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35例有机酸代谢紊乱患者的骨科问题

Orthopaedic Problems in 35 Patients With Organic Acid Disorders.

作者信息

Prasad Niyathi, Gottlich Caleb, Nhan Derek, Hamosh Ada, Sponseller Paul D

机构信息

Departments of Orthopaedic Surgery.

Genetic Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD.

出版信息

J Pediatr Orthop. 2021 Jul 1;41(6):e457-e463. doi: 10.1097/BPO.0000000000001812.

Abstract

INTRODUCTION

Organic acid disorders (OADs) are a subset of inborn errors of metabolism that result in a toxic accumulation of organic acids in the body, which can lead to metabolic derangements and encephalopathy. Patients with these disorders are managed by a team of biochemical geneticists and metabolic nutritionists. However, subspecialists such as neurologists and orthopaedic surgeons are often needed to help manage the sequelae of the metabolic derangements. The breadth of orthopaedic sequelae of these disease states is poorly understood. Herein, we describe orthopaedic problems associated with 5 types of OAD most commonly seen at our institution: maple syrup urine disease, methylmalonic aciduria, propionic aciduria, pyruvate dehydrogenase deficiency, and glutaric aciduria type 1.

METHODS

We retrospectively reviewed medical records of 35 patients with an OAD who were seen at our academic tertiary care center from May 1999 to May 2020. Patients were grouped into cohorts according to OAD type and analyzed for orthopaedic presentations of hip, knee, or foot disorders, presence and severity of scoliosis, history of fracture, movement disorders, and osteopenia/osteoporosis.

RESULTS

Of the 35 patients, 13 had maple syrup urine disease, 12 had methylmalonic aciduria, 4 had propionic aciduria, 4 had pyruvate dehydrogenase deficiency, and 2 had glutaric aciduria type 1. Associated orthopaedic problems included spasticity causing neuromuscular scoliosis and/or hip subluxation or dislocation (10 patients), fractures (7 patients), and osteopenia/osteoporosis (7 patients). Overall, 22 of 35 patients had some orthopaedic condition.

CONCLUSIONS

Most in this cohort of patients with OAD also had an orthopaedic abnormality. It is important for physicians treating these patients to understand their propensity for musculoskeletal problems. When treating patients with OAD, it is important to initiate and maintain communication with specialists in several disciplines and to develop collaborative treatments for this unique population.

LEVEL OF EVIDENCE

Level IV-prognostic study.

摘要

引言

有机酸代谢紊乱(OADs)是先天性代谢缺陷的一个子集,会导致体内有机酸的毒性蓄积,进而引发代谢紊乱和脑病。患有这些疾病的患者由生化遗传学家和代谢营养学家团队进行管理。然而,通常还需要神经科医生和骨科医生等专科医生来协助处理代谢紊乱的后遗症。人们对这些疾病状态的骨科后遗症的广度了解不足。在此,我们描述了与我院最常见的5种OAD相关的骨科问题:枫糖尿症、甲基丙二酸血症、丙酸血症、丙酮酸脱氢酶缺乏症和1型戊二酸血症。

方法

我们回顾性分析了1999年5月至2020年5月在我院学术三级医疗中心就诊的35例OAD患者的病历。根据OAD类型将患者分组,并分析髋、膝或足部疾病的骨科表现、脊柱侧弯的存在及严重程度、骨折史、运动障碍以及骨质减少/骨质疏松情况。

结果

35例患者中,13例患有枫糖尿症,12例患有甲基丙二酸血症,4例患有丙酸血症,4例患有丙酮酸脱氢酶缺乏症,2例患有1型戊二酸血症。相关的骨科问题包括导致神经肌肉型脊柱侧弯和/或髋关节半脱位或脱位的痉挛(10例患者)、骨折(7例患者)以及骨质减少/骨质疏松(7例患者)。总体而言,35例患者中有22例存在某种骨科疾病。

结论

该队列中大多数患有OAD的患者也存在骨科异常。治疗这些患者的医生了解他们发生肌肉骨骼问题的倾向非常重要。在治疗OAD患者时,重要的是启动并维持与多个学科专家的沟通,并为这一特殊人群制定协作治疗方案。

证据级别

IV级——预后研究。

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