脉络膜和视网膜旋转萎缩(GACR)的新见解:一项队列研究。

IF 4.2 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM Journal of Inherited Metabolic Disease Pub Date : 2025-01-01 DOI:10.1002/jimd.12842
Berith M Balfoort, Filip Van den Broeck, Camiel J F Boon, Martijn C G J Brouwers, Roselie M H Diederen, Preet Dhillon, Peter M van Hasselt, Bregje Jaeger, Jessica S Karuntu, Alexander J M Rennings, Francjan J van Spronsen, Corrie Timmer, Margreet A E M Wagenmakers, Julie De Zaeytijd, Bart P Leroy, Andreas Schulze, Clara D van Karnebeek, Marion M Brands
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引用次数: 0

摘要

脉络膜和视网膜旋转萎缩(GACR, OMIM #258870)是一种罕见的遗传性代谢疾病,以进行性脉络膜视网膜变性和高鸟氨酸血症为特征。目前的治疗方式可能会减缓疾病进展,但在预防失明方面并不成功。为了进行试验开发,需要增加对临床表型和当前治疗结果的了解。本研究中,我们分析了27例GACR患者。纳入时的中位年龄为24岁(范围8-58岁),诊断时的中位年龄为14岁(范围0-42岁)。症状开始于平均9岁(范围0-21岁)。混合模型分析显示,膳食天然蛋白质摄入量与血浆鸟氨酸水平之间存在显著关联。鸟氨酸随着年龄的增长而显著增加,与膳食天然蛋白质摄入量无关。随着时间的推移,我们发现鸟氨酸水平与最佳矫正视力之间没有统计学上的显著关联。在10岁以下开始自然限制蛋白质饮食的患者与年龄较晚的患者相比,VF结果更好。磁共振光谱学用于评估脑肌酸缺乏症,其中15/20的患者中存在肌酸缺乏症,其中10人当时补充了肌酸。最后,使用密歇根视网膜变性问卷,我们首次深入了解了GACR患者报告的视力相关残疾,并表明较高的中央凹敏感性与较低的感知残疾相关。综上所述,本研究对GACR的表型、基因型、生物化学和治疗效果提供了深入的了解,可用于护理路径和临床试验设计。
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Novel Insights Into Gyrate Atrophy of the Choroid and Retina (GACR): A Cohort Study.

Gyrate atrophy of the choroid and retina (GACR, OMIM #258870) is a rare inherited metabolic disorder characterized by progressive chorioretinal degeneration and hyperornithinemia. Current therapeutic modalities potentially slow disease progression but are not successful in preventing blindness. To allow for trial development, increased knowledge of the clinical phenotype and current therapeutic outcomes is required. In this study, we analyzed 27 patients with GACR. The median age at inclusion was 24 years (range 8-58), with a median age at diagnosis of 14 years (range 0-42). Symptoms began at a mean age of 9 years (range 0-21). Mixed-models analysis showed a significant association between dietary natural protein intake and plasma ornithine levels. Ornithine increased significantly with age, independent of dietary natural protein intake. We found no statistically significant association between ornithine levels and best-corrected visual acuity over time. Patients who started a natural protein-restricted diet below 10 years of age had better VF outcomes compared to patients that started at a later age. MR spectroscopy was used to asses cerebral creatine deficiency, which was present in 15/20 patients, of whom 10 were supplemented with creatine at the time. Finally, using the Michigan Retinal Degeneration Questionnaire, we provided a first insight into the vision-related disability reported by patients with GACR and showed that higher foveal sensitivity was associated with less perceived disability. To conclude, this study provides insights into the phenotype, genotype, biochemistry, and treatment effects of GACR, which can be used for care pathways and clinical trial design.

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来源期刊
Journal of Inherited Metabolic Disease
Journal of Inherited Metabolic Disease 医学-内分泌学与代谢
CiteScore
9.50
自引率
7.10%
发文量
117
审稿时长
4-8 weeks
期刊介绍: The Journal of Inherited Metabolic Disease (JIMD) is the official journal of the Society for the Study of Inborn Errors of Metabolism (SSIEM). By enhancing communication between workers in the field throughout the world, the JIMD aims to improve the management and understanding of inherited metabolic disorders. It publishes results of original research and new or important observations pertaining to any aspect of inherited metabolic disease in humans and higher animals. This includes clinical (medical, dental and veterinary), biochemical, genetic (including cytogenetic, molecular and population genetic), experimental (including cell biological), methodological, theoretical, epidemiological, ethical and counselling aspects. The JIMD also reviews important new developments or controversial issues relating to metabolic disorders and publishes reviews and short reports arising from the Society''s annual symposia. A distinction is made between peer-reviewed scientific material that is selected because of its significance for other professionals in the field and non-peer- reviewed material that aims to be important, controversial, interesting or entertaining (“Extras”).
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