Weight changes and their predictors amongst 11 140 patients with type 2 diabetes in the ADVANCE trial
Identifieur interne : 005561 ( Main/Exploration ); précédent : 005560; suivant : 005562Weight changes and their predictors amongst 11 140 patients with type 2 diabetes in the ADVANCE trial
Auteurs : S. Van Dieren [Australie, Pays-Bas] ; S. Czernichow [France] ; J. Chalmers [Australie] ; A. P. Kengne [Australie, Pays-Bas, Afrique du Sud] ; B. E. De Galan [Pays-Bas] ; N. Poulter [Royaume-Uni] ; M. Woodward [Australie] ; J. W. J. Beulens [Pays-Bas] ; D. E. Grobbee [Pays-Bas] ; Y. T. Van Der Schouw [Pays-Bas] ; S. Zoungas [Australie]Source :
- Diabetes, Obesity and Metabolism [ 1462-8902 ] ; 2012-05.
Descripteurs français
- Wicri :
- topic : Collecte de données, Diabète, Glucose.
English descriptors
- KwdEn :
- Advance trial, Alpha glucosidase, Baseline, Baseline characteristics, Baseline predictors, Baseline weight, Blood therapy, Body weight, Cape town, Caucasian, Caucasian ethnicity, Data analysis, Data collection, Diabetes, Diabetes care, Diabetes mellitus, Different patterns, Different regimens, Dual therapy, Effect sizes, Ethnicity, Exclusive indicators, Gain weight, George institute, Gliclazide release, Global health, Glucose, Glucose control, Glycaemic control, Glycemic control, Greatest weight gain, Haemoglobin, Hba1c, Hba1c level, Hypoglycaemic events, Insulin, Insulin combinations, Intensive blood glucose control, Intensive treatment, Intensive treatment arms, Less weight gain, Macrovascular, Macrovascular disease, Medical research council, Metabolism table, Metformin, Metformin thiazol, Microvascular disease, Minimal weight gain, More participants, More patients, Multivariable models, National health, Oral agents, Oral medications, Original article, Original article diabetes, Patient characteristics, Potential predictors, Predictor, Randomized treatment, Sensitivity analysis, Several studies, Standard treatment, Substantial weight gain, Sulphonylurea, Sulphonylurea metformin, Sulphonylurea thiazol, Thiazolidinedione, Treatment allocation, Treatment combinations, Vascular disease, Vascular outcomes, Weight change, Weight changes, Weight gain, Weight gain group, Weight loss.
- Teeft :
- Advance trial, Alpha glucosidase, Baseline, Baseline characteristics, Baseline predictors, Baseline weight, Blood therapy, Body weight, Cape town, Caucasian, Caucasian ethnicity, Data analysis, Data collection, Diabetes, Diabetes care, Diabetes mellitus, Different patterns, Different regimens, Dual therapy, Effect sizes, Ethnicity, Exclusive indicators, Gain weight, George institute, Gliclazide release, Global health, Glucose, Glucose control, Glycaemic control, Glycemic control, Greatest weight gain, Haemoglobin, Hba1c, Hba1c level, Hypoglycaemic events, Insulin, Insulin combinations, Intensive blood glucose control, Intensive treatment, Intensive treatment arms, Less weight gain, Macrovascular, Macrovascular disease, Medical research council, Metabolism table, Metformin, Metformin thiazol, Microvascular disease, Minimal weight gain, More participants, More patients, Multivariable models, National health, Oral agents, Oral medications, Original article, Original article diabetes, Patient characteristics, Potential predictors, Predictor, Randomized treatment, Sensitivity analysis, Several studies, Standard treatment, Substantial weight gain, Sulphonylurea, Sulphonylurea metformin, Sulphonylurea thiazol, Thiazolidinedione, Treatment allocation, Treatment combinations, Vascular disease, Vascular outcomes, Weight change, Weight changes, Weight gain, Weight gain group, Weight loss.
Abstract
Aims: To determine the baseline characteristics and glucose‐lowering therapies associated with weight change among patients with type 2 diabetes.
Url:
DOI: 10.1111/j.1463-1326.2012.01556.x
Affiliations:
- Afrique du Sud, Australie, France, Pays-Bas, Royaume-Uni
- Angleterre, Grand Londres, Gueldre, Nouvelle-Galles du Sud, Utrecht (province), Victoria (État)
- Londres, Melbourne, Nimègue, Sydney, Utrecht
- Université de Sydney
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Le document en format XML
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type="ISSN">1462-8902</idno><idno type="eISSN">1463-1326</idno><imprint><biblScope unit="vol">14</biblScope><biblScope unit="issue">5</biblScope><biblScope unit="page" from="464">464</biblScope><biblScope unit="page" to="469">469</biblScope><biblScope unit="page-count">6</biblScope><publisher>Blackwell Publishing Ltd</publisher><pubPlace>Oxford, UK</pubPlace><date type="published" when="2012-05">2012-05</date></imprint><idno type="ISSN">1462-8902</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">1462-8902</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Advance trial</term><term>Alpha glucosidase</term><term>Baseline</term><term>Baseline characteristics</term><term>Baseline predictors</term><term>Baseline weight</term><term>Blood therapy</term><term>Body weight</term><term>Cape town</term><term>Caucasian</term><term>Caucasian ethnicity</term><term>Data analysis</term><term>Data collection</term><term>Diabetes</term><term>Diabetes care</term><term>Diabetes mellitus</term><term>Different patterns</term><term>Different regimens</term><term>Dual therapy</term><term>Effect sizes</term><term>Ethnicity</term><term>Exclusive indicators</term><term>Gain weight</term><term>George institute</term><term>Gliclazide release</term><term>Global health</term><term>Glucose</term><term>Glucose control</term><term>Glycaemic control</term><term>Glycemic control</term><term>Greatest weight gain</term><term>Haemoglobin</term><term>Hba1c</term><term>Hba1c level</term><term>Hypoglycaemic events</term><term>Insulin</term><term>Insulin combinations</term><term>Intensive blood glucose control</term><term>Intensive treatment</term><term>Intensive treatment arms</term><term>Less weight gain</term><term>Macrovascular</term><term>Macrovascular disease</term><term>Medical research council</term><term>Metabolism table</term><term>Metformin</term><term>Metformin thiazol</term><term>Microvascular disease</term><term>Minimal weight gain</term><term>More participants</term><term>More patients</term><term>Multivariable models</term><term>National health</term><term>Oral agents</term><term>Oral medications</term><term>Original article</term><term>Original article diabetes</term><term>Patient characteristics</term><term>Potential predictors</term><term>Predictor</term><term>Randomized treatment</term><term>Sensitivity analysis</term><term>Several studies</term><term>Standard treatment</term><term>Substantial weight gain</term><term>Sulphonylurea</term><term>Sulphonylurea metformin</term><term>Sulphonylurea thiazol</term><term>Thiazolidinedione</term><term>Treatment allocation</term><term>Treatment combinations</term><term>Vascular disease</term><term>Vascular outcomes</term><term>Weight change</term><term>Weight changes</term><term>Weight gain</term><term>Weight gain group</term><term>Weight loss</term></keywords><keywords scheme="Teeft" xml:lang="en"><term>Advance trial</term><term>Alpha glucosidase</term><term>Baseline</term><term>Baseline characteristics</term><term>Baseline predictors</term><term>Baseline weight</term><term>Blood therapy</term><term>Body weight</term><term>Cape town</term><term>Caucasian</term><term>Caucasian ethnicity</term><term>Data analysis</term><term>Data collection</term><term>Diabetes</term><term>Diabetes care</term><term>Diabetes mellitus</term><term>Different patterns</term><term>Different regimens</term><term>Dual therapy</term><term>Effect sizes</term><term>Ethnicity</term><term>Exclusive indicators</term><term>Gain weight</term><term>George institute</term><term>Gliclazide release</term><term>Global health</term><term>Glucose</term><term>Glucose control</term><term>Glycaemic control</term><term>Glycemic control</term><term>Greatest weight gain</term><term>Haemoglobin</term><term>Hba1c</term><term>Hba1c level</term><term>Hypoglycaemic events</term><term>Insulin</term><term>Insulin combinations</term><term>Intensive blood glucose control</term><term>Intensive treatment</term><term>Intensive treatment arms</term><term>Less weight gain</term><term>Macrovascular</term><term>Macrovascular disease</term><term>Medical research council</term><term>Metabolism table</term><term>Metformin</term><term>Metformin thiazol</term><term>Microvascular disease</term><term>Minimal weight gain</term><term>More participants</term><term>More patients</term><term>Multivariable models</term><term>National health</term><term>Oral agents</term><term>Oral medications</term><term>Original article</term><term>Original article diabetes</term><term>Patient characteristics</term><term>Potential predictors</term><term>Predictor</term><term>Randomized treatment</term><term>Sensitivity analysis</term><term>Several studies</term><term>Standard treatment</term><term>Substantial weight gain</term><term>Sulphonylurea</term><term>Sulphonylurea metformin</term><term>Sulphonylurea thiazol</term><term>Thiazolidinedione</term><term>Treatment allocation</term><term>Treatment combinations</term><term>Vascular disease</term><term>Vascular outcomes</term><term>Weight change</term><term>Weight changes</term><term>Weight gain</term><term>Weight gain group</term><term>Weight loss</term></keywords><keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Collecte de données</term><term>Diabète</term><term>Glucose</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract">Aims: To determine the baseline characteristics and glucose‐lowering therapies associated with weight change among patients with type 2 diabetes.</div></front></TEI><affiliations><list><country><li>Afrique du Sud</li><li>Australie</li><li>France</li><li>Pays-Bas</li><li>Royaume-Uni</li></country><region><li>Angleterre</li><li>Grand Londres</li><li>Gueldre</li><li>Nouvelle-Galles du Sud</li><li>Utrecht (province)</li><li>Victoria 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Van Dieren</name></region><name sortKey="Chalmers, J" sort="Chalmers, J" uniqKey="Chalmers J" first="J." last="Chalmers">J. Chalmers</name><name sortKey="Kengne, A P" sort="Kengne, A P" uniqKey="Kengne A" first="A. P." last="Kengne">A. P. Kengne</name><name sortKey="Woodward, M" sort="Woodward, M" uniqKey="Woodward M" first="M." last="Woodward">M. Woodward</name><name sortKey="Zoungas, S" sort="Zoungas, S" uniqKey="Zoungas S" first="S." last="Zoungas">S. Zoungas</name><name sortKey="Zoungas, S" sort="Zoungas, S" uniqKey="Zoungas S" first="S." last="Zoungas">S. Zoungas</name><name sortKey="Zoungas, S" sort="Zoungas, S" uniqKey="Zoungas S" first="S." last="Zoungas">S. Zoungas</name></country><country name="Pays-Bas"><region name="Utrecht (province)"><name sortKey="Van Dieren, S" sort="Van Dieren, S" uniqKey="Van Dieren S" first="S." last="Van Dieren">S. Van Dieren</name></region><name sortKey="Beulens, J W J" sort="Beulens, J W J" uniqKey="Beulens J" first="J. W. J." last="Beulens">J. W. J. Beulens</name><name sortKey="De Galan, B E" sort="De Galan, B E" uniqKey="De Galan B" first="B. E." last="De Galan">B. E. De Galan</name><name sortKey="Grobbee, D E" sort="Grobbee, D E" uniqKey="Grobbee D" first="D. E." last="Grobbee">D. E. Grobbee</name><name sortKey="Kengne, A P" sort="Kengne, A P" uniqKey="Kengne A" first="A. P." last="Kengne">A. P. Kengne</name><name sortKey="Van Der Schouw, Y T" sort="Van Der Schouw, Y T" uniqKey="Van Der Schouw Y" first="Y. T." last="Van Der Schouw">Y. T. Van Der Schouw</name></country><country name="France"><noRegion><name sortKey="Czernichow, S" sort="Czernichow, S" uniqKey="Czernichow S" first="S." last="Czernichow">S. Czernichow</name></noRegion></country><country name="Afrique du Sud"><noRegion><name sortKey="Kengne, A P" sort="Kengne, A P" uniqKey="Kengne A" first="A. P." last="Kengne">A. P. Kengne</name></noRegion></country><country name="Royaume-Uni"><region name="Angleterre"><name sortKey="Poulter, N" sort="Poulter, N" uniqKey="Poulter N" first="N." last="Poulter">N. Poulter</name></region></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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