Choline supplementation in classic homocystinuria: impact on homocysteine and hepatic steatosis.

IF 3.1 3区 医学 Q1 PEDIATRICS
Sevde Kahraman, Asuman Gedikbasi, Meryem Karaca, Celal Caner Ercan, Mehmet Cihan Balci, Gulden Gokcay
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Abstract

Background: Classic homocystinuria is a sulfur metabolism disorder caused by cystathionine beta synthase (CBS) deficiency. The primary aim of treatment is to maintain plasma homocysteine (Hcy) concentration within the target range. This study investigated choline status and the effect of choline supplementation in CBS-deficient homocystinuria patients with elevated Hcy levels despite standard therapy.

Methods: Fifteen CBS-deficient homocystinuria patients and 20 controls with normal Hcy levels were enrolled. The study group received 1000 mg/day of choline bitartrate for 8 weeks. The control group was not given any supplements. Anthropometric measurements, biochemical tests, liver magnetic resonance proton density fat fraction imaging, and food consumption records of the participants in the study group were evaluated at baseline and at the end of the study.

Results: All participants demonstrated inadequate dietary choline intake. Choline supplementation significantly increased plasma free and total choline levels (p < 0.01) and reduced average plasma Hcy levels from 123.1 ± 52.2 to 61.1 ± 42.9 µmol/L (p < 0.01). In three of the four patients with hepatic steatosis at the beginning of the study, the condition regressed with choline supplementation.

Conclusion: In conclusion, choline supplementation should be considered in CBS-deficient homocystinuria patients with low plasma choline and high Hcy levels despite standard therapy.

Impact: Choline supplementation further decreases plasma homocysteine levels in patients with classic homocystinuria who still have elevated plasma homocysteine levels on standard therapy. Choline supplementation led to a remarkable surge in plasma free and total choline levels, which marked a significant breakthrough for classic homocystinuria patients. Remarkably, choline supplementation reversed hepatic steatosis in three out of four patients, highlighting its powerful therapeutic potential.

典型同型半胱氨酸尿患者补充胆碱:对同型半胱氨酸和肝脂肪变性的影响。
背景:典型同型半胱氨酸尿是一种由胱硫氨酸-合成酶(CBS)缺乏引起的硫代谢紊乱。治疗的主要目的是维持血浆同型半胱氨酸(Hcy)浓度在目标范围内。本研究调查了在标准治疗后Hcy水平升高的cbs缺陷型同型半胱氨酸尿患者的胆碱状态和补充胆碱的效果。方法:选取15例cbs缺陷型同型半胱氨酸尿患者和20例Hcy正常的对照组。研究组接受1000mg /天的双酒石酸胆碱治疗,持续8周。对照组不给予任何补充。在基线和研究结束时,对研究组参与者的人体测量、生化测试、肝脏磁共振质子密度脂肪分数成像和食物消耗记录进行评估。结果:所有参与者都表现出饮食胆碱摄入量不足。结论:对于缺乏cbs的同型半胱氨酸尿患者,尽管接受了标准治疗,但仍存在血浆胆碱水平低、Hcy水平高的情况,应考虑补充胆碱。影响:补充胆碱进一步降低经典同型半胱氨酸尿患者的血浆同型半胱氨酸水平,这些患者在标准治疗中仍有血浆同型半胱氨酸水平升高。补充胆碱导致血浆游离胆碱和总胆碱水平显著上升,这标志着典型同型半胱氨酸尿患者的重大突破。值得注意的是,四分之三的患者补充胆碱可以逆转肝脂肪变性,突出了其强大的治疗潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pediatric Research
Pediatric Research 医学-小儿科
CiteScore
6.80
自引率
5.60%
发文量
473
审稿时长
3-8 weeks
期刊介绍: Pediatric Research publishes original papers, invited reviews, and commentaries on the etiologies of children''s diseases and disorders of development, extending from molecular biology to epidemiology. Use of model organisms and in vitro techniques relevant to developmental biology and medicine are acceptable, as are translational human studies
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