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      Diagnosing gestational diabetes mellitus: implications of recent changes in diagnostic criteria and role of glycated haemoglobin (HbA1c)

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          ABSTRACT

          Gestational diabetes mellitus (GDM; approximately 5% of pregnancies) represents the most important risk factor for development of later-onset diabetes mellitus. We examined concordance between GDM diagnosis defined using the original 1999 World Health Organization (WHO) criteria and the more recent 2013 WHO criteria and 2015 National Institute for Health and Care Excellence (NICE) criteria. We studied two groups: a case-control group of 257 GDM positive and 266 GDM negative cases, and an incident cohort 699 GDM positive and 6,231 GDM negative cases. In the incident cohort, GDM prevalence was 3.7% (WHO 1999 criteria), 11.4% (NICE 2015 criteria) and 13.7% (WHO 2013 criteria). Our results showed that a significant number of additional cases are detected using the more recent NICE and WHO criteria than the original 1999 WHO criteria, but these additional cases represent an intermediate group with ‘moderate’ dysglycaemia (abnormal blood glucose levels). Our results also show that use of these newer criteria misses a similar group of intermediate cases that were defined as GDM by the 1999 WHO criteria and that glycated haemoglobin in isolation is unlikely to replace the oral glucose tolerance test in GDM diagnosis.

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          Author and article information

          Contributors
          Role: consultant in diabetes and endocrinology
          Role: clinical biochemist
          Role: diabetes clinical nurse specialist
          Role: research nurse
          Role: professor of clinical biochemistry
          Journal
          Clin Med (Lond)
          Clin Med (Lond)
          RCOP
          Clinical Medicine
          Royal College of Physicians
          1470-2118
          1473-4893
          April 2017
          : 17
          : 2
          : 108-113
          Affiliations
          AUniversity Hospital of North Midlands, Stoke-on-Trent and Centre for Health and Development, Staffordshire University, Stoke-on-Trent, UK
          BUniversity Hospital of North Midlands, Stoke-on-Trent and Institute for Applied Clinical Sciences, Keele University, Stoke-on-Trent, UK
          CUniversity Hospital of North Midlands, Stoke-on-Trent, UK
          DUniversity Hospital of North Midlands, Stoke-on-Trent, UK
          EUniversity Hospital of North Midlands, Stoke-on-Trent and Institute for Applied Clinical Sciences, Keele University, Stoke-on-Trent, UK
          Author notes
          Address for correspondence: Professor Tony Fryer, Department of Clinical Biochemistry, University Hospital of North Midlands NHS Trust, Newcastle Road, Stoke-on-Trent ST4 6QG, UK. Email: Anthony.Fryer@ 123456uhns.nhs.uk
          Article
          PMC6297607 PMC6297607 6297607 clinmedicine
          10.7861/clinmedicine.17-2-108
          6297607
          28365618
          aee6b0e3-6ef3-43fd-a122-2ce3d6b5f71a
          © Royal College of Physicians 2017. All rights reserved.
          History
          Categories
          Original Research

          Clinical guidelines,concordance,gestational diabetes mellitus,glycated haemoglobin,HbA1c,NICE,World Health Organization

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