Serum 25-hydroxyvitamin D concentrations and their impact on all-cause mortality in Parkinson’s disease: insights from National Health and Nutrition Examination Survey 1999–2020 data

Yufei Yong, Hui Dong, Zhen Zhou, Yan Zhu, Meiling Gu, Wenxiao Li
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Abstract

This study explores the relationship between serum 25-hydroxyvitamin D [25(OH)D] levels and mortality among Parkinson’s disease (PD) patients, providing evidence for the potential benefits of vitamin D (VD) supplementation.PD patients were collected from the National Health and Nutrition Examination Survey (NHANES) database from 1999 to 2020. These patients were categorized based on their serum 25(OH)D levels: deficiency, insufficiency, and sufficiency. We compared demographic information and analyzed mortality data from the National Death Index. A restricted cubic spline model assessed the nonlinear association between 25(OH)D levels and mortality, complemented by multivariable Cox regression analysis. Consistency of results was checked through subgroup analysis.The study included 364 PD patients: 87 (23.9%) with VD deficiency, 121 (33.2%) with insufficiency, and 156 (42.9%) with sufficiency. Demographically, 46.4% were male, and 56% were over 65 years. The deficiency group predominantly consisted of Mexican Americans (53.1%), had lower income levels, a higher unmarried rate, and increased liver disease incidence. The analysis showed a U-shaped curve between 25(OH)D levels and mortality risk, with the lowest risk at 78.68 nmol/L (p-non-linear = 0.007, p-overall = 0.008). Kaplan–Meier analysis found the highest survival rates in patients with 25(OH)D levels between 75–100 nmol/L (p = 0.039). Compared to this group, patients with levels below 50 nmol/L had a 3.52-fold increased mortality risk (95% CI = 1.58–7.86, p = 0.002), and those above 100 nmol/L had a 2.92-fold increase (95% CI = 1.06–8.05, p = 0.038). Age-specific subgroup analysis (p = 0.009) revealed that both very low (<50 nmol/L) and high (>100 nmol/L) levels increased mortality risk in patients under 65, while levels below 75 nmol/L raised mortality risk in older patients.Serum 25(OH)D levels are nonlinearly linked to mortality in PD patients, with optimal survival rates occurring at 75–100 nmol/L. Deviations from this range increase the risk of death.
血清 25-羟基维生素 D 浓度及其对帕金森病全因死亡率的影响:从 1999-2020 年全国健康与营养调查数据中获得的启示
本研究探讨了帕金森病(PD)患者血清25-羟基维生素D [25(OH)D]水平与死亡率之间的关系,为补充维生素D(VD)的潜在益处提供了证据。帕金森病患者是从1999年至2020年美国国家健康与营养调查(NHANES)数据库中收集的。这些患者根据其血清 25(OH)D 水平分为:缺乏、不足和充足。我们比较了人口统计学信息,并分析了国家死亡指数中的死亡率数据。限制性三次样条模型评估了 25(OH)D 水平与死亡率之间的非线性关系,并辅以多变量 Cox 回归分析。研究纳入了 364 名帕金森病患者:研究共纳入 364 名帕金森病患者:87 人(23.9%)VD 缺乏,121 人(33.2%)VD 不足,156 人(42.9%)VD 充足。从人口统计学角度看,46.4%的患者为男性,56%的患者年龄在65岁以上。缺乏症组主要由墨西哥裔美国人(53.1%)组成,收入水平较低,未婚率较高,肝病发病率较高。分析结果显示,25(OH)D水平与死亡风险之间呈U形曲线,78.68 nmol/L时风险最低(p-非线性=0.007,p-总体=0.008)。卡普兰-梅耶尔分析发现,25(OH)D 水平在 75-100 毫摩尔/升之间的患者生存率最高(p = 0.039)。与该组患者相比,水平低于 50 nmol/L 的患者的死亡风险增加了 3.52 倍(95% CI = 1.58-7.86,p = 0.002),高于 100 nmol/L 的患者的死亡风险增加了 2.92 倍(95% CI = 1.06-8.05,p = 0.038)。年龄特异性亚组分析(p = 0.009)显示,极低(100 nmol/L)的水平会增加 65 岁以下患者的死亡风险,而低于 75 nmol/L 的水平会增加老年患者的死亡风险。偏离这一范围会增加死亡风险。
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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