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      Risk scores for type 2 diabetes mellitus in Latin America: a systematic review of population‐based studies

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          Abstract

          Aim

          To summarize the evidence on diabetes risk scores for Latin American populations.

          Methods

          A systematic review was conducted ( CRD42019122306) looking for diagnostic and prognostic models for type 2 diabetes mellitus among randomly selected adults in Latin America. Five databases ( LILACS, Scopus, MEDLINE, Embase and Global Health) were searched. type 2 diabetes mellitus was defined using at least one blood biomarker and the reports needed to include information on the development and/or validation of a multivariable regression model. Risk of bias was assessed using the PROBAST guidelines.

          Results

          Of the 1500 reports identified, 11 were studied in detail and five were included in the qualitative analysis. Two reports were from Mexico, two from Peru and one from Brazil. The number of diabetes cases varied from 48 to 207 in the derivations models, and between 29 and 582 in the validation models. The most common predictors were age, waist circumference and family history of diabetes, and only one study used oral glucose tolerance test as the outcome. The discrimination performance across studies was ~ 70% (range: 66–72%) as per the area under the receiving‐operator curve, the highest metric was always the negative predictive value. Sensitivity was always higher than specificity.

          Conclusion

          There is no evidence to support the use of one risk score throughout Latin America. The development, validation and implementation of risk scores should be a research and public health priority in Latin America to improve type 2 diabetes mellitus screening and prevention.

          What's new?

          • Risk scores are tools that could support screening, diagnosis and prognosis decisions in clinical medicine and public health.

          • Risk scores for undiagnosed diabetes or to predict diabetes are available worldwide with a few in Latin America. However, the characteristics of risk scores available for Latin America, their performance, pitfalls and other attributes have not been summarized or appraised.

          • A lack of synthesized information makes it difficult to understand the strengths and limitations of the available tools, hampering their implementation in clinical and screening guidelines.

          • We conducted a thorough search for risk scores for type 2 diabetes developed in Latin America, providing the clinical and public health communities with evidence to inform their decisions regarding these risk scores.

          • Local and regional health organizations could recommend one risk score or foster the development of a stronger tool to overcome the limitations signalled herein.

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          Most cited references18

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          PROBAST: A Tool to Assess Risk of Bias and Applicability of Prediction Model Studies: Explanation and Elaboration

          Prediction models in health care use predictors to estimate for an individual the probability that a condition or disease is already present (diagnostic model) or will occur in the future (prognostic model). Publications on prediction models have become more common in recent years, and competing prediction models frequently exist for the same outcome or target population. Health care providers, guideline developers, and policymakers are often unsure which model to use or recommend, and in which persons or settings. Hence, systematic reviews of these studies are increasingly demanded, required, and performed. A key part of a systematic review of prediction models is examination of risk of bias and applicability to the intended population and setting. To help reviewers with this process, the authors developed PROBAST (Prediction model Risk Of Bias ASsessment Tool) for studies developing, validating, or updating (for example, extending) prediction models, both diagnostic and prognostic. PROBAST was developed through a consensus process involving a group of experts in the field. It includes 20 signaling questions across 4 domains (participants, predictors, outcome, and analysis). This explanation and elaboration document describes the rationale for including each domain and signaling question and guides researchers, reviewers, readers, and guideline developers in how to use them to assess risk of bias and applicability concerns. All concepts are illustrated with published examples across different topics. The latest version of the PROBAST checklist, accompanying documents, and filled-in examples can be downloaded from www.probast.org.
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            Risk models and scores for type 2 diabetes: systematic review

            Objective To evaluate current risk models and scores for type 2 diabetes and inform selection and implementation of these in practice. Design Systematic review using standard (quantitative) and realist (mainly qualitative) methodology. Inclusion criteria Papers in any language describing the development or external validation, or both, of models and scores to predict the risk of an adult developing type 2 diabetes. Data sources Medline, PreMedline, Embase, and Cochrane databases were searched. Included studies were citation tracked in Google Scholar to identify follow-on studies of usability or impact. Data extraction Data were extracted on statistical properties of models, details of internal or external validation, and use of risk scores beyond the studies that developed them. Quantitative data were tabulated to compare model components and statistical properties. Qualitative data were analysed thematically to identify mechanisms by which use of the risk model or score might improve patient outcomes. Results 8864 titles were scanned, 115 full text papers considered, and 43 papers included in the final sample. These described the prospective development or validation, or both, of 145 risk prediction models and scores, 94 of which were studied in detail here. They had been tested on 6.88 million participants followed for up to 28 years. Heterogeneity of primary studies precluded meta-analysis. Some but not all risk models or scores had robust statistical properties (for example, good discrimination and calibration) and had been externally validated on a different population. Genetic markers added nothing to models over clinical and sociodemographic factors. Most authors described their score as “simple” or “easily implemented,” although few were specific about the intended users and under what circumstances. Ten mechanisms were identified by which measuring diabetes risk might improve outcomes. Follow-on studies that applied a risk score as part of an intervention aimed at reducing actual risk in people were sparse. Conclusion Much work has been done to develop diabetes risk models and scores, but most are rarely used because they require tests not routinely available or they were developed without a specific user or clear use in mind. Encouragingly, recent research has begun to tackle usability and the impact of diabetes risk scores. Two promising areas for further research are interventions that prompt lay people to check their own diabetes risk and use of risk scores on population datasets to identify high risk “hotspots” for targeted public health interventions.
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              A novel risk score to predict cardiovascular disease risk in national populations (Globorisk): a pooled analysis of prospective cohorts and health examination surveys.

              Treatment of cardiovascular risk factors based on disease risk depends on valid risk prediction equations. We aimed to develop, and apply in example countries, a risk prediction equation for cardiovascular disease (consisting here of coronary heart disease and stroke) that can be recalibrated and updated for application in different countries with routinely available information.
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                Author and article information

                Contributors
                rcarrill@ic.ac.uk
                Journal
                Diabet Med
                Diabet. Med
                10.1111/(ISSN)1464-5491
                DME
                Diabetic Medicine
                John Wiley and Sons Inc. (Hoboken )
                0742-3071
                1464-5491
                06 September 2019
                December 2019
                : 36
                : 12 ( doiID: 10.1111/dme.v36.12 )
                : 1573-1584
                Affiliations
                [ 1 ] Department of Epidemiology and Biostatistics School of Public Health Imperial College London London UK
                [ 2 ] CRONICAS Centre of Excellence in Chronic Diseases Universidad Peruana Cayetano Heredia Lima Perú
                [ 3 ] Universidad Científica del Sur Lima Perú
                [ 4 ] Centro de Estudios de Poblacion Universidad Catolica los Ángeles de Chimbote (ULADECHCatolica) Chimbote Perú
                [ 5 ] Facultad de Medicina Humana Universidad Nacional del Centro del Perú Huancayo Perú
                [ 6 ] Department of Medical and Population Health Sciences Research Herbert Wertheim College of Medicine Florida International University Miami FL USA
                [ 7 ] Department of Public Health Faculty of Medicine University of Helsinki Helsinki Finland
                [ 8 ] Faculty of Medicine Riga Stradins University Riga Latvia
                Author notes
                [*] [* ] Correspondence to: Rodrigo M. Carrillo‐Larco. E‐mail: rcarrill@ 123456ic.ac.uk
                [*]

                These authors contributed equally to this work

                Author information
                https://orcid.org/0000-0002-2090-1856
                https://orcid.org/0000-0002-6834-1376
                Article
                DME14114
                10.1111/dme.14114
                6900051
                31441090
                83b0211a-e0c4-4810-be37-29a59a126d27
                © 2019 The Authors. Diabetic Medicine published by John Wiley & Sons Ltd on behalf of Diabetes UK.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 20 August 2019
                Page count
                Figures: 4, Tables: 2, Pages: 12, Words: 7716
                Funding
                Funded by: Wellcome Trust , open-funder-registry 10.13039/100004440;
                Award ID: 214185/Z/18/Z
                Categories
                Systematic Review or Meta‐analysis
                Systematic Reviews or Meta‐analyses
                Custom metadata
                2.0
                December 2019
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.7.2 mode:remove_FC converted:05.12.2019

                Endocrinology & Diabetes
                Endocrinology & Diabetes

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