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Iran Diabetes Research Roadmap (Idrr) Study; Knowledge Gap in Genetic Research on Diabetes Mellitus in Iran: A Review Article



Bandarian F1 ; Omidvar M2 ; Razi F3 ; Nasliesfahani E4 ; Saeedi S5 ; Larijani B6
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Authors Affiliations
  1. 1. Diabetes Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Toronto Rehabilitation Institute-University Health Network, Brain and Spinal Cord Rehabilitation, Toronto, ON, Canada
  3. 3. Obesity and Eating Habits Research Center, Endocrinology and Metabolism Molecular -Cellular Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Elderly Health Research Center, Endocrinology and Metabolism Population Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran
  5. 5. Metabolic Disorders Research Center, Endocrinology and Metabolism Molecular -Cellular Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran
  6. 6. Endocrinology and Metabolism Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran

Source: Iranian Journal of Public Health Published:2017

Abstract

Background: Diabetes mellitus (DM) is the most common metabolic disorder worldwide. This study aimed to report characteristics of genetic studies in DM in Iran and to identify knowledge gap in genetics of diabetes in Iran. Methods: All publications of Iranian authors in national and international journals up to 2015 were included. Comprehensive search was performed in PubMed, Web of Science, Scopus, SID, IranMedex and Magiran using Di-abetes mellitus and Iran* keywords and their combination. This search obtained 25589 documents. The obtained documents were categorized into eleven groups of complications, comorbidity, management, psychology, nutrition, physical activity, genetics, basic sciences, prevention, education and gestational diabetes mellitus (GDM). Documents were categorized based on publication year, WHO and Australian National Health and Medical Research Council (NHMRC) classification, study design and subject area. Results: After screening, 293 documents remained. The trend of publications was increasing and reached peak in 2013. Case-control was the most common method used in the documents. Most of the studies were association study with case-control design while there was no genome-wide association study (GWAS). Genetic risk factors for DM and its complications were the most common topics in the obtained documents followed by DM management. Conclusion: The most of genetic studies in diabetes in Iran are association studies about genetic risk factors of diabetes while GWAS and pharmacogenetic studies are rare or absent. This may indicate low priority of personalized medicine in the field of diabetes in Iran. © 2017, Iranian Journal of Public Health. All rights reserved.
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