Risk of treatment-emergent diabetes mellitus in patients receiving antipsychotics
Risk of treatment-emergent diabetes mellitus in patients receiving antipsychotics
BACKGROUND: Type 2 diabetes mellitus has been reported during antipsychotic treatment. OBJECTIVE: To quantify the potential risk of treatment-emergent diabetes mellitus among patients receiving antipsychotic medications. METHODS: The MEDLINE and Psychinfo databases were searched using the key words antipsychotic (including individual drug names), diabetes, risk, and incidence for all English-language articles published between 1966 and 2005. Risk calculations were performed using data obtained from pharmacoepidemiologic studies that met the following criteria: (1) cohort design, (2) determination of preexisting diabetes, (3) inclusion of antipsychotic monotherapy as an exposure variable, and (4) comparison with exposure to first-generation antipsychotics. Studies meeting these criteria were used to calculate incidence, attributable risk between agents, and number needed to harm. RESULTS: A total of 25 observational pharmacoepidemiologic studies were found comparing antipsychotics on the outcome of diabetes mellitus. Sufficient information was provided in 15 of the reports to be able to estimate attributable risk. Attributable risk for individual second-generation antipsychotics relative to first-generation antipsychotics ranged from 53 more to 46 fewer new cases of diabetes per 1000 patients. Little observable difference was noted between the individual second-generation antipsychotics versus first-generation antipsychotics on this outcome. However, few of the studies controlled for body weight, race or ethnicity, or the presence of diabetogenic medications. None adjusted for familial history of diabetes, levels of physical activity, or diet, as this information is not usually available in the databases used in pharmacoepidemiologic studies. CONCLUSIONS: Based on the published pharmacoepidemiologic reports reviewed, the avoidance of diabetes as an outcome cannot be predictably achieved with precision by choice of a second-versus a first-generation antipsychotic. Risk management for new-onset diabetes requires the assessment of established risk factors such as family history, advancing age, non-white ethnicity, diet, central obesity, and level of physical activity.
antipsychotic, diabetes, schizophrenia
1593-1603
Citrome, Leslie L.
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Holt, Richard I.G.
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Zachry, Woodie M.
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Clewell, Jerry D.
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Orth, Paul A.
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Karagianis, Jamie L.
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Hoffmann, Vicki Poole
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October 2007
Citrome, Leslie L.
1f0b719b-5436-4646-9034-edcfa91144df
Holt, Richard I.G.
d54202e1-fcf6-4a17-a320-9f32d7024393
Zachry, Woodie M.
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Clewell, Jerry D.
54a9f5bc-458d-42c7-a6aa-0f0f3106bb28
Orth, Paul A.
2a762baf-cd57-482e-8b76-655821c13c6f
Karagianis, Jamie L.
f6424191-a9a3-4c07-97e1-ccb57331f8d3
Hoffmann, Vicki Poole
4a6976c3-d0b1-4f85-844b-ac886fb65846
Citrome, Leslie L., Holt, Richard I.G., Zachry, Woodie M., Clewell, Jerry D., Orth, Paul A., Karagianis, Jamie L. and Hoffmann, Vicki Poole
(2007)
Risk of treatment-emergent diabetes mellitus in patients receiving antipsychotics.
The Annals of Pharmacotherapy, 41 (10), .
(doi:10.1345/aph.1K141).
Abstract
BACKGROUND: Type 2 diabetes mellitus has been reported during antipsychotic treatment. OBJECTIVE: To quantify the potential risk of treatment-emergent diabetes mellitus among patients receiving antipsychotic medications. METHODS: The MEDLINE and Psychinfo databases were searched using the key words antipsychotic (including individual drug names), diabetes, risk, and incidence for all English-language articles published between 1966 and 2005. Risk calculations were performed using data obtained from pharmacoepidemiologic studies that met the following criteria: (1) cohort design, (2) determination of preexisting diabetes, (3) inclusion of antipsychotic monotherapy as an exposure variable, and (4) comparison with exposure to first-generation antipsychotics. Studies meeting these criteria were used to calculate incidence, attributable risk between agents, and number needed to harm. RESULTS: A total of 25 observational pharmacoepidemiologic studies were found comparing antipsychotics on the outcome of diabetes mellitus. Sufficient information was provided in 15 of the reports to be able to estimate attributable risk. Attributable risk for individual second-generation antipsychotics relative to first-generation antipsychotics ranged from 53 more to 46 fewer new cases of diabetes per 1000 patients. Little observable difference was noted between the individual second-generation antipsychotics versus first-generation antipsychotics on this outcome. However, few of the studies controlled for body weight, race or ethnicity, or the presence of diabetogenic medications. None adjusted for familial history of diabetes, levels of physical activity, or diet, as this information is not usually available in the databases used in pharmacoepidemiologic studies. CONCLUSIONS: Based on the published pharmacoepidemiologic reports reviewed, the avoidance of diabetes as an outcome cannot be predictably achieved with precision by choice of a second-versus a first-generation antipsychotic. Risk management for new-onset diabetes requires the assessment of established risk factors such as family history, advancing age, non-white ethnicity, diet, central obesity, and level of physical activity.
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Published date: October 2007
Keywords:
antipsychotic, diabetes, schizophrenia
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Local EPrints ID: 60990
URI: http://eprints.soton.ac.uk/id/eprint/60990
ISSN: 1060-0280
PURE UUID: 0d39e022-9e8c-4a7a-9051-9952f7a58e46
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Date deposited: 24 Sep 2008
Last modified: 16 Mar 2024 03:19
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Contributors
Author:
Leslie L. Citrome
Author:
Woodie M. Zachry
Author:
Jerry D. Clewell
Author:
Paul A. Orth
Author:
Jamie L. Karagianis
Author:
Vicki Poole Hoffmann
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