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Design of and rationale for the Japan Diabetes Optimal Integrated Treatment study for 3 major risk factors of cardiovascular diseases (J-DOIT3): a multicenter, open-label, randomized, parallel-group trial

OBJECTIVE: Multifactorial intervention including the management of levels of blood glucose (BG), blood pressure (BP), and lipids has been suggested to decrease cardiovascular disease (CVD) risk. However, the target ideal and feasible levels for these individual parameters have not been fully evaluat...

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Autores principales: Ueki, Kohjiro, Sasako, Takayoshi, Kato, Masayuki, Okazaki, Yukiko, Okahata, Sumie, Katsuyama, Hisayuki, Haraguchi, Mikiko, Morita, Ai, Ohashi, Ken, Hara, Kazuo, Morise, Atsushi, Izumi, Kazuo, Ohashi, Yasuo, Noda, Mitsuhiko, Kadowaki, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4731753/
https://www.ncbi.nlm.nih.gov/pubmed/26843962
http://dx.doi.org/10.1136/bmjdrc-2015-000123
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author Ueki, Kohjiro
Sasako, Takayoshi
Kato, Masayuki
Okazaki, Yukiko
Okahata, Sumie
Katsuyama, Hisayuki
Haraguchi, Mikiko
Morita, Ai
Ohashi, Ken
Hara, Kazuo
Morise, Atsushi
Izumi, Kazuo
Ohashi, Yasuo
Noda, Mitsuhiko
Kadowaki, Takashi
author_facet Ueki, Kohjiro
Sasako, Takayoshi
Kato, Masayuki
Okazaki, Yukiko
Okahata, Sumie
Katsuyama, Hisayuki
Haraguchi, Mikiko
Morita, Ai
Ohashi, Ken
Hara, Kazuo
Morise, Atsushi
Izumi, Kazuo
Ohashi, Yasuo
Noda, Mitsuhiko
Kadowaki, Takashi
author_sort Ueki, Kohjiro
collection PubMed
description OBJECTIVE: Multifactorial intervention including the management of levels of blood glucose (BG), blood pressure (BP), and lipids has been suggested to decrease cardiovascular disease (CVD) risk. However, the target ideal and feasible levels for these individual parameters have not been fully evaluated. In this study, we examine the hypothesis that stricter control compared with the current targets in the Japanese guideline for BG, BP, and lipids could efficiently and safely reduce CVD risk. RESEARCH DESIGN AND METHODS: We screened patients with type 2 diabetes and hypertension and/or dyslipidemia among 81 hospitals in Japan and allocated them into 2 groups: the intensive therapy group (ITG) and the conventional therapy group (CTG). For the 2 respective groups, the target for glycated hemoglobin (HbA1c) is <6.2% (44 mmol/mol) and <6.9% (52 mmol/mol), for BP it is <120/75 mm Hg and <130/80 mm Hg, and for low-density lipoprotein cholesterol it is <80 mg/dL (<70 mg/dL in the presence of CVD history) and <120 mg/dL (<100 mg/dL in the presence of CVD history). The primary end point is the occurrence of CVD events or death by any cause. These patients are scheduled for stepwise intensifications of medication for BG, BP, and lipid control in the ITG, until the number of primary end point events reaches 250. RESULTS: We recruited 2542 patients and randomly allocated 1271 into the ITG and 1271 into the CTG between June 2006 and March 2009. The mean HbA1c was 8.0% (64 mmol/mol) and the mean duration of diabetes was 8.3 years. CONCLUSIONS: This randomized controlled study will test the hypothesis that strict multifactorial intervention therapy is effective for the prevention of CVDs in patients with type 2 diabetes who are at high CVD risk. TRIAL REGISTRATION NUMBER: NCT00300976.
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spelling pubmed-47317532016-02-03 Design of and rationale for the Japan Diabetes Optimal Integrated Treatment study for 3 major risk factors of cardiovascular diseases (J-DOIT3): a multicenter, open-label, randomized, parallel-group trial Ueki, Kohjiro Sasako, Takayoshi Kato, Masayuki Okazaki, Yukiko Okahata, Sumie Katsuyama, Hisayuki Haraguchi, Mikiko Morita, Ai Ohashi, Ken Hara, Kazuo Morise, Atsushi Izumi, Kazuo Ohashi, Yasuo Noda, Mitsuhiko Kadowaki, Takashi BMJ Open Diabetes Res Care Cardiovascular and Metabolic Risk OBJECTIVE: Multifactorial intervention including the management of levels of blood glucose (BG), blood pressure (BP), and lipids has been suggested to decrease cardiovascular disease (CVD) risk. However, the target ideal and feasible levels for these individual parameters have not been fully evaluated. In this study, we examine the hypothesis that stricter control compared with the current targets in the Japanese guideline for BG, BP, and lipids could efficiently and safely reduce CVD risk. RESEARCH DESIGN AND METHODS: We screened patients with type 2 diabetes and hypertension and/or dyslipidemia among 81 hospitals in Japan and allocated them into 2 groups: the intensive therapy group (ITG) and the conventional therapy group (CTG). For the 2 respective groups, the target for glycated hemoglobin (HbA1c) is <6.2% (44 mmol/mol) and <6.9% (52 mmol/mol), for BP it is <120/75 mm Hg and <130/80 mm Hg, and for low-density lipoprotein cholesterol it is <80 mg/dL (<70 mg/dL in the presence of CVD history) and <120 mg/dL (<100 mg/dL in the presence of CVD history). The primary end point is the occurrence of CVD events or death by any cause. These patients are scheduled for stepwise intensifications of medication for BG, BP, and lipid control in the ITG, until the number of primary end point events reaches 250. RESULTS: We recruited 2542 patients and randomly allocated 1271 into the ITG and 1271 into the CTG between June 2006 and March 2009. The mean HbA1c was 8.0% (64 mmol/mol) and the mean duration of diabetes was 8.3 years. CONCLUSIONS: This randomized controlled study will test the hypothesis that strict multifactorial intervention therapy is effective for the prevention of CVDs in patients with type 2 diabetes who are at high CVD risk. TRIAL REGISTRATION NUMBER: NCT00300976. BMJ Publishing Group 2016-01-25 /pmc/articles/PMC4731753/ /pubmed/26843962 http://dx.doi.org/10.1136/bmjdrc-2015-000123 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Cardiovascular and Metabolic Risk
Ueki, Kohjiro
Sasako, Takayoshi
Kato, Masayuki
Okazaki, Yukiko
Okahata, Sumie
Katsuyama, Hisayuki
Haraguchi, Mikiko
Morita, Ai
Ohashi, Ken
Hara, Kazuo
Morise, Atsushi
Izumi, Kazuo
Ohashi, Yasuo
Noda, Mitsuhiko
Kadowaki, Takashi
Design of and rationale for the Japan Diabetes Optimal Integrated Treatment study for 3 major risk factors of cardiovascular diseases (J-DOIT3): a multicenter, open-label, randomized, parallel-group trial
title Design of and rationale for the Japan Diabetes Optimal Integrated Treatment study for 3 major risk factors of cardiovascular diseases (J-DOIT3): a multicenter, open-label, randomized, parallel-group trial
title_full Design of and rationale for the Japan Diabetes Optimal Integrated Treatment study for 3 major risk factors of cardiovascular diseases (J-DOIT3): a multicenter, open-label, randomized, parallel-group trial
title_fullStr Design of and rationale for the Japan Diabetes Optimal Integrated Treatment study for 3 major risk factors of cardiovascular diseases (J-DOIT3): a multicenter, open-label, randomized, parallel-group trial
title_full_unstemmed Design of and rationale for the Japan Diabetes Optimal Integrated Treatment study for 3 major risk factors of cardiovascular diseases (J-DOIT3): a multicenter, open-label, randomized, parallel-group trial
title_short Design of and rationale for the Japan Diabetes Optimal Integrated Treatment study for 3 major risk factors of cardiovascular diseases (J-DOIT3): a multicenter, open-label, randomized, parallel-group trial
title_sort design of and rationale for the japan diabetes optimal integrated treatment study for 3 major risk factors of cardiovascular diseases (j-doit3): a multicenter, open-label, randomized, parallel-group trial
topic Cardiovascular and Metabolic Risk
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4731753/
https://www.ncbi.nlm.nih.gov/pubmed/26843962
http://dx.doi.org/10.1136/bmjdrc-2015-000123
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