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Cardiometabolic risk factors efficacy of semaglutide in the STEP program.

Postgraduate medicine
January 1, 2022
Anastassia Amaro et al. (3 authors)
Clinical Trial, Phase IIIJournal ArticleHuman StudyClinical
Study Details

Study Goal

The researchers aimed to compare the efficacy of once-weekly subcutaneous semaglutide 2.4 mg versus placebo for weight loss and improvements in cardiometabolic parameters in people with obesity.

Results Summary

Semaglutide led to greater reductions in body weight, waist circumference, BMI, systolic and diastolic blood pressure, and positive changes in HbA1c compared to placebo across multiple trials.

Population

People with overweight or obesity.

Effective Dosage

Once-weekly subcutaneous semaglutide 2.4 mg.

Duration

Not specified in the abstract.

Interactions

None mentioned.

Extracted Claims (6)
InterventionDirectionEndpointPopulationDosageImpactClaim #
once-weekly subcutaneous semaglutide 2.4 mg
decrease
body weight
people with obesity
-
greater reductions from baseline versus placebo
#1
once-weekly subcutaneous semaglutide 2.4 mg
decrease
waist circumference
people with obesity
-
greater reductions from baseline versus placebo
#2
once-weekly subcutaneous semaglutide 2.4 mg
decrease
body mass index
people with obesity
-
greater reductions from baseline versus placebo
#3
once-weekly subcutaneous semaglutide 2.4 mg
decrease
systolic blood pressure (SBP)
people with obesity
-
greater reductions from baseline versus placebo
#4
once-weekly subcutaneous semaglutide 2.4 mg
decrease
diastolic blood pressure
people with obesity
-
greater reductions from baseline versus placebo
#5
once-weekly subcutaneous semaglutide 2.4 mg
decrease
glycated hemoglobin (HbA1c)
people with obesity
-
positive changes
#6
Abstract

People with overweight or obesity often suffer from associated cardiometabolic diseases and comorbidities. Current therapies for obesity include lifestyle intervention, bariatric surgery, and pharmacotherapy. The magnitude of weight loss achieved with these therapies can determine the level of improvement in various comorbidities. Once-weekly subcutaneous semaglutide 2.4 mg is a glucagon-like peptide-1 receptor agonist recently approved by the US Food and Drug Administration for the treatment of obesity. This article reviews data from the global phase 3 Semaglutide Treatment Effect in People with obesity (STEP) program, comparing the efficacy of once-weekly subcutaneous semaglutide 2.4 mg versus placebo for weight loss and improvements in cardiometabolic parameters across the STEP 1 to 5 trials. In STEP 1 to 3 and STEP 5, semaglutide led to greater reductions from baseline versus placebo in body weight, waist circumference, body mass index, systolic blood pressure (SBP), and diastolic blood pressure, as well as positive changes in glycated hemoglobin (HbA

Medical Subject Headings (MeSH)
HumansCardiometabolic Risk FactorsCardiovascular DiseasesDiabetes Mellitus, Type 2Glucagon-Like PeptidesHypoglycemic AgentsLipidsObesityOverweightWeight Loss
Study Links
Quality Scores
SafetyNot Assessed
Efficacy85/10
Quality90/10
Citation Metrics
Total Citations3
Citations/Year1.0
Relative Citation Ratio0.28
NIH Percentile14.9%
Research Impact Scores
APT Score0.25
Weight Score2.61
Normalized Score0.72
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