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55例儿童和5例谷甾醇血症成人患者的临床、基因特征及治疗评估

Clinical, genetic profile and therapy evaluation of 55 children and 5 adults with sitosterolemia.

作者信息

Xia Yu, Duan Ying, Zheng Wanqi, Liang Lili, Zhang Huiwen, Luo Xiaomei, Gu Xuefan, Sun Yu, Xiao Bing, Qiu Wenjuan

机构信息

Department of Pediatric Endocrinology and Genetic Metabolism, Xinhua Hospital, Shanghai Institute of Pediatric Research, School of Medicine, Shanghai Jiao Tong University, 1665 Kong Jiang Road, Shanghai 200092, China.

Department of Pediatric Endocrinology and Genetic Metabolism, Xinhua Hospital, Shanghai Institute of Pediatric Research, School of Medicine, Shanghai Jiao Tong University, 1665 Kong Jiang Road, Shanghai 200092, China.

出版信息

J Clin Lipidol. 2022 Jan-Feb;16(1):40-51. doi: 10.1016/j.jacl.2021.11.015. Epub 2021 Dec 6.

Abstract

BACKGROUND

Sitosterolemia is a rare autosomal recessive disease characterized by phytosterol accumulation in the blood and tissues. However, the detailed clinical and genetic spectra are lacking.

OBJECTIVE

To describe and compare the clinical, biochemical, genetic, therapeutic, and follow-up characteristics of 55 pediatric and five adult sitosterolemia patients.

METHODS

Clinical, genetic and therapeutic data from 60 patients at Xinhua Hospital from January 2016 to June 2021 were retrospectively collected.

RESULTS

Pediatric patients' manifestations included xanthomas(93%), hematological disorders(30%), arthralgia(24%), splenomegaly(11%), atherosclerosis(10%). Adult patients had symptoms such as atherosclerosis(5/5), xanthomas(4/5), hematological disorders(3/5), arthralgia(3/5), splenomegaly(3/5). Elevated total cholesterol(TC) and low-density lipoprotein cholesterol(LDL-C) were observed in 96% patients (pediatric 98%, adult 3/4), and phytosterol levels in 100% patients. The age of onset was also negatively correlated with blood TC (P < 0.0001, r = -0.5548) and LDL-C (P = 0.0001, r = -0.4859) levels. Targeted treatments resulted in symptomatic remission(pediatric 96%, adult 4/5), and significantly decreased lipid and phytosterol levels(all P<0.05). In the dietary-therapy cohort(n=34), blood lipid levels decreased(all P<0.05). In the 13 pediatric patients from the dietary-therapy cohort who switched from dietary to combination therapy with ezetimibe, dietary therapy decreased TC and LDL-C levels by 54% and 52%, and ezetimibe further decreased them by 18% and 20%, respectively. Further, we identified 15 novel ABCG5/ABCG8 variants.

CONCLUSIONS

This study expands the clinical and genetic spectra of sitosterolemia. The low-phytosterol diet is the cornerstone of sitosterolemia treatment. Ezetimibe can further decrease blood lipid levels and increase daily dietary phytosterol tolerance.

摘要

背景

谷甾醇血症是一种罕见的常染色体隐性疾病,其特征是血液和组织中植物甾醇蓄积。然而,详细的临床和基因谱尚缺乏。

目的

描述并比较55例儿童和5例成人谷甾醇血症患者的临床、生化、基因、治疗及随访特征。

方法

回顾性收集2016年1月至2021年6月新华医院60例患者的临床、基因和治疗数据。

结果

儿童患者的表现包括黄色瘤(93%)、血液系统疾病(30%)、关节痛(24%)、脾肿大(11%)、动脉粥样硬化(10%)。成人患者有动脉粥样硬化(5/5)、黄色瘤(4/5)、血液系统疾病(3/5)、关节痛(3/5)、脾肿大(3/5)等症状。96%的患者观察到总胆固醇(TC)和低密度脂蛋白胆固醇(LDL-C)升高(儿童98%,成人3/4),100%的患者植物甾醇水平升高。发病年龄也与血液TC水平(P<0.0001,r=-0.5548)和LDL-C水平(P=0.0001,r=-0.4859)呈负相关。靶向治疗导致症状缓解(儿童96%,成人4/5),并显著降低血脂和植物甾醇水平(所有P<0.05)。在饮食治疗队列(n=34)中,血脂水平下降(所有P<0.05)。在饮食治疗队列中从饮食治疗转为依折麦布联合治疗的13例儿童患者中,饮食治疗使TC和LDL-C水平分别降低了54%和52%,依折麦布进一步使它们分别降低了18%和20%。此外,我们鉴定出15种新的ABCG5/ABCG8变异体。

结论

本研究扩展了谷甾醇血症的临床和基因谱。低植物甾醇饮食是谷甾醇血症治疗的基石。依折麦布可进一步降低血脂水平并提高每日饮食中植物甾醇的耐受性。

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