Cardiovascular safety of long-term anti-obesity drugs in subjects with overweight or obesity: a systematic review and meta-analysis

Purpose Anti-obesity therapy can reduce body weight; however, it is not clear whether it can reduce major adverse cardiovascular events (MACEs). We conducted a systematic review and meta-analysis to assess the effect of long-term anti-obesity drugs on MACEs in individuals with overweight or obesity....

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Veröffentlicht in:European journal of clinical pharmacology 2021-11, Vol.77 (11), p.1611-1621
Hauptverfasser: Zhang, Lin, Liu, Zhi, Liao, Shenling, He, He, Zhang, Mei
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container_end_page 1621
container_issue 11
container_start_page 1611
container_title European journal of clinical pharmacology
container_volume 77
creator Zhang, Lin
Liu, Zhi
Liao, Shenling
He, He
Zhang, Mei
description Purpose Anti-obesity therapy can reduce body weight; however, it is not clear whether it can reduce major adverse cardiovascular events (MACEs). We conducted a systematic review and meta-analysis to assess the effect of long-term anti-obesity drugs on MACEs in individuals with overweight or obesity. Methods The MEDLINE, Embase, and Cochrane Library databases and clinical trial registries ( https://clinicaltrials.gov ) were searched up to 3 May 2021 for randomized controlled trials (RCT) that compared anti-obesity drugs with controls and reported cardiovascular events in subjects with overweight or obesity. Heterogeneity was described by the I 2 value. The Mantel–Haenszel randomized effects model was adopted to calculate risk ratios (RR) and weighted mean differences (WMD). Sensitivity analysis was used to assess the stability of the effects. Publication bias was assessed by Begg's funnel plot and Egger's test. The Cochrane Collaboration risk-of-bias tool was used to evaluate the bias of each included RCT. Results Twelve articles were included; 21,391 and 17,618 subjects were in the anti-obesity drug and placebo groups, respectively. There was no difference in MACEs between the anti-obesity drug and placebo groups (RR 0.99; 95% CI: 0.88–1.12). Compared with placebo, anti-obesity interventions reduced body weight (WMD: − 3.96 kg; 95% CI: − 4.89, − 3.03) and improved lipid and blood glucose profiles. The intervention also did not increase the incidence of depression or anxiety or the risk of suicidal ideation. Conclusion Long-term anti-obesity drugs did not show a benefit in lowering MACEs in overweight or obese subjects, although the drugs resulted in a decrease in body weight and improved cardiometabolic parameters.
doi_str_mv 10.1007/s00228-021-03160-7
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We conducted a systematic review and meta-analysis to assess the effect of long-term anti-obesity drugs on MACEs in individuals with overweight or obesity. Methods The MEDLINE, Embase, and Cochrane Library databases and clinical trial registries ( https://clinicaltrials.gov ) were searched up to 3 May 2021 for randomized controlled trials (RCT) that compared anti-obesity drugs with controls and reported cardiovascular events in subjects with overweight or obesity. Heterogeneity was described by the I 2 value. The Mantel–Haenszel randomized effects model was adopted to calculate risk ratios (RR) and weighted mean differences (WMD). Sensitivity analysis was used to assess the stability of the effects. Publication bias was assessed by Begg's funnel plot and Egger's test. The Cochrane Collaboration risk-of-bias tool was used to evaluate the bias of each included RCT. Results Twelve articles were included; 21,391 and 17,618 subjects were in the anti-obesity drug and placebo groups, respectively. There was no difference in MACEs between the anti-obesity drug and placebo groups (RR 0.99; 95% CI: 0.88–1.12). Compared with placebo, anti-obesity interventions reduced body weight (WMD: − 3.96 kg; 95% CI: − 4.89, − 3.03) and improved lipid and blood glucose profiles. The intervention also did not increase the incidence of depression or anxiety or the risk of suicidal ideation. Conclusion Long-term anti-obesity drugs did not show a benefit in lowering MACEs in overweight or obese subjects, although the drugs resulted in a decrease in body weight and improved cardiometabolic parameters.</description><identifier>ISSN: 0031-6970</identifier><identifier>EISSN: 1432-1041</identifier><identifier>DOI: 10.1007/s00228-021-03160-7</identifier><identifier>PMID: 34043049</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Anti-Obesity Agents - administration &amp; dosage ; Anti-Obesity Agents - adverse effects ; Anti-Obesity Agents - therapeutic use ; Bias ; Biomedical and Life Sciences ; Biomedicine ; Blood Glucose - drug effects ; Body Mass Index ; Body weight ; Body Weight - drug effects ; Cardiovascular Diseases - epidemiology ; Clinical trials ; Drugs ; Humans ; Lipids - blood ; Mental Health ; Meta-analysis ; Obesity ; Obesity - drug therapy ; Obesity - epidemiology ; Overweight ; Overweight - drug therapy ; Overweight - epidemiology ; Pharmacology/Toxicology ; Placebos ; Randomized Controlled Trials as Topic ; Review ; Sensitivity analysis ; Systematic review</subject><ispartof>European journal of clinical pharmacology, 2021-11, Vol.77 (11), p.1611-1621</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2021</rights><rights>2021. 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We conducted a systematic review and meta-analysis to assess the effect of long-term anti-obesity drugs on MACEs in individuals with overweight or obesity. Methods The MEDLINE, Embase, and Cochrane Library databases and clinical trial registries ( https://clinicaltrials.gov ) were searched up to 3 May 2021 for randomized controlled trials (RCT) that compared anti-obesity drugs with controls and reported cardiovascular events in subjects with overweight or obesity. Heterogeneity was described by the I 2 value. The Mantel–Haenszel randomized effects model was adopted to calculate risk ratios (RR) and weighted mean differences (WMD). Sensitivity analysis was used to assess the stability of the effects. Publication bias was assessed by Begg's funnel plot and Egger's test. The Cochrane Collaboration risk-of-bias tool was used to evaluate the bias of each included RCT. Results Twelve articles were included; 21,391 and 17,618 subjects were in the anti-obesity drug and placebo groups, respectively. There was no difference in MACEs between the anti-obesity drug and placebo groups (RR 0.99; 95% CI: 0.88–1.12). Compared with placebo, anti-obesity interventions reduced body weight (WMD: − 3.96 kg; 95% CI: − 4.89, − 3.03) and improved lipid and blood glucose profiles. The intervention also did not increase the incidence of depression or anxiety or the risk of suicidal ideation. 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however, it is not clear whether it can reduce major adverse cardiovascular events (MACEs). We conducted a systematic review and meta-analysis to assess the effect of long-term anti-obesity drugs on MACEs in individuals with overweight or obesity. Methods The MEDLINE, Embase, and Cochrane Library databases and clinical trial registries ( https://clinicaltrials.gov ) were searched up to 3 May 2021 for randomized controlled trials (RCT) that compared anti-obesity drugs with controls and reported cardiovascular events in subjects with overweight or obesity. Heterogeneity was described by the I 2 value. The Mantel–Haenszel randomized effects model was adopted to calculate risk ratios (RR) and weighted mean differences (WMD). Sensitivity analysis was used to assess the stability of the effects. Publication bias was assessed by Begg's funnel plot and Egger's test. The Cochrane Collaboration risk-of-bias tool was used to evaluate the bias of each included RCT. Results Twelve articles were included; 21,391 and 17,618 subjects were in the anti-obesity drug and placebo groups, respectively. There was no difference in MACEs between the anti-obesity drug and placebo groups (RR 0.99; 95% CI: 0.88–1.12). Compared with placebo, anti-obesity interventions reduced body weight (WMD: − 3.96 kg; 95% CI: − 4.89, − 3.03) and improved lipid and blood glucose profiles. The intervention also did not increase the incidence of depression or anxiety or the risk of suicidal ideation. Conclusion Long-term anti-obesity drugs did not show a benefit in lowering MACEs in overweight or obese subjects, although the drugs resulted in a decrease in body weight and improved cardiometabolic parameters.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>34043049</pmid><doi>10.1007/s00228-021-03160-7</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-2076-0563</orcidid><orcidid>https://orcid.org/0000-0002-3923-3974</orcidid></addata></record>
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subjects Anti-Obesity Agents - administration & dosage
Anti-Obesity Agents - adverse effects
Anti-Obesity Agents - therapeutic use
Bias
Biomedical and Life Sciences
Biomedicine
Blood Glucose - drug effects
Body Mass Index
Body weight
Body Weight - drug effects
Cardiovascular Diseases - epidemiology
Clinical trials
Drugs
Humans
Lipids - blood
Mental Health
Meta-analysis
Obesity
Obesity - drug therapy
Obesity - epidemiology
Overweight
Overweight - drug therapy
Overweight - epidemiology
Pharmacology/Toxicology
Placebos
Randomized Controlled Trials as Topic
Review
Sensitivity analysis
Systematic review
title Cardiovascular safety of long-term anti-obesity drugs in subjects with overweight or obesity: a systematic review and meta-analysis
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