Relationship between Glucagon-like Peptide-1 Receptor Agonists and Cardiovascular Disease in Chronic Respiratory Disease and Diabetes

Author:

Yeh Jun-Jun1ORCID,Li Chih-Chien2,Tan Chang-Wen3,Li Chia-Hsun3,Tsai Tung-Han3,Kao Chia-Hung4567ORCID

Affiliation:

1. Department of Thoracic Medicine, Family Medicine, Geriatric Medicine and Medical Research, Ditmanson Medical Foundation, Chia-Yi Christian Hospital, Chia-Yi 600, Taiwan

2. Department of Psychotherapy, Clinical Psychology Center, Chia-Yi Christian Hospital, Chia-Yi 600, Taiwan

3. Department of Family Medicine and Medical Research, Ditmanson Medical Foundation, Chia-Yi Christian Hospital, Chia-Yi 600, Taiwan

4. Graduate Institute of Clinical Medical Science, College of Medicine, China Medical University, Taichung 404, Taiwan

5. Department of Nuclear Medicine, PET Center, China Medical University Hospital, Taichung 404, Taiwan

6. Artificial Intelligence Center, China Medical University Hospital, Taichung 404, Taiwan

7. Department of Bioinformatics and Medical Engineering, Asia University, Taichung 413, Taiwan

Abstract

The purpose of this paper is to assess the effect of glucagon-like peptide-1 receptor agonists (GLP-1RAs) on stroke or heart disease in patients having chronic respiratory disease and diabetes (CD) with underlying diseases related to COVID-19. From 1998 to 2019, we adjusted competing risk by assessing the effect of GLP-1RAs on stroke or heart disease in a CD cohort after propensity matching based on the Taiwan National Health Insurance Research Database. We also used the time-dependent method to examine the results. GLP-1 RA and non-GLP-1 RA user groups included 15,801 patients (53% women and 46% men with a mean age of 52.6 ± 12.8 years). The time between the diagnoses of DM and the initial use of the GLP-1 RA among the stroke subcohort (<2000 days) was shorter than that of the heart disease subcohort (>2000 days) (all p-values < 0.05). The overall risks of stroke, ischemic, and hemorrhagic stroke were significantly lower in GLP-1 RA users than nonusers. The adjusted subhazard ratio (aSHR) was 0.76 [95% CI 0.65–0.90], 0.77 [95% CI 0.64–0.92], and 0.69 [95% CI 0.54–0.88] (p < 0.05 for all). Furthermore, a ≥351-day use had a significantly lower stroke risk than GLP-1 RA nonusers (aSHR 0.35 [95% CI 0.26–0.49]). The time-dependent method revealed the same result, such as lower stroke, and ischemic or hemorrhagic stroke risk. In contrast, the cardiac arrhythmia incidence was higher in GLP-1 RA users with an aSHR of 1.36 [95% CI 1.16–1.59]. However, this risk disappeared after the ≥351-day use with 1.21 (0.98, 1.68) aSHR. Longer GLP-1 RA use was associated with a decreased risk of ischemic or hemorrhagic stroke and the risk of cardiac arrhythmia disappears in a CD cohort. Both a shorter lag time use of the GLP-1 RA and a longer time use of GLP-1 RA were associated with a decreased risk of ischemic or hemorrhagic stroke in the CD cohort. The GLP-1 RA use in the early stage and optimal time use in the CD cohort may avoid the stroke risk.

Funder

Taiwan Ministry of Health and Welfare Clinical Trial Center

China Medical University Hospital

Ministry of Science and Technology

Publisher

MDPI AG

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