A Randomized Controlled Trial of R-Form Verapamil Added to Ongoing Metformin Therapy in Patients with Type 2 Diabetes
Context: There is a medical need for effective insulin-independent antidiabetic drugs that can promote pancreatic [beta]-cell function and have a low risk of hypoglycemia in type 2 diabetes mellitus (T2DM) patients. R-form verapamil (R-Vera), which is able to enhance the survival of [beta]-cells and...
Gespeichert in:
Veröffentlicht in: | The journal of clinical endocrinology and metabolism 2022-10, Vol.107 (10), p.e4063-e4071 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | e4071 |
---|---|
container_issue | 10 |
container_start_page | e4063 |
container_title | The journal of clinical endocrinology and metabolism |
container_volume | 107 |
creator | Wang, Chih-Yuan Huang, Kuo-Chin Lu, Chia-Wen Chu, Chih-Hsun Huang, Chien-Ning Chen, Harn-Shen Lee, I-Te Chen, Jung-Fu Chen, Ching-Chu Chen, Chung-Sen Hsieh, Chang-Hsun Tien, Kai-Jen Chien, Hung-Yu Huang, Yu-Yao Hsu, Jui-Pao Shane, Guang-Tzuu Chang, Ai-Ching Wu, Yen-Chieh Sheu, Wayne Huey-Herng |
description | Context: There is a medical need for effective insulin-independent antidiabetic drugs that can promote pancreatic [beta]-cell function and have a low risk of hypoglycemia in type 2 diabetes mellitus (T2DM) patients. R-form verapamil (R-Vera), which is able to enhance the survival of [beta]-cells and has higher cardiovascular safety margin compared with racemic verapamil, was developed as a novel approach for T2DM treatment. Objective: This randomized, double-blind, placebo-controlled clinical trial was designed to evaluate the efficacy and safety of 3 dosages of R-Vera added to ongoing metformin therapy in T2DM patients who had inadequate glycemic control on metformin alone. Methods: Participants were randomly assigned in an equal ratio to receive R-Vera 450, 300, or 150 mg per day, or matching placebo, in combination with metformin. The primary endpoint was change in hemoglobin A1c (HbA1c) after 12 weeks of treatment. Results: A total of 184 eligible participants were randomized to receive either R-Vera or placebo plus metformin. At week 12, significant reductions in HbA1c were observed for R-Vera 300 mg/day (-0.36, P = 0.0373) and 450 mg/day (-0.45, P = 0.0098) compared with placebo. The reduction in HbA1c correlated with decreasing fasting plasma glucose levels and improved HOMA2-[beta] score. Treatment with R-Vera was well tolerated with no hypoglycemic episodes occurring during the trial. Conclusion: Addition of R-Vera twice daily to ongoing metformin therapy significantly improved glycemic control in T2DM patients. The favorable efficacy and safety profile of R-Vera 300 mg/day can be considered as the appropriate dose for clinical practice. Key Words: R-form verapamil, metformin, type 2 diabetes, HbA1c, antidiabetic drug Abbreviations: AE, adverse event; BMI, body mass index; DM, diabetes mellitus; FPG, fasting plasma glucose; HbA1c, glycated hemoglobin A1c; HDL, high-density lipoprotein; HOMA2-[beta], homeostasis model 2 assessment [beta]-cell; HOMA2-IR, homeostasis model 2 assessment of insulin resistance; LDL, low-density lipoprotein; LS, least squares; R-Vera, R-form verapamil; SBP, systolic blood pressure; T1DM, type 1 diabetes mellitus; T2DM, type 2 diabetes mellitus; TEAE, treatment-emergent adverse event; TXNIP, thioredoxin-interacting protein. |
doi_str_mv | 10.1210/clinem/dgac436 |
format | Article |
fullrecord | <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9516171</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A777587716</galeid><sourcerecordid>A777587716</sourcerecordid><originalsourceid>FETCH-LOGICAL-c434t-4076018d75194a54d29541fd63eceaa51332e21780bd07dbb3f5c87d6f7882d83</originalsourceid><addsrcrecordid>eNptkt9rFDEQx4NY7Nn66nPAF1-2zY_NZvdFOK5WhZZKuYpvIbuZ3YtkkzPJKedfb447BKHkYYbMJ9_MDF-E3lJyRRkl14OzHuZrM-mh5s0LtKBdLSpJO_kSLQhhtOok-36OXqf0gxBa14K_QudcdFSKlizQbokftTdhtn_A4FXwOQbnSrqOVjscRvxY3YY4428Q9VbP1uGlMaWeA37wU7B-wveQx4JYj9ebA7XHJf2qswWfE_5t8wav91vADN9Y3UOGdInORu0SvDnFC_R0-3G9-lzdPXz6slreVWWYOlc1kQ2hrZGiTKVFbVgnajqahsMAWgvKOQNGZUt6Q6Tpez6KoZWmGWXbMtPyC_ThqLvd9TOYoTQUtVPbaGcd9ypoq_6veLtRU_ilOkEbKmkReH8SiOHnDlJWs00DOKc9hF1SrOlkI4Wgh7_eHdFJO1DWj6EoDgdcLaUs25aSNoW6eoYqx8Bsh-BhtOX-uQdDDClFGP91T4k6WEAdLaBOFuB_AUAnpNQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2697675518</pqid></control><display><type>article</type><title>A Randomized Controlled Trial of R-Form Verapamil Added to Ongoing Metformin Therapy in Patients with Type 2 Diabetes</title><source>Oxford University Press Journals All Titles (1996-Current)</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Alma/SFX Local Collection</source><creator>Wang, Chih-Yuan ; Huang, Kuo-Chin ; Lu, Chia-Wen ; Chu, Chih-Hsun ; Huang, Chien-Ning ; Chen, Harn-Shen ; Lee, I-Te ; Chen, Jung-Fu ; Chen, Ching-Chu ; Chen, Chung-Sen ; Hsieh, Chang-Hsun ; Tien, Kai-Jen ; Chien, Hung-Yu ; Huang, Yu-Yao ; Hsu, Jui-Pao ; Shane, Guang-Tzuu ; Chang, Ai-Ching ; Wu, Yen-Chieh ; Sheu, Wayne Huey-Herng</creator><creatorcontrib>Wang, Chih-Yuan ; Huang, Kuo-Chin ; Lu, Chia-Wen ; Chu, Chih-Hsun ; Huang, Chien-Ning ; Chen, Harn-Shen ; Lee, I-Te ; Chen, Jung-Fu ; Chen, Ching-Chu ; Chen, Chung-Sen ; Hsieh, Chang-Hsun ; Tien, Kai-Jen ; Chien, Hung-Yu ; Huang, Yu-Yao ; Hsu, Jui-Pao ; Shane, Guang-Tzuu ; Chang, Ai-Ching ; Wu, Yen-Chieh ; Sheu, Wayne Huey-Herng</creatorcontrib><description>Context: There is a medical need for effective insulin-independent antidiabetic drugs that can promote pancreatic [beta]-cell function and have a low risk of hypoglycemia in type 2 diabetes mellitus (T2DM) patients. R-form verapamil (R-Vera), which is able to enhance the survival of [beta]-cells and has higher cardiovascular safety margin compared with racemic verapamil, was developed as a novel approach for T2DM treatment. Objective: This randomized, double-blind, placebo-controlled clinical trial was designed to evaluate the efficacy and safety of 3 dosages of R-Vera added to ongoing metformin therapy in T2DM patients who had inadequate glycemic control on metformin alone. Methods: Participants were randomly assigned in an equal ratio to receive R-Vera 450, 300, or 150 mg per day, or matching placebo, in combination with metformin. The primary endpoint was change in hemoglobin A1c (HbA1c) after 12 weeks of treatment. Results: A total of 184 eligible participants were randomized to receive either R-Vera or placebo plus metformin. At week 12, significant reductions in HbA1c were observed for R-Vera 300 mg/day (-0.36, P = 0.0373) and 450 mg/day (-0.45, P = 0.0098) compared with placebo. The reduction in HbA1c correlated with decreasing fasting plasma glucose levels and improved HOMA2-[beta] score. Treatment with R-Vera was well tolerated with no hypoglycemic episodes occurring during the trial. Conclusion: Addition of R-Vera twice daily to ongoing metformin therapy significantly improved glycemic control in T2DM patients. The favorable efficacy and safety profile of R-Vera 300 mg/day can be considered as the appropriate dose for clinical practice. Key Words: R-form verapamil, metformin, type 2 diabetes, HbA1c, antidiabetic drug Abbreviations: AE, adverse event; BMI, body mass index; DM, diabetes mellitus; FPG, fasting plasma glucose; HbA1c, glycated hemoglobin A1c; HDL, high-density lipoprotein; HOMA2-[beta], homeostasis model 2 assessment [beta]-cell; HOMA2-IR, homeostasis model 2 assessment of insulin resistance; LDL, low-density lipoprotein; LS, least squares; R-Vera, R-form verapamil; SBP, systolic blood pressure; T1DM, type 1 diabetes mellitus; T2DM, type 2 diabetes mellitus; TEAE, treatment-emergent adverse event; TXNIP, thioredoxin-interacting protein.</description><identifier>ISSN: 0021-972X</identifier><identifier>EISSN: 1945-7197</identifier><identifier>DOI: 10.1210/clinem/dgac436</identifier><identifier>PMID: 35917580</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Antihypertensive drugs ; Care and treatment ; Clinical trials ; Comparative analysis ; Dextrose ; Diabetes therapy ; Glucose ; Glycosylated hemoglobin ; Insulin resistance ; Low density lipoproteins ; Metformin ; Online Only ; Product development ; Type 1 diabetes ; Type 2 diabetes ; Verapamil</subject><ispartof>The journal of clinical endocrinology and metabolism, 2022-10, Vol.107 (10), p.e4063-e4071</ispartof><rights>COPYRIGHT 2022 Oxford University Press</rights><rights>The Author(s) 2022. Published by Oxford University Press on behalf of the Endocrine Society. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c434t-4076018d75194a54d29541fd63eceaa51332e21780bd07dbb3f5c87d6f7882d83</citedby><cites>FETCH-LOGICAL-c434t-4076018d75194a54d29541fd63eceaa51332e21780bd07dbb3f5c87d6f7882d83</cites><orcidid>0000-0002-8805-8340 ; 0000-0002-9143-6533</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids></links><search><creatorcontrib>Wang, Chih-Yuan</creatorcontrib><creatorcontrib>Huang, Kuo-Chin</creatorcontrib><creatorcontrib>Lu, Chia-Wen</creatorcontrib><creatorcontrib>Chu, Chih-Hsun</creatorcontrib><creatorcontrib>Huang, Chien-Ning</creatorcontrib><creatorcontrib>Chen, Harn-Shen</creatorcontrib><creatorcontrib>Lee, I-Te</creatorcontrib><creatorcontrib>Chen, Jung-Fu</creatorcontrib><creatorcontrib>Chen, Ching-Chu</creatorcontrib><creatorcontrib>Chen, Chung-Sen</creatorcontrib><creatorcontrib>Hsieh, Chang-Hsun</creatorcontrib><creatorcontrib>Tien, Kai-Jen</creatorcontrib><creatorcontrib>Chien, Hung-Yu</creatorcontrib><creatorcontrib>Huang, Yu-Yao</creatorcontrib><creatorcontrib>Hsu, Jui-Pao</creatorcontrib><creatorcontrib>Shane, Guang-Tzuu</creatorcontrib><creatorcontrib>Chang, Ai-Ching</creatorcontrib><creatorcontrib>Wu, Yen-Chieh</creatorcontrib><creatorcontrib>Sheu, Wayne Huey-Herng</creatorcontrib><title>A Randomized Controlled Trial of R-Form Verapamil Added to Ongoing Metformin Therapy in Patients with Type 2 Diabetes</title><title>The journal of clinical endocrinology and metabolism</title><description>Context: There is a medical need for effective insulin-independent antidiabetic drugs that can promote pancreatic [beta]-cell function and have a low risk of hypoglycemia in type 2 diabetes mellitus (T2DM) patients. R-form verapamil (R-Vera), which is able to enhance the survival of [beta]-cells and has higher cardiovascular safety margin compared with racemic verapamil, was developed as a novel approach for T2DM treatment. Objective: This randomized, double-blind, placebo-controlled clinical trial was designed to evaluate the efficacy and safety of 3 dosages of R-Vera added to ongoing metformin therapy in T2DM patients who had inadequate glycemic control on metformin alone. Methods: Participants were randomly assigned in an equal ratio to receive R-Vera 450, 300, or 150 mg per day, or matching placebo, in combination with metformin. The primary endpoint was change in hemoglobin A1c (HbA1c) after 12 weeks of treatment. Results: A total of 184 eligible participants were randomized to receive either R-Vera or placebo plus metformin. At week 12, significant reductions in HbA1c were observed for R-Vera 300 mg/day (-0.36, P = 0.0373) and 450 mg/day (-0.45, P = 0.0098) compared with placebo. The reduction in HbA1c correlated with decreasing fasting plasma glucose levels and improved HOMA2-[beta] score. Treatment with R-Vera was well tolerated with no hypoglycemic episodes occurring during the trial. Conclusion: Addition of R-Vera twice daily to ongoing metformin therapy significantly improved glycemic control in T2DM patients. The favorable efficacy and safety profile of R-Vera 300 mg/day can be considered as the appropriate dose for clinical practice. Key Words: R-form verapamil, metformin, type 2 diabetes, HbA1c, antidiabetic drug Abbreviations: AE, adverse event; BMI, body mass index; DM, diabetes mellitus; FPG, fasting plasma glucose; HbA1c, glycated hemoglobin A1c; HDL, high-density lipoprotein; HOMA2-[beta], homeostasis model 2 assessment [beta]-cell; HOMA2-IR, homeostasis model 2 assessment of insulin resistance; LDL, low-density lipoprotein; LS, least squares; R-Vera, R-form verapamil; SBP, systolic blood pressure; T1DM, type 1 diabetes mellitus; T2DM, type 2 diabetes mellitus; TEAE, treatment-emergent adverse event; TXNIP, thioredoxin-interacting protein.</description><subject>Antihypertensive drugs</subject><subject>Care and treatment</subject><subject>Clinical trials</subject><subject>Comparative analysis</subject><subject>Dextrose</subject><subject>Diabetes therapy</subject><subject>Glucose</subject><subject>Glycosylated hemoglobin</subject><subject>Insulin resistance</subject><subject>Low density lipoproteins</subject><subject>Metformin</subject><subject>Online Only</subject><subject>Product development</subject><subject>Type 1 diabetes</subject><subject>Type 2 diabetes</subject><subject>Verapamil</subject><issn>0021-972X</issn><issn>1945-7197</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNptkt9rFDEQx4NY7Nn66nPAF1-2zY_NZvdFOK5WhZZKuYpvIbuZ3YtkkzPJKedfb447BKHkYYbMJ9_MDF-E3lJyRRkl14OzHuZrM-mh5s0LtKBdLSpJO_kSLQhhtOok-36OXqf0gxBa14K_QudcdFSKlizQbokftTdhtn_A4FXwOQbnSrqOVjscRvxY3YY4428Q9VbP1uGlMaWeA37wU7B-wveQx4JYj9ebA7XHJf2qswWfE_5t8wav91vADN9Y3UOGdInORu0SvDnFC_R0-3G9-lzdPXz6slreVWWYOlc1kQ2hrZGiTKVFbVgnajqahsMAWgvKOQNGZUt6Q6Tpez6KoZWmGWXbMtPyC_ThqLvd9TOYoTQUtVPbaGcd9ypoq_6veLtRU_ilOkEbKmkReH8SiOHnDlJWs00DOKc9hF1SrOlkI4Wgh7_eHdFJO1DWj6EoDgdcLaUs25aSNoW6eoYqx8Bsh-BhtOX-uQdDDClFGP91T4k6WEAdLaBOFuB_AUAnpNQ</recordid><startdate>20221001</startdate><enddate>20221001</enddate><creator>Wang, Chih-Yuan</creator><creator>Huang, Kuo-Chin</creator><creator>Lu, Chia-Wen</creator><creator>Chu, Chih-Hsun</creator><creator>Huang, Chien-Ning</creator><creator>Chen, Harn-Shen</creator><creator>Lee, I-Te</creator><creator>Chen, Jung-Fu</creator><creator>Chen, Ching-Chu</creator><creator>Chen, Chung-Sen</creator><creator>Hsieh, Chang-Hsun</creator><creator>Tien, Kai-Jen</creator><creator>Chien, Hung-Yu</creator><creator>Huang, Yu-Yao</creator><creator>Hsu, Jui-Pao</creator><creator>Shane, Guang-Tzuu</creator><creator>Chang, Ai-Ching</creator><creator>Wu, Yen-Chieh</creator><creator>Sheu, Wayne Huey-Herng</creator><general>Oxford University Press</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-8805-8340</orcidid><orcidid>https://orcid.org/0000-0002-9143-6533</orcidid></search><sort><creationdate>20221001</creationdate><title>A Randomized Controlled Trial of R-Form Verapamil Added to Ongoing Metformin Therapy in Patients with Type 2 Diabetes</title><author>Wang, Chih-Yuan ; Huang, Kuo-Chin ; Lu, Chia-Wen ; Chu, Chih-Hsun ; Huang, Chien-Ning ; Chen, Harn-Shen ; Lee, I-Te ; Chen, Jung-Fu ; Chen, Ching-Chu ; Chen, Chung-Sen ; Hsieh, Chang-Hsun ; Tien, Kai-Jen ; Chien, Hung-Yu ; Huang, Yu-Yao ; Hsu, Jui-Pao ; Shane, Guang-Tzuu ; Chang, Ai-Ching ; Wu, Yen-Chieh ; Sheu, Wayne Huey-Herng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c434t-4076018d75194a54d29541fd63eceaa51332e21780bd07dbb3f5c87d6f7882d83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Antihypertensive drugs</topic><topic>Care and treatment</topic><topic>Clinical trials</topic><topic>Comparative analysis</topic><topic>Dextrose</topic><topic>Diabetes therapy</topic><topic>Glucose</topic><topic>Glycosylated hemoglobin</topic><topic>Insulin resistance</topic><topic>Low density lipoproteins</topic><topic>Metformin</topic><topic>Online Only</topic><topic>Product development</topic><topic>Type 1 diabetes</topic><topic>Type 2 diabetes</topic><topic>Verapamil</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Chih-Yuan</creatorcontrib><creatorcontrib>Huang, Kuo-Chin</creatorcontrib><creatorcontrib>Lu, Chia-Wen</creatorcontrib><creatorcontrib>Chu, Chih-Hsun</creatorcontrib><creatorcontrib>Huang, Chien-Ning</creatorcontrib><creatorcontrib>Chen, Harn-Shen</creatorcontrib><creatorcontrib>Lee, I-Te</creatorcontrib><creatorcontrib>Chen, Jung-Fu</creatorcontrib><creatorcontrib>Chen, Ching-Chu</creatorcontrib><creatorcontrib>Chen, Chung-Sen</creatorcontrib><creatorcontrib>Hsieh, Chang-Hsun</creatorcontrib><creatorcontrib>Tien, Kai-Jen</creatorcontrib><creatorcontrib>Chien, Hung-Yu</creatorcontrib><creatorcontrib>Huang, Yu-Yao</creatorcontrib><creatorcontrib>Hsu, Jui-Pao</creatorcontrib><creatorcontrib>Shane, Guang-Tzuu</creatorcontrib><creatorcontrib>Chang, Ai-Ching</creatorcontrib><creatorcontrib>Wu, Yen-Chieh</creatorcontrib><creatorcontrib>Sheu, Wayne Huey-Herng</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The journal of clinical endocrinology and metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Chih-Yuan</au><au>Huang, Kuo-Chin</au><au>Lu, Chia-Wen</au><au>Chu, Chih-Hsun</au><au>Huang, Chien-Ning</au><au>Chen, Harn-Shen</au><au>Lee, I-Te</au><au>Chen, Jung-Fu</au><au>Chen, Ching-Chu</au><au>Chen, Chung-Sen</au><au>Hsieh, Chang-Hsun</au><au>Tien, Kai-Jen</au><au>Chien, Hung-Yu</au><au>Huang, Yu-Yao</au><au>Hsu, Jui-Pao</au><au>Shane, Guang-Tzuu</au><au>Chang, Ai-Ching</au><au>Wu, Yen-Chieh</au><au>Sheu, Wayne Huey-Herng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Randomized Controlled Trial of R-Form Verapamil Added to Ongoing Metformin Therapy in Patients with Type 2 Diabetes</atitle><jtitle>The journal of clinical endocrinology and metabolism</jtitle><date>2022-10-01</date><risdate>2022</risdate><volume>107</volume><issue>10</issue><spage>e4063</spage><epage>e4071</epage><pages>e4063-e4071</pages><issn>0021-972X</issn><eissn>1945-7197</eissn><abstract>Context: There is a medical need for effective insulin-independent antidiabetic drugs that can promote pancreatic [beta]-cell function and have a low risk of hypoglycemia in type 2 diabetes mellitus (T2DM) patients. R-form verapamil (R-Vera), which is able to enhance the survival of [beta]-cells and has higher cardiovascular safety margin compared with racemic verapamil, was developed as a novel approach for T2DM treatment. Objective: This randomized, double-blind, placebo-controlled clinical trial was designed to evaluate the efficacy and safety of 3 dosages of R-Vera added to ongoing metformin therapy in T2DM patients who had inadequate glycemic control on metformin alone. Methods: Participants were randomly assigned in an equal ratio to receive R-Vera 450, 300, or 150 mg per day, or matching placebo, in combination with metformin. The primary endpoint was change in hemoglobin A1c (HbA1c) after 12 weeks of treatment. Results: A total of 184 eligible participants were randomized to receive either R-Vera or placebo plus metformin. At week 12, significant reductions in HbA1c were observed for R-Vera 300 mg/day (-0.36, P = 0.0373) and 450 mg/day (-0.45, P = 0.0098) compared with placebo. The reduction in HbA1c correlated with decreasing fasting plasma glucose levels and improved HOMA2-[beta] score. Treatment with R-Vera was well tolerated with no hypoglycemic episodes occurring during the trial. Conclusion: Addition of R-Vera twice daily to ongoing metformin therapy significantly improved glycemic control in T2DM patients. The favorable efficacy and safety profile of R-Vera 300 mg/day can be considered as the appropriate dose for clinical practice. Key Words: R-form verapamil, metformin, type 2 diabetes, HbA1c, antidiabetic drug Abbreviations: AE, adverse event; BMI, body mass index; DM, diabetes mellitus; FPG, fasting plasma glucose; HbA1c, glycated hemoglobin A1c; HDL, high-density lipoprotein; HOMA2-[beta], homeostasis model 2 assessment [beta]-cell; HOMA2-IR, homeostasis model 2 assessment of insulin resistance; LDL, low-density lipoprotein; LS, least squares; R-Vera, R-form verapamil; SBP, systolic blood pressure; T1DM, type 1 diabetes mellitus; T2DM, type 2 diabetes mellitus; TEAE, treatment-emergent adverse event; TXNIP, thioredoxin-interacting protein.</abstract><cop>US</cop><pub>Oxford University Press</pub><pmid>35917580</pmid><doi>10.1210/clinem/dgac436</doi><orcidid>https://orcid.org/0000-0002-8805-8340</orcidid><orcidid>https://orcid.org/0000-0002-9143-6533</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0021-972X |
ispartof | The journal of clinical endocrinology and metabolism, 2022-10, Vol.107 (10), p.e4063-e4071 |
issn | 0021-972X 1945-7197 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9516171 |
source | Oxford University Press Journals All Titles (1996-Current); Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
subjects | Antihypertensive drugs Care and treatment Clinical trials Comparative analysis Dextrose Diabetes therapy Glucose Glycosylated hemoglobin Insulin resistance Low density lipoproteins Metformin Online Only Product development Type 1 diabetes Type 2 diabetes Verapamil |
title | A Randomized Controlled Trial of R-Form Verapamil Added to Ongoing Metformin Therapy in Patients with Type 2 Diabetes |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-30T20%3A32%3A31IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20Randomized%20Controlled%20Trial%20of%20R-Form%20Verapamil%20Added%20to%20Ongoing%20Metformin%20Therapy%20in%20Patients%20with%20Type%202%20Diabetes&rft.jtitle=The%20journal%20of%20clinical%20endocrinology%20and%20metabolism&rft.au=Wang,%20Chih-Yuan&rft.date=2022-10-01&rft.volume=107&rft.issue=10&rft.spage=e4063&rft.epage=e4071&rft.pages=e4063-e4071&rft.issn=0021-972X&rft.eissn=1945-7197&rft_id=info:doi/10.1210/clinem/dgac436&rft_dat=%3Cgale_pubme%3EA777587716%3C/gale_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2697675518&rft_id=info:pmid/35917580&rft_galeid=A777587716&rfr_iscdi=true |