Article Text

Original research
Trends in known and undiagnosed diabetes, HbA1c levels, cardiometabolic risk factors and diabetes treatment target achievement in repeated cross-sectional surveys: the population-based Tromsø Study 1994–2016
  1. Petja Lyn Langholz1,
  2. Tom Wilsgaard1,
  3. Inger Njølstad1,
  4. Rolf Jorde2,3,
  5. Laila Arnesdatter Hopstock1
  1. 1Department of Community Medicine, UiT The Arctic University of Norway, Tromsø, Norway
  2. 2Department of Clinical Medicine, UiT The Arctic University of Norway, Tromsø, Norway
  3. 3Division of Internal Medicine, University Hospital of North Norway, Tromsø, Norway
  1. Correspondence to Ms Petja Lyn Langholz; petja.langholz{at}uit.no

Abstract

Objectives The aim of this study was to investigate time trends in known and undiagnosed diabetes, glycated haemoglobin (HbA1c) levels and other cardiometabolic risk factors in the general population as well as treatment target achievement among those with diabetes.

Design and setting Repeated cross-sectional surveys in the population-based Tromsø Study.

Methods We used age-adjusted generalised estimating equation models to study trends in self-reported and undiagnosed (HbA1c ≥6.5%) diabetes, cardiometabolic risk factors and the metabolic syndrome in 27 281 women and men aged 40–84 years examined in up to four surveys of the Tromsø Study between 1994 and 2016. Further, we analysed trends in diabetes treatment target achievement.

Results During 1994–2016, diabetes prevalence increased in women (2.3% to 4.6%) and men (2.4% to 5.8%) and in all age groups, while the proportion of undiagnosed diabetes in women (32% to 17%) and men (37% to 24%) decreased. Blood pressure and total cholesterol decreased, while waist circumference increased in participants with and without diabetes, leading to a relatively stable prevalence of the metabolic syndrome throughout the study period. There was a marginal increase in HbA1c levels among participants without diabetes. Only half of those with diabetes achieved the treatment target of HbA1c ≤7.0%.

Conclusion In the last two decades, diabetes prevalence increased, while the proportion of undiagnosed diabetes declined. The prevalence of the metabolic syndrome remained stable throughout, driven by opposing trends with an increase in obesity and a decrease in other cardiometabolic risk factors. HbA1c treatment target achievement did not improve.

  • diabetes & endocrinology
  • general diabetes
  • epidemiology
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Footnotes

  • Contributors LAH and IN designed the study. RJ and IN contributed to data collection. PLL and TW performed the statistical analysis. All authors contributed to the interpretation of the results. PLL and LAH drafted the manuscript. All authors critically revised the manuscript. All authors read and approved the final manuscript.

  • Funding The study was partly funded by a grant from The Norwegian Diabetes Association. The publication charges for this article have been funded by a grant from the publication fund of UiT The Arctic University of Norway.

  • Disclaimer The funder had no involvement in the study design, collection, analysis and interpretation of data, the writing of the manuscript or the decision to submit the manuscript for publication.

  • Competing interests None declared.

  • Patient consent for publication Not required.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Data availability statement Data may be obtained from a third party and are not publicly available. No additional data available.

  • Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.