipients with HoFH were included in the analysis. Although ASCVDs were common before LT, all children with HoFH survived the perioperative period without in-hospital mortality. However, one patient experienced acute myocardial infarction two months following LT and was successfully treated with medical interventions. Post-LT metabolic improvement was shown by declines in serum total cholesterol (TC) and low-density lipoprotein cholesterol (LDL-C) levels in the early post-LT period (for TC: 14.7 +/- 3.2 mmol/L vs. 5.5 +/- 1.8 mmol/L, p < 0.001; for LDL-C: 10.6 +/- 2.2 mmol/L vs. 3.6 +/- 1.2 mmol/L, p < 0.001, respectively) and at the last follow-up (for TC: 14.7 +/- 3.2 mmol/L vs. 4.5 +/- 0.9 mmol/L, p = 0.001; for LDL-C: 10.6 +/- 2.2 mmol/L vs. 2.8 +/- 0.6 mmol/L, p = 0.001, respectively). Dietary restrictions could be lifted after LT. However, three patients required restarting lipid-lowering therapy after LT due to suboptimal LDL-C levels and progression of ASCVDs. Conclusions: Our data suggest that LT can be a safe and feasible therapeutic option for well-selected patients with HoFH, offering relaxed dietary restrictions and remarkable reductions in LDL-C levels. However, concerns remain regarding progression of ASCVDs after LT.
引用
收藏
页数:11
相关论文
共 50 条
[1]   Liver Transplantation for Homozygous Familial Hypercholesterolemia [J].
Ishigaki, Yasushi ;
Kawagishi, Naoki ;
Hasegawa, Yutaka ;
Sawada, Shojiro ;
Katagiri, Hideki ;
Satomi, Susumu ;
Oikawa, Shinichi .
JOURNAL OF ATHEROSCLEROSIS AND THROMBOSIS, 2019, 26 (02) :121-127
[2]   Impact of the characteristics of patients and their clinical management on outcomes in children with homozygous familial hypercholesterolemia [J].
Al-Shaikh, AM ;
Abdullah, MH ;
Barclay, A ;
Cullen-Dean, G ;
McCrindle, BW .
CARDIOLOGY IN THE YOUNG, 2002, 12 (02) :105-112
[3]   Clinical Management of Familial Hypercholesterolemia in Children [J].
Widhalm, Kurt ;
Fallmann, Karin .
CURRENT PEDIATRIC REVIEWS, 2024,
[4]   Coronary artery disease in a child with homozygous familial hypercholesterolemia: Regression after liver transplantation [J].
Cephus, Constance E. ;
Qureshi, Athar M. ;
Tejtel, S. Kristen Sexson ;
Alam, Mahboob ;
Moodie, Douglas S. .
JOURNAL OF CLINICAL LIPIDOLOGY, 2019, 13 (06) :880-886
[5]   LIVER-TRANSPLANTATION FOR HOMOZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA [J].
REVELL, SP ;
NOBLEJAMIESON, G ;
JOHNSTON, P ;
RASMUSSEN, A ;
JAMIESON, N ;
BARNES, ND .
ARCHIVES OF DISEASE IN CHILDHOOD, 1995, 73 (05) :456-458
[6]   The clinical and molecular diversity of homozygous familial hypercholesterolemia in children: Results from the GeneTics of clinical homozygous hypercholesterolemia (GoTCHA) study [J].
Luirink, Ilse K. ;
Braamskamp, Marjet J. A. M. ;
Wiegman, Albert ;
Hartgers, Merel L. ;
Sjouke, Barbara ;
Defesche, Joep C. ;
Hovingh, G. Kees .
JOURNAL OF CLINICAL LIPIDOLOGY, 2019, 13 (02) :272-278
[7]   Lomitapide for the Management of Homozygous Familial Hypercholesterolemia [J].
deGoma, Emil M. .
REVIEWS IN CARDIOVASCULAR MEDICINE, 2014, 15 (02) :109-118
[8]   Liver transplantation for homozygous familial hypercholesterolemia: Cure for a genetic disease? [J].
Katzmann, Julius L. ;
Laufs, Ulrich .
ATHEROSCLEROSIS, 2023, 387
[9]   Liver transplantation for homozygous familial hypercholesterolemia: a retrospective analysis from Chinese experience [J].
Zhan, Hao-Su ;
Wei, Lin ;
Qu, Wei ;
Zeng, Zhi-Gui ;
Liu, Ying ;
Tan, Yu-Le ;
Wang, Jun ;
Zhang, Liang ;
He, En-Hui ;
Zhou, Guang-Peng ;
Zhang, Hai-Ming ;
Zhu, Zhi-Jun ;
Sun, Li-Ying .
ORPHANET JOURNAL OF RARE DISEASES, 2025, 20 (01)
[10]   Liver transplantation as a treatment option for three siblings with homozygous familial hypercholesterolemia [J].
Kucukkartallar, Tevfik ;
Yankol, Yucel ;
Kanmaz, Turan ;
Topaloglu, Serdar ;
Acarli, Koray ;
Kalayoglu, Munci .
PEDIATRIC TRANSPLANTATION, 2011, 15 (03) :281-284