American journal of cardiovascular drugs : drugs, devices, and other interventions

Link between a diabetes drug and new cases of irregular heartbeat

Updated

Abstract

Out of 116,235 GLP-1RA users and 217,668 DPP4i users, the composite outcome of atrial fibrillation was similar in both groups at 4.1% for GLP-1RA and 4.3% for DPP4i.

  • No significant difference in the risk of atrial fibrillation was observed between GLP-1RA and DPP4i users, with an odds ratio of 0.96.
  • Secondary analyses indicated no differences in atrial fibrillation risk based on the duration of medication use.
  • A subgroup of individuals who achieved a 5% weight loss had a significantly lower incidence of atrial fibrillation, with an odds ratio of 0.83.
  • No significant differences in atrial fibrillation risk were noted for individuals with no weight loss or those who gained weight.

Simplified

Full Text

Full text is available at the source.

Funding

Competing interests

Declarations. Disclosures: The authors have no disclosures. Funding: No external funding was used in the preparation of this article. This material is the result of work supported with resources and the use of facilities at the Orlando VA Healthcare System (Orlando, Florida). This research was supported, in part or in whole, by HCA Healthcare and/or an HCA Healthcare affiliated entity. Conflict of interest: Suzan Khalil, William Hicks, Floyd W. Burke, and Ishak A. Mansi declare that they have no potential conflicts of interest that might be relevant to the contents of this article. Data availability statement: Data are stored in the VA Informatics and Computing Infrastructure (VINCI), the operational platform for health services research at the Veterans Healthcare Administration (VHA). VINCI acts as the data steward for VHA Data Systems. Data in VINCI cannot be copied, transferred, or printed. Access to data by other researchers is possible following VINCI protocols, as described in VINCI Central web site: http://vaww.vinci.med.va.gov/VinciCentral . Ethics approval and consent to participate: The Orlando VA institutional review board approved the study and waived participants informed consent since only preexisting deidentified data were analyzed. Code availability: Not applicable. Consent for publication: Not applicable. Author contributions: Study concept and design: IAM, SK, and FWB. Acquisition of data; statistical analysis: IAM. Interpretation of data: SK, WLH, FWB, and IAM. Drafting of the manuscript: SK and WLH. Critical revision of the manuscript for important intellectual content: IAM, FWB, and SK. Study supervision: IAM and FWB. Has full access to all the data and takes responsibility for its integrity and the data analysis: IAM.
PubMed

What Lands in Your Inbox Each Week:

  • 📚7 fresh studies
  • 📝plain-language summaries
  • direct links to original studies
  • 🏅top journal indicators
  • 📅weekly delivery
  • 🧘‍♂️always free