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Intermediate hyperglycaemia and 10-year mortality in resource-constrained settings: the PERU MIGRANT Study

  • ,
  • A. Ruiz-Alejos
    ,
  • J. J. Miranda
    ,
  • R. M. Carrillo-Larco
    ,
  • R. H. Gilman
    ,
  • L. Smeeth
  • Universidad Peruana Cayetano Heredia
    ,
  • University Hospital
    ,
  • Vanderbilt University
    ,
  • Universidad Peruana Cayetano Heredia
    ,
  • Imperial College London
    ,
  • Johns Hopkins University
Research Output:
Contribution to journal
Article
Peer-review

Open access

Publication Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Pages from-to (Number of pages)

Pages 1519-1527 (9 pages)

Journal (Volume, Issue Number)

Diabetic Medicine (Volume 37, Issue 9)

Publication milestones

  • Published - 01/09/2020

Publication status

Published - 01/09/2020

ISSN

0742-3071

Publication IDs

  • Scopus: 85083043131
  • PubMed: 32181918

Abstract

Aim: To determine whether intermediate hyperglycaemia, defined by fasting plasma glucose and HbA1c criteria, is associated with mortality in a 10-year cohort of people in a Latin American country. Methods: Analysis of the PERU MIGRANT Study was conducted in three different population groups (rural, rural-to-urban migrant, and urban). The baseline assessment was conducted in 2007/2008, with follow-up assessment in 2018. The outcome was all-cause mortality, and the exposure was intermediate hyperglycaemia, using three definitions: (1) impaired fasting glucose, defined according to American Diabetes Association criteria [fasting plasma glucose 5.6–6.9 mmol/l (100–125 mg/dl)]; (2) intermediate hyperglycaemia defined according to American Diabetes Association criteria [HbA1c levels 39–46 mmol/mol (5.7–6.4%)]; and (3) intermediate hyperglycaemia defined according to the International Expert Committee criteria [HbA1c levels 42–46 mmol/mol (6.0–6.4%)]. Crude and adjusted hazard ratios and 95% CIs were estimated using Cox proportional hazard models. Results: At baseline, the mean (sd) age of the study population was 47.8 (11.9) years and 52.5% of the cohort were women. The study cohort was divided into population groups as follows: 207 people (20.0%) in the rural population group, 583 (59.7%) in the rural-to-urban migrant group and 198 (20.3%) in the urban population group. The prevalence of intermediate hyperglycaemia was: 6%, 12.9% and 38.5% according to the American Diabetes Association impaired fasting glucose definition, the International Expert Committee HbA1c-based definition and the American Diabetes Association HbA1c-based definition, respectively, and the mortality rate after 10 years was 63/976 (7%). Intermediate hyperglycaemia was associated with all-cause mortality using the HbA1c-based definitions in the crude models [hazard ratios 2.82 (95% CI 1.59–4.99) according to the American Diabetes Association and 2.92 (95% CI 1.62–5.28) according to the International Expert Committee], whereas American Diabetes Association-defined impaired fasting glucose was not [hazard ratio 0.84 (95% CI 0.26–2.68)]. In the adjusted model, however, only the American Diabetes Association HbA1c-based definition was associated with all-cause mortality [hazard ratio 1.91 (95% CI 1.03–3.53)], whereas the International Expert Committee HbA1c-based and American Diabetes Association impaired fasting glucose-based definitions were not [hazard ratios 1.42 (95% CI 0.75–2.68) and 1.09 (95% CI 0.33–3.63), respectively]. Conclusions: Intermediate hyperglycaemia defined using the American Diabetes Association HbA1c criteria was associated with an elevated mortality rate after 10 years in a cohort from Peru. HbA1c appears to be a factor associated with mortality in this Peruvian population.

Funding Details

The study was funded by a Strategic Award from the Wellcome Trust-Imperial College Centre for Global Health Research (100693/Z/12/Z) and the Imperial College London Wellcome Trust Institutional Strategic Support Fund (Global Health Clinical Research Training Fellowship) (294834/Z ISSF ICL). R.M.C.-L. is supported by a Wellcome Trust International Training Fellowship (214185/Z/18/Z). M.L.-P. receives funding from the Swiss Excellence Government Scholarship (2018.0698). A.B.-O. (103994/Z/14/Z) and J.J.M. (074833/Z/04/Z, 205177/Z/16/Z) are supported by the Wellcome Trust. J.J.M. acknowledges receiving additional support from the Alliance for Health Policy and Systems Research (HQHSR1206660), the Fogarty International Centre (R21TW009982, D71TW010877), Grand Challenges Canada (0335-04), the International Development Research Centre Canada (106887, 108167), the Inter-American Institute for Global Change Research (IAI CRN3036), the Medical Research Council (MR/P008984/1, MR/P024408/1, MR/P02386X/1), the National Cancer Institute (1P20CA217231), the National Heart, Lung and Blood Institute (HHSN268200900033C, 5U01HL114180, 1UM1HL134590), the National Institute of Mental Health (1U19MH098780), the Swiss National Science Foundation (40P740-160366), and the World Diabetes Foundation (WDF15-1224). The study was funded by a Strategic Award from the Wellcome Trust‐Imperial College Centre for Global Health Research (100693/Z/12/Z) and the Imperial College London Wellcome Trust Institutional Strategic Support Fund (Global Health Clinical Research Training Fellowship) (294834/Z ISSF ICL). R.M.C.‐L. is supported by a Wellcome Trust International Training Fellowship (214185/Z/18/Z). M.L.‐P. receives funding from the Swiss Excellence Government Scholarship (2018.0698). A.B.‐O. (103994/Z/14/Z) and J.J.M. (074833/Z/04/Z, 205177/Z/16/Z) are supported by the Wellcome Trust. J.J.M. acknowledges receiving additional support from the Alliance for Health Policy and Systems Research (HQHSR1206660), the Fogarty International Centre (R21TW009982, D71TW010877), Grand Challenges Canada (0335‐04), the International Development Research Centre Canada (106887, 108167), the Inter‐American Institute for Global Change Research (IAI CRN3036), the Medical Research Council (MR/P008984/1, MR/P024408/1, MR/P02386X/1), the National Cancer Institute (1P20CA217231), the National Heart, Lung and Blood Institute (HHSN268200900033C, 5U01HL114180, 1UM1HL134590), the National Institute of Mental Health (1U19MH098780), the Swiss National Science Foundation (40P740‐160366), and the World Diabetes Foundation (WDF15‐1224).
FundersFunding numbers
Imperial College London Wellcome Trust
294834/Z ISSF ICL
Swiss Excellence Government Scholarship
205177/Z/16/Z, 2018.0698, 074833/Z/04/Z, 103994/Z/14/Z
Wellcome Trust‐Imperial College Centre for Global Health Research
-
Wellcome Trust‐Imperial College Centre for Global Health Research
100693/Z/12/Z
NIMH
1U19MH098780
NHLBI
5U01HL114180, HHSN268200900033C, 1UM1HL134590
NCI
1P20CA217231
FIC
R21TW009982, D71TW010877
AHPSR
HQHSR1206660
WT
214185/Z/18/Z
IDRC
108167, 106887
MRC
MR/P02386X/1, MR/P008984/1, MR/P024408/1
SNF
40P740‐160366
GCC
0335‐04
IAI
IAI CRN3036
WDF
WDF15‐1224

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