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Glycosylated hemoglobin as a screening test for hyperglycemia in antipsychotic-treated patients: a follow-up study

PURPOSE: To assess the point prevalence of undetected prediabetes (preDM) and diabetes mellitus (DM) in patients treated with antipsychotics and to compare metabolic parameters between patients with normoglycemia (NG), preDM, and DM. Furthermore, conversion rates for preDM and DM were determined in...

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Autores principales: Steylen, Pauline MJ, van der Heijden, Frank MMA, Hoogendijk, Witte JG, Verhoeven, Willem MA
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4311678/
https://www.ncbi.nlm.nih.gov/pubmed/25653547
http://dx.doi.org/10.2147/DMSO.S70029
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author Steylen, Pauline MJ
van der Heijden, Frank MMA
Hoogendijk, Witte JG
Verhoeven, Willem MA
author_facet Steylen, Pauline MJ
van der Heijden, Frank MMA
Hoogendijk, Witte JG
Verhoeven, Willem MA
author_sort Steylen, Pauline MJ
collection PubMed
description PURPOSE: To assess the point prevalence of undetected prediabetes (preDM) and diabetes mellitus (DM) in patients treated with antipsychotics and to compare metabolic parameters between patients with normoglycemia (NG), preDM, and DM. Furthermore, conversion rates for preDM and DM were determined in a 1-year follow-up. PATIENTS AND METHODS: In a naturalistic cohort of 169 patients, fasting glucose (FG) and hemoglobin A(1c) (HbA(1c)) criteria were applied at baseline and at follow-up after 1 year. A distinction was made between baseline patients diagnosed according to FG (B-FG) and those diagnosed according to HbA(1c) (B-HbA(1c)). Conversion rates in the 1-year follow-up were compared between B-FG and B-HbA(1c). RESULTS: At baseline, preDM and DM were present in 39% and 8%, respectively. As compared to patients with NG, metabolic syndrome was significantly more prevalent in patients with preDM (62% vs 31%). Although the majority of patients were identified by the FG criterion, HbA(1c) contributed significantly, especially to the number of patients diagnosed with preDM (32%). Regarding the patients with preDM, conversion rates to NG were much higher in the B-FG group than in the B-HbA(1c) group (72% vs 18%). In patients diagnosed with DM, conversion rates were found for B-FG only. CONCLUSION: PreDM and DM are highly prevalent in psychiatric patients treated with antipsychotic drugs. HbA(1c) was shown to be a more stable parameter in identifying psychiatric patients with (an increased risk for) DM, and it should therefore be included in future screening instruments.
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spelling pubmed-43116782015-02-04 Glycosylated hemoglobin as a screening test for hyperglycemia in antipsychotic-treated patients: a follow-up study Steylen, Pauline MJ van der Heijden, Frank MMA Hoogendijk, Witte JG Verhoeven, Willem MA Diabetes Metab Syndr Obes Original Research PURPOSE: To assess the point prevalence of undetected prediabetes (preDM) and diabetes mellitus (DM) in patients treated with antipsychotics and to compare metabolic parameters between patients with normoglycemia (NG), preDM, and DM. Furthermore, conversion rates for preDM and DM were determined in a 1-year follow-up. PATIENTS AND METHODS: In a naturalistic cohort of 169 patients, fasting glucose (FG) and hemoglobin A(1c) (HbA(1c)) criteria were applied at baseline and at follow-up after 1 year. A distinction was made between baseline patients diagnosed according to FG (B-FG) and those diagnosed according to HbA(1c) (B-HbA(1c)). Conversion rates in the 1-year follow-up were compared between B-FG and B-HbA(1c). RESULTS: At baseline, preDM and DM were present in 39% and 8%, respectively. As compared to patients with NG, metabolic syndrome was significantly more prevalent in patients with preDM (62% vs 31%). Although the majority of patients were identified by the FG criterion, HbA(1c) contributed significantly, especially to the number of patients diagnosed with preDM (32%). Regarding the patients with preDM, conversion rates to NG were much higher in the B-FG group than in the B-HbA(1c) group (72% vs 18%). In patients diagnosed with DM, conversion rates were found for B-FG only. CONCLUSION: PreDM and DM are highly prevalent in psychiatric patients treated with antipsychotic drugs. HbA(1c) was shown to be a more stable parameter in identifying psychiatric patients with (an increased risk for) DM, and it should therefore be included in future screening instruments. Dove Medical Press 2015-01-23 /pmc/articles/PMC4311678/ /pubmed/25653547 http://dx.doi.org/10.2147/DMSO.S70029 Text en © 2015 Steylen et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Steylen, Pauline MJ
van der Heijden, Frank MMA
Hoogendijk, Witte JG
Verhoeven, Willem MA
Glycosylated hemoglobin as a screening test for hyperglycemia in antipsychotic-treated patients: a follow-up study
title Glycosylated hemoglobin as a screening test for hyperglycemia in antipsychotic-treated patients: a follow-up study
title_full Glycosylated hemoglobin as a screening test for hyperglycemia in antipsychotic-treated patients: a follow-up study
title_fullStr Glycosylated hemoglobin as a screening test for hyperglycemia in antipsychotic-treated patients: a follow-up study
title_full_unstemmed Glycosylated hemoglobin as a screening test for hyperglycemia in antipsychotic-treated patients: a follow-up study
title_short Glycosylated hemoglobin as a screening test for hyperglycemia in antipsychotic-treated patients: a follow-up study
title_sort glycosylated hemoglobin as a screening test for hyperglycemia in antipsychotic-treated patients: a follow-up study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4311678/
https://www.ncbi.nlm.nih.gov/pubmed/25653547
http://dx.doi.org/10.2147/DMSO.S70029
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