Evidence map›Paper›PMID 40634839›Full record

ArticleBMC cardiovascular disorders2025

High-sensitivity c-reactive protein and cardiovascular disease risk assessment in a population of type 2 diabetes mellitus patients.

Bruno Basil, Jamila Aminu Mohammed, Izuchukwu Nnachi Mba, Blessing Kenechi Myke-Mbata, Joseph Chizoba Akujieze

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Article in BMC cardiovascular disorders, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Bruno BasilInternational Institute of Pathology and Forensic Science Research, David Umahi Federal University of Health Sciences, Uburu, Nigeria.
Jamila Aminu MohammedDepartment of Chemical Pathology, Nile University of Nigeria, Abuja, Nigeria.
Izuchukwu Nnachi MbaDepartment of Chemical Pathology, Nile University of Nigeria, Abuja, Nigeria. mbaizuchukwu@gmail.com.
Blessing Kenechi Myke-MbataDepartment of Chemical Pathology, Benue State University, Makurdi, Nigeria.
Joseph Chizoba AkujiezeDepartment of Medical Laboratory Sciences, University of Jos, Jos, Nigeria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCardiovascular disease (CVD) remains the leading cause of mortality in individuals with type 2 diabetes mellitus (T2DM), driven by chronic hyperglycaemia, dyslipidaemia, and systemic inflammation. In Nigeria, genetic predispositions, ethnic and environmental factors may further modulate CVD risk. This study aimed to evaluate the association between high-sensitivity C-reactive protein (hsCRP) and CVD risk in Nigerian T2DM patients receiving standard care.

methodsThis cross-sectional hospital-based study was conducted over 13 months. Data on socio-demographic characteristics, medical history, clinical findings, and laboratory parameters were collected using a structured proforma. Serum hsCRP was measured by homogenous immunoassay, while 10-year CVD risk was estimated with the WHO CVD risk assessment chart validated for Western sub-Saharan Africa. Statistical analyses, including binary logistic regression to assess the association between hsCRP and CVD risk, were conducted using SPSS version 25, with significance set at p < 0.05.

resultsModerate-to-high CVD risk was prevalent in 51.5% of the study population. Longer diabetes duration (AOR = 1.345, 95% CI: 1.222-1.480, p < 0.001), elevated HbA1c (OR = 1.438, 95% CI: 1.061-1.949, p = 0.019), and co-morbid hypertension (OR = 14.498, 95% CI: 2.611-80.515, p = 0.002) were significantly associated with higher CVD risk. Serum hsCRP levels were higher in moderate-to-high-risk individuals (median: 2.42 mg/L, IQR: 2.8; 2.71 mg/L, IQR: 1.8) compared to lower-risk individuals (median: 1.22 mg/L, IQR: 2.5; 1.48 mg/L, IQR: 2.6), p = 0.012. However, it was not an independent predictor of CVD risk after adjusting for confounders (p = 0.369).

conclusionThere is a high burden of increased CVD risk in this population despite ongoing management, with prolonged diabetes duration, poor glycaemic control and co-morbid hypertension as key predictors. Although hsCRP levels were elevated in higher-risk individuals, its clinical utility as an independent predictor of CVD risk may be limited. These findings emphasize the need to strengthen routine CVD risk assessment, prioritize modifiable risk factors, and optimize glycaemic control to reduce CVD burden in Nigerian T2DM patients.

Indexed as

Cardiovascular DiseasesC-Reactive ProteinDiabetes Mellitus, Type 2Inflammation MediatorsAdultAgedBiomarkersCross-Sectional StudiesFemaleHeart Disease Risk FactorsHumansMaleMiddle AgedNigeriaPrevalencePrognosisBiomarkersC-Reactive ProteinInflammation MediatorsCardiovascular diseaseCVD risk assessmentGlycaemic controlHigh-sensitivity C-reactive proteinNigeria.Type 2 diabetes mellitus

Identifiers

PMID40634839
PMCPMC12239306

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.