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Lipidomic risk score independently and cost-effectively predicts risk of future type 2 diabetes: results from diverse cohorts

BACKGROUND: Detection of type 2 diabetes (T2D) is routinely based on the presence of dysglycemia. Although disturbed lipid metabolism is a hallmark of T2D, the potential of plasma lipidomics as a biomarker of future T2D is unknown. Our objective was to develop and validate a plasma lipidomic risk sc...

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Autores principales: Mamtani, Manju, Kulkarni, Hemant, Wong, Gerard, Weir, Jacquelyn M., Barlow, Christopher K., Dyer, Thomas D., Almasy, Laura, Mahaney, Michael C., Comuzzie, Anthony G., Glahn, David C., Magliano, Dianna J., Zimmet, Paul, Shaw, Jonathan, Williams-Blangero, Sarah, Duggirala, Ravindranath, Blangero, John, Meikle, Peter J., Curran, Joanne E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820916/
https://www.ncbi.nlm.nih.gov/pubmed/27044508
http://dx.doi.org/10.1186/s12944-016-0234-3
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author Mamtani, Manju
Kulkarni, Hemant
Wong, Gerard
Weir, Jacquelyn M.
Barlow, Christopher K.
Dyer, Thomas D.
Almasy, Laura
Mahaney, Michael C.
Comuzzie, Anthony G.
Glahn, David C.
Magliano, Dianna J.
Zimmet, Paul
Shaw, Jonathan
Williams-Blangero, Sarah
Duggirala, Ravindranath
Blangero, John
Meikle, Peter J.
Curran, Joanne E.
author_facet Mamtani, Manju
Kulkarni, Hemant
Wong, Gerard
Weir, Jacquelyn M.
Barlow, Christopher K.
Dyer, Thomas D.
Almasy, Laura
Mahaney, Michael C.
Comuzzie, Anthony G.
Glahn, David C.
Magliano, Dianna J.
Zimmet, Paul
Shaw, Jonathan
Williams-Blangero, Sarah
Duggirala, Ravindranath
Blangero, John
Meikle, Peter J.
Curran, Joanne E.
author_sort Mamtani, Manju
collection PubMed
description BACKGROUND: Detection of type 2 diabetes (T2D) is routinely based on the presence of dysglycemia. Although disturbed lipid metabolism is a hallmark of T2D, the potential of plasma lipidomics as a biomarker of future T2D is unknown. Our objective was to develop and validate a plasma lipidomic risk score (LRS) as a biomarker of future type 2 diabetes and to evaluate its cost-effectiveness for T2D screening. METHODS: Plasma LRS, based on significantly associated lipid species from an array of 319 lipid species, was developed in a cohort of initially T2D-free individuals from the San Antonio Family Heart Study (SAFHS). The LRS derived from SAFHS as well as its recalibrated version were validated in an independent cohort from Australia – the AusDiab cohort. The participants were T2D-free at baseline and followed for 9197 person-years in the SAFHS cohort (n = 771) and 5930 person-years in the AusDiab cohort (n = 644). Statistically and clinically improved T2D prediction was evaluated with established statistical parameters in both cohorts. Modeling studies were conducted to determine whether the use of LRS would be cost-effective for T2D screening. The main outcome measures included accuracy and incremental value of the LRS over routinely used clinical predictors of T2D risk; validation of these results in an independent cohort and cost-effectiveness of including LRS in screening/intervention programs for T2D. RESULTS: The LRS was based on plasma concentration of dihydroceramide 18:0, lysoalkylphosphatidylcholine 22:1 and triacyglycerol 16:0/18:0/18:1. The score predicted future T2D independently of prediabetes with an accuracy of 76 %. Even in the subset of initially euglycemic individuals, the LRS improved T2D prediction. In the AusDiab cohort, the LRS continued to predict T2D significantly and independently. When combined with risk-stratification methods currently used in clinical practice, the LRS significantly improved the model fit (p < 0.001), information content (p < 0.001), discrimination (p < 0.001) and reclassification (p < 0.001) in both cohorts. Modeling studies demonstrated that LRS-based risk-stratification combined with metformin supplementation for high-risk individuals was the most cost-effective strategy for T2D prevention. CONCLUSIONS: Considering the novelty, incremental value and cost-effectiveness of LRS it should be used for risk-stratification of future T2D. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12944-016-0234-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-48209162016-04-06 Lipidomic risk score independently and cost-effectively predicts risk of future type 2 diabetes: results from diverse cohorts Mamtani, Manju Kulkarni, Hemant Wong, Gerard Weir, Jacquelyn M. Barlow, Christopher K. Dyer, Thomas D. Almasy, Laura Mahaney, Michael C. Comuzzie, Anthony G. Glahn, David C. Magliano, Dianna J. Zimmet, Paul Shaw, Jonathan Williams-Blangero, Sarah Duggirala, Ravindranath Blangero, John Meikle, Peter J. Curran, Joanne E. Lipids Health Dis Research BACKGROUND: Detection of type 2 diabetes (T2D) is routinely based on the presence of dysglycemia. Although disturbed lipid metabolism is a hallmark of T2D, the potential of plasma lipidomics as a biomarker of future T2D is unknown. Our objective was to develop and validate a plasma lipidomic risk score (LRS) as a biomarker of future type 2 diabetes and to evaluate its cost-effectiveness for T2D screening. METHODS: Plasma LRS, based on significantly associated lipid species from an array of 319 lipid species, was developed in a cohort of initially T2D-free individuals from the San Antonio Family Heart Study (SAFHS). The LRS derived from SAFHS as well as its recalibrated version were validated in an independent cohort from Australia – the AusDiab cohort. The participants were T2D-free at baseline and followed for 9197 person-years in the SAFHS cohort (n = 771) and 5930 person-years in the AusDiab cohort (n = 644). Statistically and clinically improved T2D prediction was evaluated with established statistical parameters in both cohorts. Modeling studies were conducted to determine whether the use of LRS would be cost-effective for T2D screening. The main outcome measures included accuracy and incremental value of the LRS over routinely used clinical predictors of T2D risk; validation of these results in an independent cohort and cost-effectiveness of including LRS in screening/intervention programs for T2D. RESULTS: The LRS was based on plasma concentration of dihydroceramide 18:0, lysoalkylphosphatidylcholine 22:1 and triacyglycerol 16:0/18:0/18:1. The score predicted future T2D independently of prediabetes with an accuracy of 76 %. Even in the subset of initially euglycemic individuals, the LRS improved T2D prediction. In the AusDiab cohort, the LRS continued to predict T2D significantly and independently. When combined with risk-stratification methods currently used in clinical practice, the LRS significantly improved the model fit (p < 0.001), information content (p < 0.001), discrimination (p < 0.001) and reclassification (p < 0.001) in both cohorts. Modeling studies demonstrated that LRS-based risk-stratification combined with metformin supplementation for high-risk individuals was the most cost-effective strategy for T2D prevention. CONCLUSIONS: Considering the novelty, incremental value and cost-effectiveness of LRS it should be used for risk-stratification of future T2D. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12944-016-0234-3) contains supplementary material, which is available to authorized users. BioMed Central 2016-04-04 /pmc/articles/PMC4820916/ /pubmed/27044508 http://dx.doi.org/10.1186/s12944-016-0234-3 Text en © Mamtani et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Mamtani, Manju
Kulkarni, Hemant
Wong, Gerard
Weir, Jacquelyn M.
Barlow, Christopher K.
Dyer, Thomas D.
Almasy, Laura
Mahaney, Michael C.
Comuzzie, Anthony G.
Glahn, David C.
Magliano, Dianna J.
Zimmet, Paul
Shaw, Jonathan
Williams-Blangero, Sarah
Duggirala, Ravindranath
Blangero, John
Meikle, Peter J.
Curran, Joanne E.
Lipidomic risk score independently and cost-effectively predicts risk of future type 2 diabetes: results from diverse cohorts
title Lipidomic risk score independently and cost-effectively predicts risk of future type 2 diabetes: results from diverse cohorts
title_full Lipidomic risk score independently and cost-effectively predicts risk of future type 2 diabetes: results from diverse cohorts
title_fullStr Lipidomic risk score independently and cost-effectively predicts risk of future type 2 diabetes: results from diverse cohorts
title_full_unstemmed Lipidomic risk score independently and cost-effectively predicts risk of future type 2 diabetes: results from diverse cohorts
title_short Lipidomic risk score independently and cost-effectively predicts risk of future type 2 diabetes: results from diverse cohorts
title_sort lipidomic risk score independently and cost-effectively predicts risk of future type 2 diabetes: results from diverse cohorts
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820916/
https://www.ncbi.nlm.nih.gov/pubmed/27044508
http://dx.doi.org/10.1186/s12944-016-0234-3
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