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Effectiveness of long-term treatment with SGLT2 inhibitors: real-world evidence from a specialized diabetes center

BACKGROUND: Diabetes is a progressive disease needing multiple drugs for achieving and maintaining good glycemic control. Sodium-glucose co-transporter 2 inhibitors (SGLT2i) is a novel class of anti-diabetic agent which offers several beneficial effects. However, the long-term effectiveness in clini...

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Autores principales: Thewjitcharoen, Yotsapon, Yenseung, Nalin, Malidaeng, Areeya, Nakasatien, Soontaree, Chotwanvirat, Phawinpon, Krittiyawong, Sirinate, Wanothayaroj, Ekgaluck, Himathongkam, Thep
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5709980/
https://www.ncbi.nlm.nih.gov/pubmed/29213337
http://dx.doi.org/10.1186/s13098-017-0297-y
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author Thewjitcharoen, Yotsapon
Yenseung, Nalin
Malidaeng, Areeya
Nakasatien, Soontaree
Chotwanvirat, Phawinpon
Krittiyawong, Sirinate
Wanothayaroj, Ekgaluck
Himathongkam, Thep
author_facet Thewjitcharoen, Yotsapon
Yenseung, Nalin
Malidaeng, Areeya
Nakasatien, Soontaree
Chotwanvirat, Phawinpon
Krittiyawong, Sirinate
Wanothayaroj, Ekgaluck
Himathongkam, Thep
author_sort Thewjitcharoen, Yotsapon
collection PubMed
description BACKGROUND: Diabetes is a progressive disease needing multiple drugs for achieving and maintaining good glycemic control. Sodium-glucose co-transporter 2 inhibitors (SGLT2i) is a novel class of anti-diabetic agent which offers several beneficial effects. However, the long-term effectiveness in clinical practice and safety data of SGLT2 inhibitors is limited, especially in Asian patients. To better understand the effectiveness of SGLT2i in clinical practice, we conducted a retrospective evaluation of patients with diabetes on SGLT2i. METHODS: This retrospective observational study uses data of patients with diabetes who had been prescribed SGLT2i and continued to use at least 6 months at Theptarin Hospital, Bangkok. The characteristics of patients, changes in glycemic control and body weight at 3, 6, 12, 18, 24 months and the last follow-up were evaluated. RESULTS: A total of 189 patients with diabetes (females 50.3%, mean age 59.9 ± 12.3 years, T2DM 97.3%, duration of diabetes 16.3 ± 9.2 years, baseline BMI 29.9 ± 6.1 kg/m(2), baseline HbA(1c) 8.8 ± 1.6%) were prescribed SGLT2i during the study period. At the time of first SGLT2i prescription, 80.4% used three or more other anti-diabetic agents concomitantly and 34.6% used insulin concomitantly. 151 patients who continue to use at least 6 months were included in analysis. At the last follow-up (median time 16 months), overall median HbA(1c) reduction and weight reduction were 1.0% and 1.5 kg, respectively. While glycemic control could maintain up to 18 months, weight loss gradually rebounded after the first 6 months and then backed to baseline body weight at 18 months (78.2 ± 18.0 kg vs. 78.0 ± 17.8, p value = 0.324). The incidence of adverse drug reactions of special interest (polyuria, volume depletion-related events, urinary tract infection, genital infection, and hypoglycemia) was 2.1, 1.6, 2.1, 2.6, and 7.9%, respectively. DISCUSSION: This real-world study confirmed long-term durability of glycemic control with SGLT2i in not only monotherapy, but also add-on studies with other oral anti-diabetic drugs and/or insulin treatment. However, weight loss became evident early after 6 weeks then reached slightly rebounds after 24 weeks until the end of follow-up. Further studies should be done towards a better understanding of treatment with SGLT2i in routine clinical practice.
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spelling pubmed-57099802017-12-06 Effectiveness of long-term treatment with SGLT2 inhibitors: real-world evidence from a specialized diabetes center Thewjitcharoen, Yotsapon Yenseung, Nalin Malidaeng, Areeya Nakasatien, Soontaree Chotwanvirat, Phawinpon Krittiyawong, Sirinate Wanothayaroj, Ekgaluck Himathongkam, Thep Diabetol Metab Syndr Research BACKGROUND: Diabetes is a progressive disease needing multiple drugs for achieving and maintaining good glycemic control. Sodium-glucose co-transporter 2 inhibitors (SGLT2i) is a novel class of anti-diabetic agent which offers several beneficial effects. However, the long-term effectiveness in clinical practice and safety data of SGLT2 inhibitors is limited, especially in Asian patients. To better understand the effectiveness of SGLT2i in clinical practice, we conducted a retrospective evaluation of patients with diabetes on SGLT2i. METHODS: This retrospective observational study uses data of patients with diabetes who had been prescribed SGLT2i and continued to use at least 6 months at Theptarin Hospital, Bangkok. The characteristics of patients, changes in glycemic control and body weight at 3, 6, 12, 18, 24 months and the last follow-up were evaluated. RESULTS: A total of 189 patients with diabetes (females 50.3%, mean age 59.9 ± 12.3 years, T2DM 97.3%, duration of diabetes 16.3 ± 9.2 years, baseline BMI 29.9 ± 6.1 kg/m(2), baseline HbA(1c) 8.8 ± 1.6%) were prescribed SGLT2i during the study period. At the time of first SGLT2i prescription, 80.4% used three or more other anti-diabetic agents concomitantly and 34.6% used insulin concomitantly. 151 patients who continue to use at least 6 months were included in analysis. At the last follow-up (median time 16 months), overall median HbA(1c) reduction and weight reduction were 1.0% and 1.5 kg, respectively. While glycemic control could maintain up to 18 months, weight loss gradually rebounded after the first 6 months and then backed to baseline body weight at 18 months (78.2 ± 18.0 kg vs. 78.0 ± 17.8, p value = 0.324). The incidence of adverse drug reactions of special interest (polyuria, volume depletion-related events, urinary tract infection, genital infection, and hypoglycemia) was 2.1, 1.6, 2.1, 2.6, and 7.9%, respectively. DISCUSSION: This real-world study confirmed long-term durability of glycemic control with SGLT2i in not only monotherapy, but also add-on studies with other oral anti-diabetic drugs and/or insulin treatment. However, weight loss became evident early after 6 weeks then reached slightly rebounds after 24 weeks until the end of follow-up. Further studies should be done towards a better understanding of treatment with SGLT2i in routine clinical practice. BioMed Central 2017-12-01 /pmc/articles/PMC5709980/ /pubmed/29213337 http://dx.doi.org/10.1186/s13098-017-0297-y Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Thewjitcharoen, Yotsapon
Yenseung, Nalin
Malidaeng, Areeya
Nakasatien, Soontaree
Chotwanvirat, Phawinpon
Krittiyawong, Sirinate
Wanothayaroj, Ekgaluck
Himathongkam, Thep
Effectiveness of long-term treatment with SGLT2 inhibitors: real-world evidence from a specialized diabetes center
title Effectiveness of long-term treatment with SGLT2 inhibitors: real-world evidence from a specialized diabetes center
title_full Effectiveness of long-term treatment with SGLT2 inhibitors: real-world evidence from a specialized diabetes center
title_fullStr Effectiveness of long-term treatment with SGLT2 inhibitors: real-world evidence from a specialized diabetes center
title_full_unstemmed Effectiveness of long-term treatment with SGLT2 inhibitors: real-world evidence from a specialized diabetes center
title_short Effectiveness of long-term treatment with SGLT2 inhibitors: real-world evidence from a specialized diabetes center
title_sort effectiveness of long-term treatment with sglt2 inhibitors: real-world evidence from a specialized diabetes center
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5709980/
https://www.ncbi.nlm.nih.gov/pubmed/29213337
http://dx.doi.org/10.1186/s13098-017-0297-y
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