首页> 外文期刊>Journal of Clinical Movement Disorders >Characterization of vitamin D supplementation and clinical outcomes in a large cohort of early Parkinson’s disease
【24h】

Characterization of vitamin D supplementation and clinical outcomes in a large cohort of early Parkinson’s disease

机译:大量帕金森氏病早期患者的维生素D补充剂表征和临床结果

获取原文
       

摘要

Background Vitamin D (VitD) deficiency is common in Parkinson’s disease (PD) and has been raised as a possible PD risk factor. In the past decade, VitD supplementation for potential prevention of age related conditions has become more common. In this study, we sought to characterize VitD supplementation in early PD and determine as an exploratory analysis whether baseline characteristics or disease progression differed according to reported VitD use. Methods We analyzed data from the National Institutes of Health Exploratory Trials in Parkinson’s Disease (NET-PD) Long-term study (LS-1), a longitudinal study of 1741 participants. Subjects were divided into following supplement groups according to subject exposure (6?months prior to baseline and during the study): no VitD supplement, multivitamin (MVI), VitD ≥400?IU/day, and VitD + multivitamin (VitD+MVI). Clinical status was followed using the Unified Parkinson’s Disease Rating Scale, Symbol Digit Modalities Test, total daily levodopa equivalent dose, and Parkinson’s Disease Questionnaire. Results About 5% of subjects took VitD alone, 7% took VitD+MVI, 34% took MVI alone, while 54% took no supplement. Clinical outcomes at 3?years were similar across all groups. Conclusion This study shows VitD supplementation ≥400?IU/day was not common in early PD and that its use was similar to that seen in the US population. At 3?years, there was no difference in disease progression according to vitamin D supplement use.
机译:背景维生素D(VitD)缺乏症在帕金森氏病(PD)中很常见,并且已被认为是可能的PD危险因素。在过去的十年中,VitD补充剂潜在地预防了与年龄有关的疾病,这一现象变得越来越普遍。在这项研究中,我们试图对早期PD中的VitD补充进行表征,并作为探索性分析来确定基线特征或疾病进展是否根据报告的VitD使用情况而有所不同。方法我们分析了美国国立卫生研究院帕金森氏病探索性试验(NET-PD)长期研究(LS-1)的数据,该研究是一项针对1741名参与者的纵向研究。根据受试者的暴露情况(基线之前和研究期间的6个月),将受试者分为以下补充组:无VitD补充剂,多种维生素(MVI),VitD≥400?IU /天和VitD +多种维生素(VitD + MVI) 。使用统一帕金森氏病评分量表,符号数字模态测试,每日总左旋多巴当量剂量和帕金森氏病问卷对临床状况进行跟踪。结果约5%的受试者单独服用VitD,7%服用VitD + MVI,34%单独服用MVI,而54%不服用补充剂。所有组在3年时的临床结果均相似。结论这项研究表明,在PD早期,每天补充≥400?IU的VitD并不常见,其用法与美国人群相似。在3年时,根据维生素D补充剂的使用,疾病进展没有差异。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号