PMID- 37431351 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20231102 IS - 2168-8184 (Print) IS - 2168-8184 (Electronic) IS - 2168-8184 (Linking) VI - 15 IP - 6 DP - 2023 Jun TI - Glycemic Control and the Weight Benefit of a Daily 7 mg Dose of Oral Semaglutide Versus an Alternate-Day 14 mg Dose of Oral Semaglutide From an Ambulatory Glucose Monitoring Data: A Retrospective Cohort Study From Eastern India. PG - e40179 LID - 10.7759/cureus.40179 [doi] LID - e40179 AB - INTRODUCTION: Oral semaglutide is a glucagon-like peptide-1 receptor agonist (GLP-1RA) class of antidiabetic medication. High costs and GI side effects are the major limitations of its widespread use. Some patients who were on a 14 mg dose of oral semaglutide self-prescribed an alternate-day schedule to mitigate GI side effects and to reduce the cost. METHODS: This retrospective observational cohort study evaluates the ambulatory glucose profile (AGP) data, extrapolated glycosylated hemoglobin (HbA1C), and BMI of 11 types of 2 diabetes mellitus (T2DM) while they were on an alternate-day 14 mg dose of oral semaglutide compared to their record while on a daily 7 mg dose. The AGP metrics (time-in-range (TIR), time-below-range (TBR), and time-above-range (TAR)) along with extrapolated HbA1C and BMI were analyzed. Statistical analysis was done using SPSS Statistics version 21.0. RESULTS: No statistically significant difference in the AGP metrics between the AGP profile of a daily 7 mg dose and the AGP profile of an alternate-day 14 mg dose of oral semaglutide was observed. Interestingly, a statistically significant progressive decline in BMI value was observed even on the alternate-day 14 mg dose when compared to the daily 7 mg dose. CONCLUSION: In this small cohort of patients, the metrics of short-term glycemic control and the extrapolated HbA1C values were similar for the daily 7 mg dose versus the alternate-day 14 mg dose of oral semaglutide. BMI showed progressive reduction which was statistically significant even with the alternate-day 14 mg dose of oral semaglutide. CI - Copyright (c) 2023, RoyChaudhuri et al. FAU - RoyChaudhuri, Soumyabrata AU - RoyChaudhuri S AD - Diabetes and Endocrinology, Kali Prasad Chowdhury Medical College and Hospital, Kolkata, IND. FAU - Majumder, Anirban AU - Majumder A AD - Diabetes and Endocrinology, Kali Prasad Chowdhury Medical College and Hospital, Kolkata, IND. FAU - Mukherjee, Poulomi AU - Mukherjee P AD - Community Medicine, Medical College and Hospital, Kolkata, IND. FAU - Sanyal, Debmalya AU - Sanyal D AD - Diabetes and Endocrinology, Kali Prasad Chowdhury Medical College and Hospital, Kolkata, IND. FAU - Chakraborty, Soma AU - Chakraborty S AD - Diabetes and Endocrinology, Diabetes-Obesity-Thyroid-Hormone Clinic, Kolkata, IND. FAU - Chuyan, Susama AU - Chuyan S AD - Diabetes and Endocrinology, Adopt Endocrine, Kolkata, IND. LA - eng PT - Journal Article DEP - 20230609 PL - United States TA - Cureus JT - Cureus JID - 101596737 PMC - PMC10329815 OTO - NOTNLM OT - ambulatory glucose profile (agp) OT - body mass index (bmi) OT - glycaemic control OT - oral semaglutide OT - types 2 diabetes COIS- The authors have declared financial relationships, which are detailed in the next section. EDAT- 2023/07/11 06:42 MHDA- 2023/07/11 06:43 PMCR- 2023/06/09 CRDT- 2023/07/11 03:35 PHST- 2023/06/09 00:00 [accepted] PHST- 2023/07/11 06:43 [medline] PHST- 2023/07/11 06:42 [pubmed] PHST- 2023/07/11 03:35 [entrez] PHST- 2023/06/09 00:00 [pmc-release] AID - 10.7759/cureus.40179 [doi] PST - epublish SO - Cureus. 2023 Jun 9;15(6):e40179. doi: 10.7759/cureus.40179. eCollection 2023 Jun.