Differential associations between pre-diabetes, diabetes and stroke occurrence among West Africans.


Journal

Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association
ISSN: 1532-8511
Titre abrégé: J Stroke Cerebrovasc Dis
Pays: United States
ID NLM: 9111633

Informations de publication

Date de publication:
Nov 2022
Historique:
received: 07 04 2022
revised: 16 09 2022
accepted: 18 09 2022
pubmed: 5 10 2022
medline: 27 10 2022
entrez: 4 10 2022
Statut: ppublish

Résumé

There are limited data from Africa on the burden and associations between pre-diabetes (pre-DM), diabetes mellitus (DM) and stroke occurrence in a region experiencing a profound rise in stroke burden. To characterize the associations between stroke and dysglycemic status among West Africans. The Stroke Investigative Research and Educational Network (SIREN) is a multicenter, case-control study involving 15 sites in Ghana and Nigeria. Cases include adults aged ≥18 years with clinical and radiological evidence of an acute stroke. Controls were age-and-gender matched stroke-free adults. Detailed evaluations for vascular factors were performed. Pre-diabetes was defined as HBA1c of 5.7%-6.4% or Fasting blood glucose (FBG) 5.6-7.0 mmol/L and DM as HBA1c >6.5% or FBG>7.0 mmol/L. We used conditional logistic regression to estimate adjusted odds ratios (aOR) with 95% Confidence Interval. Among 2,935 stroke cases the mean age was 60.0 ± 14.2 years with 55.2% being males. By glycemic status, 931 (31.7%) were euglycemic, 633 (21.6%) had Pre-diabetes and 1371 (46.7%) had DM. Of the age- and sex-matched stroke-free controls 69.2% were euglycemic, 13.3% had pre-DM and 17.5% had DM. Pre-DM [aOR (95% CI): 3.68(2.61-5.21)] and DM [4.29 (3.19-5.74)] were independently associated with stroke. The aOR of Pre-DM for ischemic stroke 3.06 (2.01-4.64)] was lower than 4.82 (3.37-6.89) for DM. However, the aOR of Pre-DM for hemorrhagic stroke 6.81 (95% CI: 3.29 - 14.08)] was higher than 3.36 (1.94-5.86) for DM. Furthermore, the aOR of pre-DM for ischemic stroke subtypes were 9.64 (1.30-71.57) for cardio-embolic stroke, 3.64 (1.80-7.34) for small-vessel occlusive disease and 4.63 (0.80-26.65) for large-vessel disease. Pre-DM is strongly and independently associated with stroke in Africans. Improving glycemic control through screening, healthy lifestyle and pharmacotherapy at a population level may be strategic in reducing the rising burden of stroke in Africa.

Sections du résumé

BACKGROUND BACKGROUND
There are limited data from Africa on the burden and associations between pre-diabetes (pre-DM), diabetes mellitus (DM) and stroke occurrence in a region experiencing a profound rise in stroke burden.
PURPOSE OBJECTIVE
To characterize the associations between stroke and dysglycemic status among West Africans.
METHODS METHODS
The Stroke Investigative Research and Educational Network (SIREN) is a multicenter, case-control study involving 15 sites in Ghana and Nigeria. Cases include adults aged ≥18 years with clinical and radiological evidence of an acute stroke. Controls were age-and-gender matched stroke-free adults. Detailed evaluations for vascular factors were performed. Pre-diabetes was defined as HBA1c of 5.7%-6.4% or Fasting blood glucose (FBG) 5.6-7.0 mmol/L and DM as HBA1c >6.5% or FBG>7.0 mmol/L. We used conditional logistic regression to estimate adjusted odds ratios (aOR) with 95% Confidence Interval.
RESULTS RESULTS
Among 2,935 stroke cases the mean age was 60.0 ± 14.2 years with 55.2% being males. By glycemic status, 931 (31.7%) were euglycemic, 633 (21.6%) had Pre-diabetes and 1371 (46.7%) had DM. Of the age- and sex-matched stroke-free controls 69.2% were euglycemic, 13.3% had pre-DM and 17.5% had DM. Pre-DM [aOR (95% CI): 3.68(2.61-5.21)] and DM [4.29 (3.19-5.74)] were independently associated with stroke. The aOR of Pre-DM for ischemic stroke 3.06 (2.01-4.64)] was lower than 4.82 (3.37-6.89) for DM. However, the aOR of Pre-DM for hemorrhagic stroke 6.81 (95% CI: 3.29 - 14.08)] was higher than 3.36 (1.94-5.86) for DM. Furthermore, the aOR of pre-DM for ischemic stroke subtypes were 9.64 (1.30-71.57) for cardio-embolic stroke, 3.64 (1.80-7.34) for small-vessel occlusive disease and 4.63 (0.80-26.65) for large-vessel disease.
CONCLUSION CONCLUSIONS
Pre-DM is strongly and independently associated with stroke in Africans. Improving glycemic control through screening, healthy lifestyle and pharmacotherapy at a population level may be strategic in reducing the rising burden of stroke in Africa.

Identifiants

pubmed: 36194925
pii: S1052-3057(22)00499-2
doi: 10.1016/j.jstrokecerebrovasdis.2022.106805
pmc: PMC9840812
mid: NIHMS1844569
pii:
doi:

Substances chimiques

Glycated Hemoglobin A 0
Blood Glucose 0

Types de publication

Multicenter Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

106805

Subventions

Organisme : FIC NIH HHS
ID : D43 TW012030
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS107900
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS115944
Pays : United States
Organisme : NHGRI NIH HHS
ID : U54 HG007479
Pays : United States

Informations de copyright

Copyright © 2022. Published by Elsevier Inc.

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Auteurs

Fred Stephen Sarfo (FS)

Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.

Bruce Ovbiagele (B)

University of California, San Francisco, CA, USA.

Joshua Akinyemi (J)

College of Medicine, University of Ibadan, Ibadan, Nigeria.

Onoja Akpa (O)

College of Medicine, University of Ibadan, Ibadan, Nigeria.

Albert Akpalu (A)

University of Ghana Medical School, Accra, Ghana.

Kolawole Wahab (K)

University of Ilorin Teaching Hospital, Nigeria.

Godwin Ogbole (G)

College of Medicine, University of Ibadan, Ibadan, Nigeria.

Reginald Obiako (R)

Ahmadu Bello University, Zaria, Nigeria.

Morenikeji Komolafe (M)

Obafemi Awolowo University Teaching Hospital, Ile-Ife, Nigeria.

Lukman Owolabi (L)

Aminu Kano Teaching Hospital, Nigeria.

Godwin Osaigbovo (G)

Delta State University Teaching Hospital, Ogara, Nigeria.

Carolyn Jenkins (C)

Medical University of South Carolina, SC, USA.

Adekunle Fakunle (A)

College of Medicine, University of Ibadan, Ibadan, Nigeria.

Abiodun Adeoye (A)

College of Medicine, University of Ibadan, Ibadan, Nigeria.

Dan Lackland (D)

Medical University of South Carolina, SC, USA.

Donna Arnett (D)

University of Kentucky, USA.

Hemant K Tiwari (HK)

University of Alabama at Birmingham, Birmingham, USA.

Taiwo Olunuga (T)

Federal Medical Centre, Abeokuta, Nigeria.

Ezinne Uvere (E)

College of Medicine, University of Ibadan, Ibadan, Nigeria.

Bimbo Fawale (B)

Obafemi Awolowo University Teaching Hospital, Ile-Ife, Nigeria.

Okechukwu Ogah (O)

College of Medicine, University of Ibadan, Ibadan, Nigeria.

Atinuke Agunloye (A)

College of Medicine, University of Ibadan, Ibadan, Nigeria.

Moyinoluwalogo Faniyan (M)

College of Medicine, University of Ibadan, Ibadan, Nigeria.

Samuel Diala (S)

College of Medicine, University of Ibadan, Ibadan, Nigeria.

Oladele Yinka (O)

College of Medicine, University of Ibadan, Ibadan, Nigeria.

Ruth Laryea (R)

University of Ghana Medical School, Accra, Ghana.

Adeleye Osimhiarherhuo (A)

Federal Medical Centre, Abeokuta, Nigeria.

Cynthia Akinsanya (C)

Federal Medical Centre, Abeokuta, Nigeria.

Adeniyi Abdulwasiu (A)

Federal Medical Centre, Abeokuta, Nigeria.

Josephine Akpalu (J)

University of Ghana Medical School, Accra, Ghana.

Oyedunni Arulogun (O)

College of Medicine, University of Ibadan, Ibadan, Nigeria.

Lambert Appiah (L)

Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.

Hamisu Dambatta (H)

Aminu Kano Teaching Hospital, Nigeria.

Balogun Olayemi (B)

Ahmadu Bello University, Zaria, Nigeria.

Akinola Onasanya (A)

Federal Medical Centre, Abeokuta, Nigeria.

Sulaiman Isah (S)

Aminu Kano Teaching Hospital, Nigeria.

Rufus Akinyemi (R)

Federal Medical Centre, Abeokuta, Nigeria.

Mayowa Owolabi (M)

College of Medicine, University of Ibadan, Ibadan, Nigeria. Electronic address: mayowaowolabi@yahoo.com.

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