Association between ICS use and risk of hyperglycemia in COPD patients: systematic review and meta-analysis
Abstract Background The effect of inhaled corticosteroids (ICS) on risk of hyperglycemia in patients with chronic obstructive pulmonary disease (COPD) remains ambiguous. The aim of this study is to evaluate the association between ICS use and the incidence of hyperglycemia related adverse effects in...
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doaj-8bd3c4fd9b8f40f989311579a50d02bf2021-07-11T11:39:35ZengBMCRespiratory Research1465-993X2021-07-0122111010.1186/s12931-021-01789-7Association between ICS use and risk of hyperglycemia in COPD patients: systematic review and meta-analysisXiaofeng Pu0Liang Liu1Bimin Feng2Zhengji Zhang3Guojun Wang4Department of Pharmacy, The Affiliated Hospital of Southwest Medical UniversityDepartment of Clinical Pharmacy, School of Pharmacy, Southwest Medical UniversityDepartment of Clinical Pharmacy, School of Pharmacy, Southwest Medical UniversityDepartment of Pharmacy, The Affiliated Hospital of Southwest Medical UniversityDepartment of Pharmacy, The Affiliated Hospital of Southwest Medical UniversityAbstract Background The effect of inhaled corticosteroids (ICS) on risk of hyperglycemia in patients with chronic obstructive pulmonary disease (COPD) remains ambiguous. The aim of this study is to evaluate the association between ICS use and the incidence of hyperglycemia related adverse effects in COPD patients. Methods Medline/PubMed, Embase, the Cochrane Central Register of Controlled Trials (CENTRAL), and ClinicalTrials.gov were searched from inception to 25 May 2020. Randomized controlled trials (RCTs) of ICS versus control (non-ICS) treatment for COPD patients reporting on risk of hyperglycemia were included. The Mantel–Haenszel method with fixed-effects modeling was used to calculate pooled relative risks (RRs) and 95% confidence intervals (CIs). Results Seventeen RCTs with 43,430 subjects were included in the meta-analysis. Pooled results suggested that there was no statistically significant difference in the risk of hyperglycemia between the ICS group and the control group (RR 1.02, 95% CI 0.90–1.16, P = 0.76). In addition, no significant difference was noted in the effect on glucose level (RR 1.20, 95% CI 0.79–1.82, P = 0.40), risk of diabetes progression (RR 0.84, 95% CI 0.20–3.51, P = 0.81) and new onset diabetes mellitus (RR 1.0, 95% CI 0.88–1.15, P = 0.95) between the ICS group and the control group. These findings also were consistent across all subgroup analyses. Conclusions Use of ICS does not have an effect on the blood glucose and is not associated with the risk of new onset diabetes mellitus and diabetes progression in patients with COPD. Further RCTs exploring the association between ICS use and risk of hyperglycemia in COPD patients are still needed to verify our results of this analysis.https://doi.org/10.1186/s12931-021-01789-7COPDInhaled corticosteroidsRandomised controlled trialsMeta-analysis |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Xiaofeng Pu Liang Liu Bimin Feng Zhengji Zhang Guojun Wang |
spellingShingle |
Xiaofeng Pu Liang Liu Bimin Feng Zhengji Zhang Guojun Wang Association between ICS use and risk of hyperglycemia in COPD patients: systematic review and meta-analysis Respiratory Research COPD Inhaled corticosteroids Randomised controlled trials Meta-analysis |
author_facet |
Xiaofeng Pu Liang Liu Bimin Feng Zhengji Zhang Guojun Wang |
author_sort |
Xiaofeng Pu |
title |
Association between ICS use and risk of hyperglycemia in COPD patients: systematic review and meta-analysis |
title_short |
Association between ICS use and risk of hyperglycemia in COPD patients: systematic review and meta-analysis |
title_full |
Association between ICS use and risk of hyperglycemia in COPD patients: systematic review and meta-analysis |
title_fullStr |
Association between ICS use and risk of hyperglycemia in COPD patients: systematic review and meta-analysis |
title_full_unstemmed |
Association between ICS use and risk of hyperglycemia in COPD patients: systematic review and meta-analysis |
title_sort |
association between ics use and risk of hyperglycemia in copd patients: systematic review and meta-analysis |
publisher |
BMC |
series |
Respiratory Research |
issn |
1465-993X |
publishDate |
2021-07-01 |
description |
Abstract Background The effect of inhaled corticosteroids (ICS) on risk of hyperglycemia in patients with chronic obstructive pulmonary disease (COPD) remains ambiguous. The aim of this study is to evaluate the association between ICS use and the incidence of hyperglycemia related adverse effects in COPD patients. Methods Medline/PubMed, Embase, the Cochrane Central Register of Controlled Trials (CENTRAL), and ClinicalTrials.gov were searched from inception to 25 May 2020. Randomized controlled trials (RCTs) of ICS versus control (non-ICS) treatment for COPD patients reporting on risk of hyperglycemia were included. The Mantel–Haenszel method with fixed-effects modeling was used to calculate pooled relative risks (RRs) and 95% confidence intervals (CIs). Results Seventeen RCTs with 43,430 subjects were included in the meta-analysis. Pooled results suggested that there was no statistically significant difference in the risk of hyperglycemia between the ICS group and the control group (RR 1.02, 95% CI 0.90–1.16, P = 0.76). In addition, no significant difference was noted in the effect on glucose level (RR 1.20, 95% CI 0.79–1.82, P = 0.40), risk of diabetes progression (RR 0.84, 95% CI 0.20–3.51, P = 0.81) and new onset diabetes mellitus (RR 1.0, 95% CI 0.88–1.15, P = 0.95) between the ICS group and the control group. These findings also were consistent across all subgroup analyses. Conclusions Use of ICS does not have an effect on the blood glucose and is not associated with the risk of new onset diabetes mellitus and diabetes progression in patients with COPD. Further RCTs exploring the association between ICS use and risk of hyperglycemia in COPD patients are still needed to verify our results of this analysis. |
topic |
COPD Inhaled corticosteroids Randomised controlled trials Meta-analysis |
url |
https://doi.org/10.1186/s12931-021-01789-7 |
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