How can we design a proper trial for vitamin D treatment of diseases? Facts and numbers

IF 8.9 1区 医学 Journal of Cachexia, Sarcopenia and Muscle Pub Date : 2023-04-18 DOI:10.1002/jcsm.13200
Shuang Zheng, Zhaohua Zhu, Changhai Ding
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Abstract

Vitamin D deficiency is a globally common situation and closely related with many chronic diseases. It is a hot topic to examine if vitamin D supplementation is effective for the treatment of diseases, and there have been dozens of clinical trials published in recent years. However, most studies have not proved the extra-skeletal benefits of vitamin D supplementation on these diseases. Some inherent shortcomings of these trials, such as inclusion with vitamin D-sufficient and obese participants, low response rate from participants and the insensitive changes in chosen outcomes over a shorter period, may be main reasons why most studies have yet to demonstrate effects of vitamin D supplementation. In this editorial, we aim to discuss the perspectives on how can we design a proper trial for vitamin D treatment of diseases based on the evidence-based practice framework PICOS (participants, intervention, control, outcomes and study design) in the future. First, right participants should be chosen, which is crucial for the success of vitamin D clinical trials. Participants with vitamin D sufficiency (e.g., baseline 25(OH)D of >50 nmol/L), obesity (e.g., body mass index > 30 kg/m2) and/or high vitamin D response index could be excluded from the trials. Second, intervention with vitamin D in right forms or dosages should be used. Vitamin D3 supplementation with appropriate dosages that keep 25(OH)D levels between 75 and 100 nmol/L is recommended. Third, ‘contamination’ in the control groups needs to pay attention. To diminish this, it is ideal to include participants less interfered by sun exposure (such as living in places at a high latitude) or with greater compliance (less interference by supplemental vitamin D-containing nutrients). Fourth, the outcome measures should be sensitive to change to avoid type II error. For outcomes such as bone density, radiographic osteoarthritis and cardiovascular diseases, follow-up period of 3–5 years may be required to observe the changes. Last, precision clinical trials may be the only way to prove the benefits of vitamin D supplementation.

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我们如何设计一个适当的维生素D治疗疾病的试验?事实和数据
维生素D缺乏症是一种全球普遍现象,与许多慢性疾病密切相关。研究补充维生素D是否对治疗疾病有效是一个热门话题,近年来已经发表了数十项临床试验。然而,大多数研究并没有证明补充维生素D对这些疾病的骨骼外益处。这些试验的一些固有缺陷,例如纳入了维生素D充足和肥胖的参与者,参与者的低反应率以及选择的结果在较短时间内的不敏感变化,可能是大多数研究尚未证明维生素D补充效果的主要原因。在这篇社论中,我们旨在讨论未来如何基于循证实践框架PICOS(参与者、干预、对照、结果和研究设计)设计维生素D治疗疾病的适当试验的观点。首先,应该选择正确的参与者,这对维生素D临床试验的成功至关重要。维生素D充足(例如,基线25(OH)D为50 nmol/L),肥胖(例如,体重指数为50 nmol/L)的参与者30 kg/m2)和/或高维生素D反应指数可排除在试验之外。其次,应使用适当形式或剂量的维生素D进行干预。建议补充适当剂量的维生素D3,使25(OH)D水平保持在75至100 nmol/L之间。第三,控制组中的“污染”需要引起注意。为了减少这种情况,理想的做法是纳入受阳光照射干扰较少的参与者(如生活在高纬度地区)或更遵守规定的参与者(较少受补充维生素d的营养素的干扰)。第四,结局指标应对变化敏感,以避免II型误差。对于骨密度、x线骨关节炎和心血管疾病等结果,可能需要随访3-5年来观察变化。最后,精确的临床试验可能是证明补充维生素D益处的唯一途径。
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
Journal of Cachexia, Sarcopenia and Muscle
Journal of Cachexia, Sarcopenia and Muscle Medicine-Orthopedics and Sports Medicine
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12.40%
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期刊介绍: The Journal of Cachexia, Sarcopenia, and Muscle is a prestigious, peer-reviewed international publication committed to disseminating research and clinical insights pertaining to cachexia, sarcopenia, body composition, and the physiological and pathophysiological alterations occurring throughout the lifespan and in various illnesses across the spectrum of life sciences. This journal serves as a valuable resource for physicians, biochemists, biologists, dieticians, pharmacologists, and students alike.
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