补充维生素D可降低糖尿病足溃疡患者的感染率并促进伤口愈合。

IF 4.6 3区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Yue-Qiao Gao, Ying-Hui Gao, Jun-Hui Xing
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引用次数: 0

摘要

背景:糖尿病足溃疡(DFUs)是一种常见且严重的糖尿病并发症,其特征是伤口愈合受损和感染风险增加。这些感染严重影响患者健康,需要广泛的医疗干预,并增加截肢的风险。维生素D (VD)在免疫调节和组织修复中起着关键作用。目的:探讨补充VD对DFUs患者感染率、伤口愈合和免疫功能的影响。方法:对120例DFUs患者进行随机对照试验。参与者被随机分配到对照组(n = 60)和干预组(n = 60),对照组接受不补充VD的标准治疗,干预组每天接受2000 IU口服VD3(胆钙化醇),持续12周。主要结局包括感染的发生率和严重程度,次要结局包括伤口愈合率、血清25-羟基维生素D水平、免疫标志物(抗菌肽、白细胞介素-6和肿瘤坏死因子-α)水平和不良事件(如高钙血症)。结果:VD补充组感染发生率(25%)明显低于对照组(45%)(P = 0.01)。在VD补充组中,需要全身抗生素或住院治疗的严重感染也较少。VD补充组伤口愈合明显增强,溃疡大小减少60%,而对照组减少35% (P < 0.01)。VD补充组血清25(OH)D水平显著升高(从16.5 ng/mL增加到35.2 ng/mL),证实了VD补充的有效性。免疫功能得到改善,如抗菌肽水平上升30%和促炎细胞因子水平下降20%所示。没有不良反应,包括高钙血症的报道。结论:补充VD可有效降低DFUs患者的感染率,促进伤口愈合,增强免疫反应。这些发现支持将VD作为一种安全有效的辅助治疗纳入dfu的临床管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Vitamin D supplementation reduces infection rate and promotes wound healing in patients with diabetic foot ulcers.

Vitamin D supplementation reduces infection rate and promotes wound healing in patients with diabetic foot ulcers.

Background: Diabetic foot ulcers (DFUs) represent a common and serious complication of diabetes, characterized by impaired wound healing and an increased risk of infection. These infections severely impact patient health, necessitating extensive medical intervention, and increasing the risk of amputation. Vitamin D (VD) plays a critical role in immune regulation and tissue repair.

Aim: To investigate the effects of VD supplementation on infection rates, wound healing, and immune function in patients with DFUs.

Methods: A randomized controlled trial was conducted involving 120 patients with DFUs. Participants were randomly assigned to either a control group (n = 60), which received standard care without VD supplementation, or an intervention group (n = 60), which received 2000 IU of oral VD3 (cholecalciferol) daily for 12 weeks. The primary outcomes included the incidence and severity of infections, whereas the secondary outcomes included wound healing rate, serum 25-hydroxyvitamin D level, levels of immune markers (cathelicidin, interleukin-6 and tumor necrosis factor-α), and adverse events, such as hypercalcemia.

Results: The incidence of infection was significantly lower in the VD supplementation group (25%) compared with the control group (45%) (P = 0.01). Severe infections requiring systemic antibiotics or hospitalization were also less frequent in the VD supplementation group. Wound healing was notably enhanced in the VD supplementation group, with a 60% reduction in ulcer size compared with a 35% reduction in the control group (P < 0.01). Serum 25(OH)D level significantly increased in the VD supplementation group (from 16.5 ng/mL to 35.2 ng/mL), confirming the efficacy of VD supplementation. Immune function improved, as demonstrated by a 30% rise in cathelicidin level and a 20% decline in levels of pro-inflammatory cytokines. No adverse effects, including hypercalcemia, were reported.

Conclusion: The VD supplementation effectively reduced infection rate, promoted wound healing, and strengthened immune responses in patients with DFUs. These findings support the incorporation of VD as a safe and effective adjunctive therapy in the clinical management of DFUs.

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来源期刊
World Journal of Diabetes
World Journal of Diabetes ENDOCRINOLOGY & METABOLISM-
自引率
2.40%
发文量
909
期刊介绍: The WJD is a high-quality, peer reviewed, open-access journal. The primary task of WJD is to rapidly publish high-quality original articles, reviews, editorials, and case reports in the field of diabetes. In order to promote productive academic communication, the peer review process for the WJD is transparent; to this end, all published manuscripts are accompanied by the anonymized reviewers’ comments as well as the authors’ responses. The primary aims of the WJD are to improve diagnostic, therapeutic and preventive modalities and the skills of clinicians and to guide clinical practice in diabetes. Scope: Diabetes Complications, Experimental Diabetes Mellitus, Type 1 Diabetes Mellitus, Type 2 Diabetes Mellitus, Diabetes, Gestational, Diabetic Angiopathies, Diabetic Cardiomyopathies, Diabetic Coma, Diabetic Ketoacidosis, Diabetic Nephropathies, Diabetic Neuropathies, Donohue Syndrome, Fetal Macrosomia, and Prediabetic State.
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