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Role of diuretics, β blockers, and statins in increasing the risk of diabetes in patients with impaired glucose tolerance: reanalysis of data from the NAVIGATOR study

Identifieur interne : 004893 ( Main/Exploration ); précédent : 004892; suivant : 004894

Role of diuretics, β blockers, and statins in increasing the risk of diabetes in patients with impaired glucose tolerance: reanalysis of data from the NAVIGATOR study

Auteurs : Lan Shen [États-Unis, République populaire de Chine] ; Bimal R. Shah [États-Unis] ; Eric M. Reyes [États-Unis] ; Laine Thomas [États-Unis] ; Daniel Wojdyla [États-Unis] ; Peter Diem [Suisse, États-Unis] ; Lawrence A. Leiter [Canada, États-Unis] ; Bernard Charbonnel [France, États-Unis] ; Viacheslav Mareev [Russie, États-Unis] ; Edward S. Horton [États-Unis] ; Steven M. Haffner [Royaume-Uni, États-Unis] ; Vladimir Soska [République tchèque, États-Unis] ; Rury Holman [Royaume-Uni, États-Unis] ; M Angelyn Bethel [Royaume-Uni, États-Unis] ; Frank Schaper [Allemagne, États-Unis] ; Jie-Lena Sun [États-Unis] ; John Jv Mcmurray [Royaume-Uni, États-Unis] ; Robert M. Califf [États-Unis] ; Henry Krum [Australie, États-Unis]

Source :

RBID : ISTEX:3FBB3288FDB8558B560FAFE3A176244F8342DB67

Descripteurs français

English descriptors

Abstract

Objective To examine the degree to which use of β blockers, statins, and diuretics in patients with impaired glucose tolerance and other cardiovascular risk factors is associated with new onset diabetes. Design Reanalysis of data from the Nateglinide and Valsartan in Impaired Glucose Tolerance Outcomes Research (NAVIGATOR) trial. Setting NAVIGATOR trial. Participants Patients who at baseline (enrolment) were treatment naïve to β blockers (n=5640), diuretics (n=6346), statins (n=6146), and calcium channel blockers (n=6294). Use of calcium channel blocker was used as a metabolically neutral control. Main outcome measures Development of new onset diabetes diagnosed by standard plasma glucose level in all participants and confirmed with glucose tolerance testing within 12 weeks after the increased glucose value was recorded. The relation between each treatment and new onset diabetes was evaluated using marginal structural models for causal inference, to account for time dependent confounding in treatment assignment. Results During the median five years of follow-up, β blockers were started in 915 (16.2%) patients, diuretics in 1316 (20.7%), statins in 1353 (22.0%), and calcium channel blockers in 1171 (18.6%). After adjusting for baseline characteristics and time varying confounders, diuretics and statins were both associated with an increased risk of new onset diabetes (hazard ratio 1.23, 95% confidence interval 1.06 to 1.44, and 1.32, 1.14 to 1.48, respectively), whereas β blockers and calcium channel blockers were not associated with new onset diabetes (1.10, 0.92 to 1.31, and 0.95, 0.79 to 1.13, respectively). Conclusions Among people with impaired glucose tolerance and other cardiovascular risk factors and with serial glucose measurements, diuretics and statins were associated with an increased risk of new onset diabetes, whereas the effect of β blockers was non-significant. Trial registration ClinicalTrials.gov NCT00097786.

Url:
DOI: 10.1136/bmj.f6745


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<term>Calcium channel blockers</term>
<term>Cardiovascular</term>
<term>Cardiovascular events</term>
<term>Cardiovascular morbidity</term>
<term>Cardiovascular outcomes</term>
<term>Confidence interval</term>
<term>Confounders</term>
<term>Covariate</term>
<term>Data analysis</term>
<term>Data collection</term>
<term>Data interpretation</term>
<term>December</term>
<term>Diabetes</term>
<term>Diabetes mellitus</term>
<term>Diuretic</term>
<term>Endpoint</term>
<term>Extreme weights</term>
<term>Fasting</term>
<term>Glucose</term>
<term>Glucose tolerance</term>
<term>Glucose tolerance outcomes research</term>
<term>Hazard ratio</term>
<term>Heart attack trial</term>
<term>High risk</term>
<term>High risk patients</term>
<term>High risk population</term>
<term>Hypertension</term>
<term>Inverse probability</term>
<term>Lancet</term>
<term>Manuscript review</term>
<term>Mellitus</term>
<term>Model hazard ratio</term>
<term>Navigator</term>
<term>Navigator trial</term>
<term>Novartis</term>
<term>Onset diabetes</term>
<term>Oral glucose tolerance test</term>
<term>Other studies</term>
<term>Previous studies</term>
<term>Randomised</term>
<term>Randomised trial</term>
<term>Reprint</term>
<term>Research institute</term>
<term>Research support</term>
<term>Risk factors</term>
<term>Serial glucose measurements</term>
<term>Statin</term>
<term>Statin therapy</term>
<term>Study design</term>
<term>Treatment initiation</term>
<term>Treatment patients</term>
<term>Treatment weighting</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr">
<term>Collecte de données</term>
<term>Diabète</term>
<term>Glucose</term>
</keywords>
</textClass>
<langUsage>
<language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front>
<div type="abstract">Objective To examine the degree to which use of β blockers, statins, and diuretics in patients with impaired glucose tolerance and other cardiovascular risk factors is associated with new onset diabetes. Design Reanalysis of data from the Nateglinide and Valsartan in Impaired Glucose Tolerance Outcomes Research (NAVIGATOR) trial. Setting NAVIGATOR trial. Participants Patients who at baseline (enrolment) were treatment naïve to β blockers (n=5640), diuretics (n=6346), statins (n=6146), and calcium channel blockers (n=6294). Use of calcium channel blocker was used as a metabolically neutral control. Main outcome measures Development of new onset diabetes diagnosed by standard plasma glucose level in all participants and confirmed with glucose tolerance testing within 12 weeks after the increased glucose value was recorded. The relation between each treatment and new onset diabetes was evaluated using marginal structural models for causal inference, to account for time dependent confounding in treatment assignment. Results During the median five years of follow-up, β blockers were started in 915 (16.2%) patients, diuretics in 1316 (20.7%), statins in 1353 (22.0%), and calcium channel blockers in 1171 (18.6%). After adjusting for baseline characteristics and time varying confounders, diuretics and statins were both associated with an increased risk of new onset diabetes (hazard ratio 1.23, 95% confidence interval 1.06 to 1.44, and 1.32, 1.14 to 1.48, respectively), whereas β blockers and calcium channel blockers were not associated with new onset diabetes (1.10, 0.92 to 1.31, and 0.95, 0.79 to 1.13, respectively). Conclusions Among people with impaired glucose tolerance and other cardiovascular risk factors and with serial glucose measurements, diuretics and statins were associated with an increased risk of new onset diabetes, whereas the effect of β blockers was non-significant. Trial registration ClinicalTrials.gov NCT00097786.</div>
</front>
</TEI>
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<li>Allemagne</li>
<li>Australie</li>
<li>Canada</li>
<li>France</li>
<li>Royaume-Uni</li>
<li>Russie</li>
<li>République populaire de Chine</li>
<li>République tchèque</li>
<li>Suisse</li>
<li>États-Unis</li>
</country>
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<li>Angleterre</li>
<li>Canton de Berne</li>
<li>Caroline du Nord</li>
<li>District de Dresde</li>
<li>District fédéral central</li>
<li>Massachusetts</li>
<li>Moravie</li>
<li>Oxfordshire</li>
<li>Pays de la Loire</li>
<li>Saxe (Land)</li>
<li>Écosse</li>
</region>
<settlement>
<li>Berne</li>
<li>Brno</li>
<li>Dresde</li>
<li>Glasgow</li>
<li>Moscou</li>
<li>Nantes</li>
<li>Oxford</li>
</settlement>
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<li>Université d'Oxford</li>
<li>Université de Berne</li>
<li>Université de Glasgow</li>
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<name sortKey="Califf, Robert M" sort="Califf, Robert M" uniqKey="Califf R" first="Robert M" last="Califf">Robert M. Califf</name>
<name sortKey="Charbonnel, Bernard" sort="Charbonnel, Bernard" uniqKey="Charbonnel B" first="Bernard" last="Charbonnel">Bernard Charbonnel</name>
<name sortKey="Diem, Peter" sort="Diem, Peter" uniqKey="Diem P" first="Peter" last="Diem">Peter Diem</name>
<name sortKey="Haffner, Steven M" sort="Haffner, Steven M" uniqKey="Haffner S" first="Steven M" last="Haffner">Steven M. Haffner</name>
<name sortKey="Holman, Rury" sort="Holman, Rury" uniqKey="Holman R" first="Rury" last="Holman">Rury Holman</name>
<name sortKey="Horton, Edward S" sort="Horton, Edward S" uniqKey="Horton E" first="Edward S" last="Horton">Edward S. Horton</name>
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<name sortKey="Krum, Henry" sort="Krum, Henry" uniqKey="Krum H" first="Henry" last="Krum">Henry Krum</name>
<name sortKey="Krum, Henry" sort="Krum, Henry" uniqKey="Krum H" first="Henry" last="Krum">Henry Krum</name>
<name sortKey="Leiter, Lawrence A" sort="Leiter, Lawrence A" uniqKey="Leiter L" first="Lawrence A" last="Leiter">Lawrence A. Leiter</name>
<name sortKey="Mareev, Viacheslav" sort="Mareev, Viacheslav" uniqKey="Mareev V" first="Viacheslav" last="Mareev">Viacheslav Mareev</name>
<name sortKey="Mcmurray, John Jv" sort="Mcmurray, John Jv" uniqKey="Mcmurray J" first="John Jv" last="Mcmurray">John Jv Mcmurray</name>
<name sortKey="Reyes, Eric M" sort="Reyes, Eric M" uniqKey="Reyes E" first="Eric M" last="Reyes">Eric M. Reyes</name>
<name sortKey="Reyes, Eric M" sort="Reyes, Eric M" uniqKey="Reyes E" first="Eric M" last="Reyes">Eric M. Reyes</name>
<name sortKey="Schaper, Frank" sort="Schaper, Frank" uniqKey="Schaper F" first="Frank" last="Schaper">Frank Schaper</name>
<name sortKey="Shah, Bimal R" sort="Shah, Bimal R" uniqKey="Shah B" first="Bimal R" last="Shah">Bimal R. Shah</name>
<name sortKey="Shah, Bimal R" sort="Shah, Bimal R" uniqKey="Shah B" first="Bimal R" last="Shah">Bimal R. Shah</name>
<name sortKey="Shen, Lan" sort="Shen, Lan" uniqKey="Shen L" first="Lan" last="Shen">Lan Shen</name>
<name sortKey="Soska, Vladimir" sort="Soska, Vladimir" uniqKey="Soska V" first="Vladimir" last="Soska">Vladimir Soska</name>
<name sortKey="Sun, Jie Lena" sort="Sun, Jie Lena" uniqKey="Sun J" first="Jie-Lena" last="Sun">Jie-Lena Sun</name>
<name sortKey="Sun, Jie Lena" sort="Sun, Jie Lena" uniqKey="Sun J" first="Jie-Lena" last="Sun">Jie-Lena Sun</name>
<name sortKey="Thomas, Laine" sort="Thomas, Laine" uniqKey="Thomas L" first="Laine" last="Thomas">Laine Thomas</name>
<name sortKey="Thomas, Laine" sort="Thomas, Laine" uniqKey="Thomas L" first="Laine" last="Thomas">Laine Thomas</name>
<name sortKey="Wojdyla, Daniel" sort="Wojdyla, Daniel" uniqKey="Wojdyla D" first="Daniel" last="Wojdyla">Daniel Wojdyla</name>
<name sortKey="Wojdyla, Daniel" sort="Wojdyla, Daniel" uniqKey="Wojdyla D" first="Daniel" last="Wojdyla">Daniel Wojdyla</name>
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<region name="Canton de Berne">
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<name sortKey="Leiter, Lawrence A" sort="Leiter, Lawrence A" uniqKey="Leiter L" first="Lawrence A" last="Leiter">Lawrence A. Leiter</name>
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<country name="France">
<region name="Pays de la Loire">
<name sortKey="Charbonnel, Bernard" sort="Charbonnel, Bernard" uniqKey="Charbonnel B" first="Bernard" last="Charbonnel">Bernard Charbonnel</name>
</region>
</country>
<country name="Russie">
<region name="District fédéral central">
<name sortKey="Mareev, Viacheslav" sort="Mareev, Viacheslav" uniqKey="Mareev V" first="Viacheslav" last="Mareev">Viacheslav Mareev</name>
</region>
</country>
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<region name="Angleterre">
<name sortKey="Haffner, Steven M" sort="Haffner, Steven M" uniqKey="Haffner S" first="Steven M" last="Haffner">Steven M. Haffner</name>
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</record>

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