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维生素 D 补充对肥胖或超重个体中心血液动力学参数和自主神经系统的影响。

Effects of Vitamin D Supplementation on Central Hemodynamic Parameters and Autonomic Nervous System in Obese or Overweight Individuals.

机构信息

Departamento de Clínica Médica, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ - Brasil.

Departamento de Nutrição Aplicada, Instituto de Nutrição, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ - Brasil.

出版信息

Arq Bras Cardiol. 2024 Apr;121(5):e20230678. doi: 10.36660/abc.20230678.

DOI:10.36660/abc.20230678
PMID:38747749
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11098585/
Abstract

BACKGROUND

Previous studies have been inconsistent in demonstrating beneficial cardiovascular effects of vitamin D supplementation.

OBJECTIVE

To evaluate the effects of vitamin D3 supplementation on central hemodynamic parameters and autonomic activity in obese/overweight individuals with low vitamin D levels (<30ng/dl).

METHODS

Adults 40-65 years old with body mass index ≥25<40 kg/m2 were enrolled in this prospective, randomized, double-blind clinical trial (NCT05689632). Central hemodynamics was assessed using the oscillometric method (Mobil-O-Graph®), and heart rate variability using a Polar heart rate monitor (Kubios® software). Patients (n=53) received a placebo in the control group (CO, n=25) or vitamin D3 (VD, n=28) 7000 IU/day, and were evaluated before (W0) and after 8 weeks (W8) with a significance level of 0.05.

RESULTS

The groups were homogeneous regarding age (51±6 vs 52±6 years, p=0.509) and vitamin D levels (22.8±4.9 vs 21.7±4.5ng/ml, p=0.590). At W8, the VD group had significantly higher levels of vitamin D (22.5 vs 35.6ng/ml, p<0.001). Only the VD group showed a significant reduction in systolic blood pressure (SBP; 123±15 vs 119±14mmHg, p=0.019) and alkaline phosphatase (213±55 vs 202±55mg/dl, p=0.012). The CO group showed an increase in augmentation pressure (AP: 9 vs 12 mmHg, p=0.028) and augmentation index (AIx: 26 vs 35%, p=0.020), which was not observed in the VD group (AP: 8 vs 8 mmHg, AIx: 26 vs 25%, p>0.05). VD group showed an increase in the parasympathetic nervous system index (PNSi) (-0.64±0.94 vs -0.16±1.10, p=0.028) and the R-R interval (866±138 vs 924±161 ms, p= 0.026).

CONCLUSION

In this sample, eight weeks of daily vitamin D supplementation resulted in an improvement in blood pressure levels and autonomic balance.

摘要

背景

先前的研究结果并不一致,无法明确维生素 D 补充对心血管的有益作用。

目的

评估维生素 D3 补充对维生素 D 水平较低(<30ng/dl)的肥胖/超重个体中心血管参数和自主活动的影响。

方法

本前瞻性、随机、双盲临床试验(NCT05689632)纳入 40-65 岁、BMI≥25<40kg/m2 的成年人。采用振荡法(Mobil-O-Graph®)评估中心血管动力学,使用 Polar 心率监测仪(Kubios®软件)评估心率变异性。患者(n=53)被随机分为对照组(CO,n=25)或维生素 D3 组(VD,n=28),每天服用 7000IU 维生素 D3。在 8 周(W8)时进行评估,以 0.05 为显著性水平。

结果

两组年龄(51±6 岁 vs 52±6 岁,p=0.509)和维生素 D 水平(22.8±4.9ng/ml vs 21.7±4.5ng/ml,p=0.590)具有同质性。在 W8 时,VD 组的维生素 D 水平显著升高(22.5ng/ml vs 35.6ng/ml,p<0.001)。仅 VD 组的收缩压(SBP;123±15mmHg vs 119±14mmHg,p=0.019)和碱性磷酸酶(213±55mg/dl vs 202±55mg/dl,p=0.012)显著降低。CO 组的增强压(AP;9mmHg vs 12mmHg,p=0.028)和增强指数(AIx;26% vs 35%,p=0.020)增加,而 VD 组未观察到这一变化(AP;8mmHg vs 8mmHg,AIx;26% vs 25%,p>0.05)。VD 组副交感神经指数(PNSi;-0.64±0.94 比 -0.16±1.10,p=0.028)和 R-R 间期(866±138ms vs 924±161ms,p=0.026)增加。

结论

在本样本中,每日补充 8 周维生素 D 可改善血压水平和自主平衡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d810/11098585/1d828ef80766/0066-782X-abc-121-5-e20230678-gf04-en.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d810/11098585/d5ac15fb8311/0066-782X-abc-121-5-e20230678-gf01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d810/11098585/24512a833786/0066-782X-abc-121-5-e20230678-gf02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d810/11098585/0d32afa40103/0066-782X-abc-121-5-e20230678-gf03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d810/11098585/7ac7ed54135f/0066-782X-abc-121-5-e20230678-gf04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d810/11098585/dc99df24ec8b/0066-782X-abc-121-5-e20230678-gf01-en.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d810/11098585/40576a102f7d/0066-782X-abc-121-5-e20230678-gf02-en.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d810/11098585/fff0995f7c38/0066-782X-abc-121-5-e20230678-gf03-en.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d810/11098585/1d828ef80766/0066-782X-abc-121-5-e20230678-gf04-en.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d810/11098585/d5ac15fb8311/0066-782X-abc-121-5-e20230678-gf01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d810/11098585/24512a833786/0066-782X-abc-121-5-e20230678-gf02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d810/11098585/0d32afa40103/0066-782X-abc-121-5-e20230678-gf03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d810/11098585/7ac7ed54135f/0066-782X-abc-121-5-e20230678-gf04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d810/11098585/dc99df24ec8b/0066-782X-abc-121-5-e20230678-gf01-en.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d810/11098585/40576a102f7d/0066-782X-abc-121-5-e20230678-gf02-en.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d810/11098585/fff0995f7c38/0066-782X-abc-121-5-e20230678-gf03-en.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d810/11098585/1d828ef80766/0066-782X-abc-121-5-e20230678-gf04-en.jpg

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