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Blood glucose levels and bodyweight change after dapagliflozin administration

AIMS/INTRODUCTION: Increased blood glucose or increased weight is often observed in patients who are prescribed sodium–glucose cotransporter 2 inhibitors (SGLT2i). The aim of this study was to determine in advance which patients, among those prescribed a SGLT2i, would be likely to have improved or w...

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Autores principales: Kim, Hyunah, Lee, Seung‐Hwan, Lee, Hyunyong, Yim, Hyeon Woo, Cho, Jae‐Hyoung, Yoon, Kun‐Ho, Kim, Hun‐Sung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8409884/
https://www.ncbi.nlm.nih.gov/pubmed/33522718
http://dx.doi.org/10.1111/jdi.13516
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author Kim, Hyunah
Lee, Seung‐Hwan
Lee, Hyunyong
Yim, Hyeon Woo
Cho, Jae‐Hyoung
Yoon, Kun‐Ho
Kim, Hun‐Sung
author_facet Kim, Hyunah
Lee, Seung‐Hwan
Lee, Hyunyong
Yim, Hyeon Woo
Cho, Jae‐Hyoung
Yoon, Kun‐Ho
Kim, Hun‐Sung
author_sort Kim, Hyunah
collection PubMed
description AIMS/INTRODUCTION: Increased blood glucose or increased weight is often observed in patients who are prescribed sodium–glucose cotransporter 2 inhibitors (SGLT2i). The aim of this study was to determine in advance which patients, among those prescribed a SGLT2i, would be likely to have improved or worsened blood glucose levels and gain or loss of weight through the use of real‐world data‐based prescriptions. MATERIALS AND METHODS: After 3 months of dapagliflozin prescription, patients were divided into four groups: H(+)W(+) for improved glucose and weight loss; H(+)W(−) for improved blood glucose and weight gain; H(−)W(+) for worsened glucose and weight loss; and H(−)W(−) for worsened glucose and weight gain. RESULTS: The proportion of patients in the H(+)W(+) group was 53.5% (325/608 patients), H(+)W(−) was 19.7% (120/608), H(−)W(+) was 26.8% (114/608) and H(−)W(−) was 8.1% (49/608). The odds of proceeding to H(+)W(−) compared with H(+)W(+), which served as the reference, were 144% in baseline hemoglobin A1c (HbA1c) 7.0–8.0%, 233% in baseline HbA1c 8.0–9.0% and 359% in baseline HbA1c ≥ 9.0% (odds ratio 3.59, P < 0.05) compared with the reference. The odds of proceeding to H(−)W(+) were 29, 13 and 8%, respectively (all P < 0.05), and to H(−)W(−) were 17, 15 and 8%, respectively (all P < 0.05), compared with the reference. The results were expected to vary individually, because changes in blood glucose and bodyweight are more affected by diet and exercise than by drugs. CONCLUSIONS: When first prescribing dapagliflozin, a physician should be aware of the weight gain rather than glucose change if the baseline HbA1c is high, and might concentrate on weight‐related lifestyle training, such as diet and exercise.
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spelling pubmed-84098842021-09-03 Blood glucose levels and bodyweight change after dapagliflozin administration Kim, Hyunah Lee, Seung‐Hwan Lee, Hyunyong Yim, Hyeon Woo Cho, Jae‐Hyoung Yoon, Kun‐Ho Kim, Hun‐Sung J Diabetes Investig Articles AIMS/INTRODUCTION: Increased blood glucose or increased weight is often observed in patients who are prescribed sodium–glucose cotransporter 2 inhibitors (SGLT2i). The aim of this study was to determine in advance which patients, among those prescribed a SGLT2i, would be likely to have improved or worsened blood glucose levels and gain or loss of weight through the use of real‐world data‐based prescriptions. MATERIALS AND METHODS: After 3 months of dapagliflozin prescription, patients were divided into four groups: H(+)W(+) for improved glucose and weight loss; H(+)W(−) for improved blood glucose and weight gain; H(−)W(+) for worsened glucose and weight loss; and H(−)W(−) for worsened glucose and weight gain. RESULTS: The proportion of patients in the H(+)W(+) group was 53.5% (325/608 patients), H(+)W(−) was 19.7% (120/608), H(−)W(+) was 26.8% (114/608) and H(−)W(−) was 8.1% (49/608). The odds of proceeding to H(+)W(−) compared with H(+)W(+), which served as the reference, were 144% in baseline hemoglobin A1c (HbA1c) 7.0–8.0%, 233% in baseline HbA1c 8.0–9.0% and 359% in baseline HbA1c ≥ 9.0% (odds ratio 3.59, P < 0.05) compared with the reference. The odds of proceeding to H(−)W(+) were 29, 13 and 8%, respectively (all P < 0.05), and to H(−)W(−) were 17, 15 and 8%, respectively (all P < 0.05), compared with the reference. The results were expected to vary individually, because changes in blood glucose and bodyweight are more affected by diet and exercise than by drugs. CONCLUSIONS: When first prescribing dapagliflozin, a physician should be aware of the weight gain rather than glucose change if the baseline HbA1c is high, and might concentrate on weight‐related lifestyle training, such as diet and exercise. John Wiley and Sons Inc. 2021-02-28 2021-09 /pmc/articles/PMC8409884/ /pubmed/33522718 http://dx.doi.org/10.1111/jdi.13516 Text en © 2021 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Articles
Kim, Hyunah
Lee, Seung‐Hwan
Lee, Hyunyong
Yim, Hyeon Woo
Cho, Jae‐Hyoung
Yoon, Kun‐Ho
Kim, Hun‐Sung
Blood glucose levels and bodyweight change after dapagliflozin administration
title Blood glucose levels and bodyweight change after dapagliflozin administration
title_full Blood glucose levels and bodyweight change after dapagliflozin administration
title_fullStr Blood glucose levels and bodyweight change after dapagliflozin administration
title_full_unstemmed Blood glucose levels and bodyweight change after dapagliflozin administration
title_short Blood glucose levels and bodyweight change after dapagliflozin administration
title_sort blood glucose levels and bodyweight change after dapagliflozin administration
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8409884/
https://www.ncbi.nlm.nih.gov/pubmed/33522718
http://dx.doi.org/10.1111/jdi.13516
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