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运动中急性营养性酮症对 IIIa 型糖原贮积病成人的影响具有表型特异性:一项由研究者发起的、随机、交叉研究。

Effects of acute nutritional ketosis during exercise in adults with glycogen storage disease type IIIa are phenotype-specific: An investigator-initiated, randomized, crossover study.

机构信息

Section of Metabolic Diseases, Beatrix Children's Hospital, University of Groningen, University Medical Center of Groningen, Groningen, The Netherlands.

National Hospital of the Faroe Islands, Medical Center, Tórshavn, Faroe Islands.

出版信息

J Inherit Metab Dis. 2021 Jan;44(1):226-239. doi: 10.1002/jimd.12302. Epub 2020 Sep 7.

Abstract

Glycogen storage disease type IIIa (GSDIIIa) is an inborn error of carbohydrate metabolism caused by a debranching enzyme deficiency. A subgroup of GSDIIIa patients develops severe myopathy. The purpose of this study was to investigate whether acute nutritional ketosis (ANK) in response to ketone-ester (KE) ingestion is effective to deliver oxidative substrate to exercising muscle in GSDIIIa patients. This was an investigator-initiated, researcher-blinded, randomized, crossover study in six adult GSDIIIa patients. Prior to exercise subjects ingested a carbohydrate drink (~66 g, CHO) or a ketone-ester (395 mg/kg, KE) + carbohydrate drink (30 g, KE + CHO). Subjects performed 15-minute cycling exercise on an upright ergometer followed by 10-minute supine cycling in a magnetic resonance (MR) scanner at two submaximal workloads (30% and 60% of individual maximum, respectively). Blood metabolites, indirect calorimetry data, and in vivo P-MR spectra from quadriceps muscle were collected during exercise. KE + CHO induced ANK in all six subjects with median peak βHB concentration of 2.6 mmol/L (range: 1.6-3.1). Subjects remained normoglycemic in both study arms, but delta glucose concentration was 2-fold lower in the KE + CHO arm. The respiratory exchange ratio did not increase in the KE + CHO arm when workload was doubled in subjects with overt myopathy. In vivo P MR spectra showed a favorable change in quadriceps energetic state during exercise in the KE + CHO arm compared to CHO in subjects with overt myopathy. Effects of ANK during exercise are phenotype-specific in adult GSDIIIa patients. ANK presents a promising therapy in GSDIIIa patients with a severe myopathic phenotype. TRIAL REGISTRATION NUMBER: ClinicalTrials.gov identifier: NCT03011203.

摘要

糖原贮积病 IIIa 型(GSDIIIa)是一种由分支酶缺乏引起的碳水化合物代谢先天性错误。GSDIIIa 患者的亚组会出现严重的肌病。本研究旨在探讨酮酯(KE)摄入引起的急性营养性酮症(ANK)是否能有效地将氧化底物输送到 GSDIIIa 患者的运动肌肉中。这是一项由研究者发起、研究者设盲、随机、交叉的研究,纳入了 6 名成年 GSDIIIa 患者。在运动前,受试者摄入碳水化合物饮料(~66g,CHO)或酮酯(395mg/kg,KE)+碳水化合物饮料(30g,KE+CHO)。受试者在直立式测功仪上进行 15 分钟的自行车运动,然后在磁共振(MR)扫描仪上进行 10 分钟的仰卧自行车运动,两个亚最大工作负荷(分别为个体最大负荷的 30%和 60%)。在运动过程中收集了血液代谢物、间接热量测定数据和股四头肌的体内 P-MR 谱。在所有 6 名受试者中,KE+CHO 诱导产生了中位峰值βHB 浓度为 2.6mmol/L(范围:1.6-3.1)的 ANK。在两种研究臂中,受试者均保持血糖正常,但 KE+CHO 臂中的葡萄糖浓度差值降低了 2 倍。在明显有肌病的受试者中,当工作负荷增加一倍时,KE+CHO 臂中的呼吸交换比并没有增加。与 CHO 相比,在明显有肌病的受试者中,KE+CHO 臂中的股四头肌能量状态在运动过程中表现出有利的变化。ANK 在 GSDIIIa 患者中的作用具有表型特异性。ANK 为 GSDIIIa 患者,尤其是严重肌病表型患者提供了一种很有前途的治疗方法。临床试验注册号:ClinicalTrials.gov 标识符:NCT03011203。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/063f/7891643/fde2e28c304e/JIMD-44-226-g001.jpg

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