4.6 Article

Changes in C-reactive protein levels before type 2 diabetes and cardiovascular death: the Whitehall II study

Journal

EUROPEAN JOURNAL OF ENDOCRINOLOGY
Volume 163, Issue 1, Pages 89-95

Publisher

BIOSCIENTIFICA LTD
DOI: 10.1530/EJE-10-0277

Keywords

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Funding

  1. Medical Research Council [G0501184]
  2. Medical Research Council, UK
  3. Economic and Social Research Council, UK
  4. British Heart Foundation, UK
  5. Health and Safety Executive, UK
  6. Department of Health, UK, US
  7. National Heart Lung and Blood Institute, NIH, US [HL36310]
  8. National Institute on Aging, NIH, US [AG13196]
  9. Agency for Health Care Policy Research, US [HS06516]
  10. John D and Catherine T MacArthur Foundation, US
  11. Academy of Finland
  12. BUPA Foundation
  13. MRC [G0902037, G0501184] Funding Source: UKRI
  14. British Heart Foundation [RG/07/008/23674] Funding Source: researchfish
  15. Medical Research Council [G8802774, G0501184, G0100222, G19/35, G0902037] Funding Source: researchfish

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Objective: Prospective studies show that high C-reactive protein (CRP) levels predict diabetes and cardiovascular disease (CVD), but changes in this marker preceding disease onset are not well characterized. This study describes CRP trajectories prior to type 2 diabetes onset and fatal CVD. Methods: In a prospective cohort of 7350 British civil servants (70% male, mean age 51 years), 558 incident type 2 diabetes cases (75-g oral glucose tolerance test, doctor's diagnosis, or self-report) and 125 certified fatal cardiovascular events were observed during a median follow-up of >14 years. Trajectories of logarithmically transformed CRP levels prior to incident diabetes or fatal cardiovascular event (cases), or the end of follow-up (controls) were calculated using multilevel modeling. Results: Baseline CRP levels were higher among participants who developed diabetes (median (interquartile range) 1.44 (2.39) vs 0.78 (1.21) mg/l) or fatal CVD (1.49 (2.47) vs 0.84 (1.30) mg/l) compared with controls (both P<0.0001). In models adjusted for age, sex, body mass index, ethnicity, and employment grade, CRP levels increased with time among both incident diabetes cases and controls (P<0.0001), but this increase was less steep for cases group (P<0.05). CRP levels followed increasing linear trajectories in fatal cardiovascular cases and controls (P<0.0001) with no slope difference between the groups. Conclusions: CRP levels were higher among those who subsequently developed diabetes or died from CVD. For type 2 diabetes, age-related increase in CRP levels was less steep in the cases group than in controls, whereas for fatal CVD these trajectories were parallel.

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