Treatment with L-citrulline and metformin in Duchenne muscular dystrophy: study protocol for a single-centre, randomised, placebo-controlled trial.
デュシェンヌ型筋ジストロフィーにおけるL-シトルリンとメトホルミンの治療:単施設・無作為化・プラセボ対照試験の試験計画 (機械翻訳の邦題)
記録の確認項目
- 研究デザイン
- ランダム化比較試験
- 対象
- ヒト
- 出版年
- 2016
- 出典
- doi.org
- 抄録の表示
- 表示あり
- 出版状態
- 有効な記録
- 状態確認日
- 2026/08/17
- 収集日
- 2026/08/03
- 鮮度
- 確認期限内
- 確認段階
- 自動処理
- 記録状態
- 公開
日本語要約(機械生成)
デュシェンヌ型筋ジストロフィー(DMD)はX連鎖劣性遺伝性疾患で、現在の治療は支持療法に限られる。本試験は、L-シトルリンとメトホルミンの併用療法がプラセボより優れるかを検証する無作為化二重盲検プラセボ対照試験である。対象はスイス、ドイツ、オーストリアの登録患者から募集する歩行可能なDMD患者40〜50例。26週間の治療で、主要評価項目はMotor Function Measure(MFM)D1サブスコアの変化、副次評価項目は運動機能、筋力、定量的筋MRIによる筋脂肪分画、安全性、バイオマーカーなど。また、健常男児10〜20例で筋代謝とミトコンドリア機能を比較する。本試験は6か月間の治療が運動機能低下と筋変性の予防に有効かを検討する。
この要約は公開抄録のみを根拠にAIが機械的に生成したものです。正確な内容は原文を確認してください。
抄録
Background: Duchenne muscular dystrophy (DMD) is an X-linked recessive disease that affects 1 in 3500-6000 male births. Despite broad research aiming to improve muscle function as well as heart and brain function, sufficient therapeutic efficacy has not yet been achieved and current therapeutic management is still supportive. In a recent pilot trial, oral treatment with L-arginine and metformin showed consistent changes of muscular metabolism both in vitro and in vivo by raising NO levels and expression of mitochondrial proteins in the skeletal muscle tissue of patients with DMD. This randomised, double-blind, placebo-controlled trial aims to demonstrate the superiority of L-citrulline and metformin therapy over placebo in DMD patients with regard to the Motor Function Measure (MFM) D1 subscore (primary endpoint) as well as additional clinical and subclinical tests.Methods/design: A total of 40-50 ambulant patients with DMD will be recruited at the outpatient department of the University of Basel Children's Hospital (Switzerland), as well as from the DMD patient registries of Switzerland, Germany and Austria. Patients will be randomly allocated to one of the two arms of the study and will receive either a combination of L-citrulline and metformin or placebo for 26 weeks. Co-medication with glucocorticoids is allowed. The primary endpoint is the change of the MFM D1 subscore from baseline to week 26 under L-citrulline and metformin therapy. Secondary endpoints will include the motor function measure (MFM) and its items and subscores, the 6-minute walking test, timed function tests and quantitative muscle testing. Furthermore, quantitative muscle MRI assessment to evaluate the muscle fat fraction as well as safety and biomarker laboratory analyses from blood will be included. For comparison, muscle metabolism and mitochondrial function will be analysed in 10-20 healthy age-matched male children.Discussion: The aim of this study is to test if a 6-month treatment of a combination of L-citrulline and metformin is more effective than placebo in preventing loss of motor function and muscle degeneration in DMD. The MFM D1 subscore is used as a clinical outcome measure and a quantitative muscle MRI assessment as the surrogate outcome measure of fatty muscle degeneration.Trial registration: ClinicalTrials.gov: NCT01995032 . Registered on 20 November 2013.
MeSH
DOI 10.1186/s13063-016-1503-1
PMID 27488051
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