PMID- 37964480 OWN - NLM STAT- MEDLINE DCOM- 20240125 LR - 20240417 IS - 1752-8062 (Electronic) IS - 1752-8054 (Print) IS - 1752-8054 (Linking) VI - 17 IP - 1 DP - 2024 Jan TI - Risk factors for hyperglycemia in COVID-19 patients treated with remdesivir. PG - e13684 LID - 10.1111/cts.13684 [doi] LID - e13684 AB - The primary objective of this study was to investigate the factors contributing to hyperglycemic adverse events (AEs) associated with the administration of remdesivir in hospitalized patients diagnosed with coronavirus disease 2019 (COVID-19). Furthermore, the study aimed to develop a risk score model employing various machine learning approaches. A total of 1262 patients were enrolled in this investigation. The relationship between covariates and hyperglycemic AEs was assessed through logistic regression analysis. Diverse machine learning algorithms were employed for the purpose of forecasting hyperglycemia-related complications. After adjusting for covariates, individuals with a body mass index >/=23 kg/m(2) , those using proton pump inhibitors, cholinergic medications, or individuals with cardiovascular diseases exhibited approximately 2.41-, 2.73-, 2.65-, and 1.97-fold higher risks of experiencing hyperglycemic AEs (95% CI 1.271-4.577, 1.223-6.081, 1.168-5.989, and 1.119-3.472, respectively). Multivariate logistic regression, elastic net, and random forest models displayed area under the receiver operating characteristic curve values of 0.65, 0.66, and 0.60, respectively (95% CI 0.572-0.719, 0.640-0.671, and 0.583-0.611, respectively). This study comprehensively explored factors associated with hyperglycemic complications arising from remdesivir administration and, concurrently, leveraged a range of machine learning methodologies to construct a risk scoring model, thereby facilitating the tailoring of individualized remdesivir treatment regimens for patients with COVID-19. CI - (c) 2023 The Authors. Clinical and Translational Science published by Wiley Periodicals LLC on behalf of American Society for Clinical Pharmacology and Therapeutics. FAU - Kim, Woorim AU - Kim W AD - College of Pharmacy, Chungbuk National University, Cheongju-si, Korea. AD - Department of Pharmacy, Kangwon National University, Chuncheon, Korea. FAU - Lee, Go Woon AU - Lee GW AD - College of Pharmacy, Chungbuk National University, Cheongju-si, Korea. AD - Department of Pharmacy, Bestian Hospital, Cheongju-si, Korea. FAU - Rhee, Nuga AU - Rhee N AD - Medical Department, Bestian Hospital, Cheongju-si, Korea. FAU - Min, Kyung Hyun AU - Min KH AD - College of Pharmacy, Chungbuk National University, Cheongju-si, Korea. FAU - Kim, Jun Hyeob AU - Kim JH AD - College of Pharmacy, Chungbuk National University, Cheongju-si, Korea. FAU - Gil, Jin Yeon AU - Gil JY AD - College of Pharmacy, Chungbuk National University, Cheongju-si, Korea. FAU - Kim, Song Yi AU - Kim SY AD - College of Pharmacy, Chungbuk National University, Cheongju-si, Korea. AD - National Institute of Food and Drug Safety Evaluation, Cheongju-si, Korea. FAU - Han, Ji Min AU - Han JM AD - College of Pharmacy, Chungbuk National University, Cheongju-si, Korea. FAU - Lee, Kyung Eun AU - Lee KE AD - College of Pharmacy, Chungbuk National University, Cheongju-si, Korea. LA - eng GR - 2021RIS-001/Regional Innovation Strategy/ GR - 2017R1A5A2015541/Medical Research Center Program/ GR - National Research Foundation funded by the Korean Government Ministry of Education and Ministry of Science and Information and Communication Technology (ICT)/ PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20231128 PL - United States TA - Clin Transl Sci JT - Clinical and translational science JID - 101474067 RN - 3QKI37EEHE (remdesivir) RN - 415SHH325A (Adenosine Monophosphate) RN - OF5P57N2ZX (Alanine) SB - IM MH - Humans MH - *COVID-19 MH - COVID-19 Drug Treatment MH - Risk Factors MH - *Hyperglycemia MH - Adenosine Monophosphate/*analogs & derivatives MH - Alanine/*analogs & derivatives PMC - PMC10766056 COIS- All the authors have declared that they have no competing interests. EDAT- 2023/11/15 06:42 MHDA- 2024/01/25 06:43 PMCR- 2023/11/28 CRDT- 2023/11/15 00:33 PHST- 2023/09/26 00:00 [revised] PHST- 2023/06/29 00:00 [received] PHST- 2023/10/28 00:00 [accepted] PHST- 2024/01/25 06:43 [medline] PHST- 2023/11/15 06:42 [pubmed] PHST- 2023/11/15 00:33 [entrez] PHST- 2023/11/28 00:00 [pmc-release] AID - CTS13684 [pii] AID - 10.1111/cts.13684 [doi] PST - ppublish SO - Clin Transl Sci. 2024 Jan;17(1):e13684. doi: 10.1111/cts.13684. Epub 2023 Nov 28.