Skip to content

Study · Not a test of the peptide alone · 2025

4 results

Factors Associated With Semaglutide Initiation Among Adults With Obesity.

Podolsky MI, Raquib R, Shafer PR, Hempstead K, Ellis RP, Stokes AC

JAMA network open2 Jan 2025Cited by 21 (Europe PMC)

Summary

ImportanceSemaglutide, a novel glucagon-like peptide-1 (GLP-1) receptor agonist medication, was approved for weight management in individuals with obesity in June 2021. There is limited evidence on factors associated with uptake among individuals in this subgroup without diabetes.ObjectiveTo explore factors associated with semaglutide initiation among a population of commercially insured individuals with obesity but no diagnosed diabetes.Design, setting, and participantsThis retrospective observational cohort study used data from the Merative MarketScan Commercial Claims and Encounters Database and included adults in the US aged 18 years or older with a first diagnosis of obesity in an outpatient or inpatient setting between June 5, 2021, and July 1, 2022. Inclusion criteria were no prior antiobesity medication, GLP-1, bariatric surgery, or diabetes-related claim in the 12 months prior to obesity diagnosis, and continuous enrollment in the 12 months preceding and 6 months following obesity diagnosis. Analysis was conducted from February to November 2024.ExposuresMedication classes prescribed, clinical diagnoses, and sociodemographic factors. Exposures were identified within the 12 months prior to obesity diagnosis.Main outcomes and measuresFactors associated with incident semaglutide prescription within 6 months after obesity diagnoses were identified using a 10-fold cross-classified random forest model. The top 20 features of the model feature importance list were ranked in a Shapley Additive Explanations plot and used in a multivariable logistic regression model to quantify associations with semaglutide initiation.ResultsIn this study of 97 456 individuals, 58 124 (59.6%) were female, 26 582 (27.3%) were aged 45 to 54 years, 50 705 (52.0%) resided in the South region, and 49 390 (50.7%) were covered by preferred provider organization plans. Of all participants, 1963 (2.0%) initiated semaglutide within 6 months of their initial obesity diagnosis. The random forest model had an area under the receiver operating characteristic curve of 0.71 (95% CI, 0.69-0.74). The most important exposures identified via Shapley Additive Explanations were sex, use of antidepressants, and employer industry. The top 20 factors were used in the logistic regression model, and significant associations were found with semaglutide initiation, including being female (adjusted odds ratio [aOR], 2.30; 95% CI, 2.05-2.58), use of certain medication classes including antidepressants (aOR,1.62; 95% CI, 1.46-1.78), and being covered by a point-of-service plan (aOR, 1.78; 95% C, 1.42-2.22).Conclusions and relevanceThis cohort study found that key sociodemographic, health care, and clinical factors are associated with receipt of semaglutide in those without diabetes. These findings suggest that insurance plan type and structure may be a crucial intervention point for improving equity in obesity treatment access.
CC BYText from Europe PMC. Highlighted sentences are the source of results.

Results from this study4

No result from this study comes from a test of the peptide.

Studies that did not test the peptide alone4

In this study, Semaglutide was a lab tool or a carrier, part of a mix, or the subject of a lab method. These results are not evidence about taking Semaglutide.

  1. 01HumanNot a test of Semaglutide aloneObservational studyOther

    Among commercially insured US adults with a first obesity diagnosis and no diabetes, 2.0% initiated semaglutide within 6 months.

    In plain wordsAmong insured US adults with obesity and no diabetes, about 2% started semaglutide within 6 months of diagnosis.

    Outcome
    Not applicableSemaglutide initiation within 6 months of obesity diagnosis
    Study

    n = 97,456

    Outcome group
    Patterns of use · Metabolic and weight

    Measurements

    Initiated semaglutide
    1963 participants
    within 6 months
    Proportion initiating
    2%
    within 6 months

    Source sentences

    Summary
    Of all participants, 1963 (2.0%) initiated semaglutide within 6 months of their initial obesity diagnosis.
    1 context sentence
    Summary · context
    To explore factors associated with semaglutide initiation among a population of commercially insured individuals with obesity but no diagnosed diabetes.

    In this study, Semaglutide was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Semaglutide.

  2. 02HumanNot a test of Semaglutide aloneObservational studyOther

    Among commercially insured US adults with obesity and no diabetes, being female was associated with higher odds of semaglutide initiation.

    In plain wordsAmong insured US adults with obesity and no diabetes, women were linked to a higher chance of starting semaglutide.

    Outcome
    Not applicableAssociation of female sex with semaglutide initiation
    Study

    n = 97,456

    Outcome group
    Patterns of use · Metabolic and weight

    Measurements

    Adjusted odds ratio
    2.3
    female

    Source sentences

    Summary
    being female (adjusted odds ratio [aOR], 2.30; 95% CI, 2.05-2.58)
    1 context sentence
    Summary · context
    To explore factors associated with semaglutide initiation among a population of commercially insured individuals with obesity but no diagnosed diabetes.

    In this study, Semaglutide was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Semaglutide.

  3. 03HumanNot a test of Semaglutide aloneObservational studyOther

    Among commercially insured US adults with obesity and no diabetes, antidepressant use was associated with higher odds of semaglutide initiation.

    In plain wordsAmong insured US adults with obesity and no diabetes, antidepressant use was linked to a higher chance of starting semaglutide.

    Outcome
    Not applicableAssociation of antidepressant use with semaglutide initiation
    Study

    n = 97,456

    Outcome group
    Patterns of use · Metabolic and weight

    Measurements

    Adjusted odds ratio
    1.62
    antidepressant use

    Source sentences

    Summary
    use of certain medication classes including antidepressants (aOR,1.62; 95% CI, 1.46-1.78)
    1 context sentence
    Summary · context
    To explore factors associated with semaglutide initiation among a population of commercially insured individuals with obesity but no diagnosed diabetes.

    In this study, Semaglutide was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Semaglutide.

  4. 04HumanNot a test of Semaglutide aloneObservational studyOther

    Among commercially insured US adults with obesity and no diabetes, point-of-service plan coverage was associated with higher odds of semaglutide initiation.

    In plain wordsAmong insured US adults with obesity and no diabetes, a point-of-service insurance plan was linked to a higher chance of starting semaglutide.

    Outcome
    Not applicableAssociation of point-of-service plan coverage with semaglutide initiation
    Study

    n = 97,456

    Outcome group
    Patterns of use · Metabolic and weight

    Measurements

    Adjusted odds ratio
    1.78
    point-of-service plan

    Source sentences

    Summary
    being covered by a point-of-service plan (aOR, 1.78; 95% C, 1.42-2.22)
    1 context sentence
    Summary · context
    To explore factors associated with semaglutide initiation among a population of commercially insured individuals with obesity but no diagnosed diabetes.

    In this study, Semaglutide was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Semaglutide.

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    11 Oct 2026, 00:04 UTC

    Study results updated

  2. Version 1

    9 Oct 2026, 03:06 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

PepBank is a research reference. Talk to a doctor before you use any peptide.