Effects of Vitamin D on Respiratory Function and Immune Status for Patients with Chronic Obstructive Pulmonary Disease (COPD): A Systematic Review and Meta-Analysis
Huan Yang, Deyang Sun, Fengqing Wu, Xiao Xu, Xi Liu, Zhen Wang, Linshui Zhou
Abstract
Background. Many studies have demonstrated that vitamin D has clinical benefits when used to treat patients with chronic obstructive pulmonary disease (COPD). However, most of these studies have insufficient samples or inconsistent results. The aim of this meta-analysis was to evaluate the effects of vitamin D therapy in patients with COPD. Methods. We performed a comprehensive retrieval in the following electronic databases: PubMed, Embase, Cochrane Library, China National Knowledge Infrastructure (CNKI), Wanfang Data, and Chinese Scientific Journals Database (VIP). Two trained reviewers identified relevant studies, extracted data information, and then assessed the methodical quality by the Cochrane risk of bias assessment tool, independently. Then, the meta-analyses were conducted by RevMan 5.4, binary variables were represented by risks ratio (RR), and continuous variables were represented by mean difference (MD) or standardized mean difference (SMD) to assess the efficacy of vitamin D therapy in patients with COPD. Then, publication bias assessment was conducted by funnel plot analysis. Finally, the quality of evidence was assessed by the GRADE system. Results. A total of 15 articles involving 1598 participants were included in this study. The overall results showed a statistical significance of vitamin D therapy in patients with COPD which can significantly improve forced expiratory volume in 1 second (FEV1) (MD: 5.69, 95% CI: 5.01-6.38, <a:math xmlns:a="http://www.w3.org/1998/Math/MathML" id="M1"> <a:mi>P</a:mi> <a:mo><</a:mo> <a:mn>0.00001</a:mn> </a:math> , <c:math xmlns:c="http://www.w3.org/1998/Math/MathML" id="M2"> <c:mtext>I</c:mtext> <c:mn>2</c:mn> <c:mo>=</c:mo> <c:mn>51</c:mn> <c:mi>%</c:mi> </c:math> ) and FEV1/FVC (SMD:0.49, 95% CI: 0.39-0.60, <e:math xmlns:e="http://www.w3.org/1998/Math/MathML" id="M3"> <e:mi>P</e:mi> <e:mo><</e:mo> <e:mn>0.00001</e:mn> </e:math> , <g:math xmlns:g="http://www.w3.org/1998/Math/MathML" id="M4"> <g:mtext>I</g:mtext> <g:mn>2</g:mn> <g:mo>=</g:mo> <g:mn>84</g:mn> <g:mi>%</g:mi> </g:math> ); and serum 25 (OH)D (SMD:1.21, 95% CI:1.07-1.34, <i:math xmlns:i="http://www.w3.org/1998/Math/MathML" id="M5"> <i:mi>P</i:mi> <i:mo><</i:mo> <i:mn>0.00001</i:mn> </i:math> , <k:math xmlns:k="http://www.w3.org/1998/Math/MathML" id="M6"> <k:mtext>I</k:mtext> <k:mn>2</k:mn> <k:mo>=</k:mo> <k:mn>98</k:mn> <k:mi>%</k:mi> </k:math> ) also increase CD3+ Tcells (MD: 6.67, 95% CI: 5.34-8.00, <m:math xmlns:m="http://www.w3.org/1998/Math/MathML" id="M7"> <m:mi>P</m:mi> <m:mo><</m:mo> <m:mn>0.00001</m:mn> </m:math> , <o:math xmlns:o="http://www.w3.org/1998/Math/MathML" id="M8"> <o:mtext>I</o:mtext> <o:mn>2</o:mn> <o:mo>=</o:mo> <o:mn>78</o:mn> <o:mi>%</o:mi> </o:math> ) and CD4+ T cells (MD: 6.00, 95% CI: 5.01-7.00, <q:math xmlns:q="http://www.w3.org/1998/Math/MathML" id="M9"> <q:mi>P</q:mi> <q:mo><</q:mo> <q:mn>0.00001</q:mn> </q:math> , <s:math xmlns:s="http://www.w3.org/1998/Math/MathML" id="M10"> <s:mtext>I</s:mtext> <s:mn>2</s:mn> <s:mo>=</s:mo> <s:mn>65</s:mn> <s:mi>%</s:mi> </s:math> ); and T lymphocyte CD4+/CD8+ ratio (MD: 0.41, 95% CI: 0.20-0.61, <u:math xmlns:u="http://www.w3.org/1998/Math/MathML" id="M11"> <u:mi>P</u:mi> <u:mo>=</u:mo> <u:mn>0.0001</u:mn> </u:math> , <w:math xmlns:w="http://www.w3.org/1998/Math/MathML" id="M12"> <w:mtext>I</w:mtext> <w:mn>2</w:mn> <w:mo>=</w:mo> <w:mn>95</w:mn> <w:mi>%</w:mi> </w:math> ) obviously decrease CD8+ Tcells(SMD: -0.83, 95% CI: -1.05- -0.06, <y:math xmlns:y="http://www.w3.org/1998/Math/MathML" id="M13"> <y:mi>P</y:mi> <y:mo><</y:mo> <y:mn>0.00001</y:mn> </y:math> , <ab:math xmlns:ab="http://www.w3.org/1998/Math/MathML" id="M14"> <ab:mtext>I</ab:mtext> <ab:mn>2</ab:mn> <ab:mo>=</ab:mo> <ab:mn>82</ab:mn> <ab:mi>%</ab:mi> </ab:math> ), the times of acute exacerbation (RR: 0.40, 95% CI: 0.28-0.59, <cb:math xmlns:cb="http://www.w3.org/1998/Math/MathML" id="M15"> <cb:mi>P</cb:mi> <cb:mo><</cb:mo> <cb:mn>0.00001</cb:mn> </cb:math> , <eb:math xmlns:eb="http://www.w3.org/1998/Math/MathML" id="M16"> <eb:mtext>I</eb:mtext> <eb:mn>2</eb:mn> <eb:mo>=</eb:mo> <eb:mn>0</eb:mn> <eb:mi>%</eb:mi> </eb:math> ), and COPD assessment test (CAT) score (MD: -3.77, 95% CI: -5.86 - -1.68, <gb:math xmlns:gb="http://www.w3.org/1998/Math/MathML" id="M17"> <gb:mi>P</gb:mi> <gb:mo>=</gb:mo> <gb:mn>0.0004</gb:mn> </gb:math> , <ib:math xmlns:ib="http://www.w3.org/1998/Math/MathML" id="M18"> <ib:mtext>I</ib:mtext> <ib:mn>2</ib:mn> <ib:mo>=</ib:mo> <ib:mn>79</ib:mn> <ib:mi>%</ib:mi> </ib:math> ). Conclusions. Our analysis indicated that vitamin D used in patients with COPD could improve the lung function (FEV1 and FEV1/FVC), the serum 25(OH)D, CD3+ T cells, CD4 + T cells, and T lymphocyte CD4+/CD8+ ratio and reduce CD8+ T cells, acute exacerbation, and CAT scores.