Evidence map›Paper›PMID 41121174›Full record

ArticleBMC endocrine disorders2025

Association of serum adiponectin level with glycemic control and atherogenic lipid profile in Sudanese patients with type 2 diabetes mellitus.

Halima Babikir Eltahir, Elmahdi Mohamed Ali, Abdelrahim Osman Mohamed

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Article in BMC endocrine disorders, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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3 · Its place in the literature

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2 citing papers in PubMed.

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5 · Who and what money

Authors and funding

3 authors.

Halima Babikir EltahirDepartment of Biochemistry, Faculty of Medicine, University of Khartoum, P O Box 102, Khartoum, Sudan. halimaeltahir@hotmail.com.
Elmahdi Mohamed AliDepartment of Internal Medicine, Faculty of Medicine, University of Khartoum, Khartoum, Sudan.
Abdelrahim Osman MohamedDepartment of Biochemistry, Faculty of Medicine, University of Khartoum, P O Box 102, Khartoum, Sudan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe pathogenesis of type 2 diabetes mellitus (type 2 DM) involves two major abnormalities: insulin resistance(IR) and impaired insulin secretion, both of which contribute to the inability to regulate blood glucose levels. Adiponectin, a hormone secreted by adipose tissue, plays a role in glucose metabolism and possesses insulin-sensitizing properties. Additionally, adiponectin may play a central role in protecting against atherosclerosis by reducing inflammation, lipid accumulation, and oxidative stress. It has also been reported to increase nitric oxide production in endothelial cells through the activation of nitric oxide synthase. The aim of this study was to investigate the association of serum adiponectin level with glycemic control and atherogenic lipid profile in Sudanese patients with type 2 DM.

methodsThis was a case-control study. Patients with type 2 DM (n = 202) and healthy controls (n = 100) were consented and enrolled. Systolic and diastolic blood pressures (mm Hg), weight (kg), and height (m) were measured, and body mass index (kg/m²) was calculated. Blood samples were collected after an overnight fast. Fasting blood glucose (FBG), haemoglobin A1c (HbA1c), and lipid profile were measured using enzymatic methods. Adiponectin levels were determined using a sandwich ELISA. Multiple regression analysis was conducted to assess the correlation of adiponectin levels with HbA1c and lipid profile parameters.

resultsAdiponectin levels were significantly lower in patients with type 2 DM compared to healthy controls (p < 0.001). Adiponectin was inversely correlated with HbA1c (β = −0.200, p = 0.005), total cholesterol (TC) (β = −0.140, p = 0.044), and low- density lipoprotein cholesterol (LDL-C) (β = −0.162, p = 0.022), and positively correlated with high-density lipoprotein cholesterol (HDL-C) (β = 0.160, p = 0.030). No correlation was observed with triglyceride (TG) levels. Patients with type 2 DM also exhibited significantly higher systolic and diastolic blood pressure, body mass index (BMI), fasting blood glucose (FBG), HbA1c, total cholesterol, and LDL-C levels, along with significantly lower HDL-C levels compared to healthy controls (p < 0.05).

conclusionsPatients with type 2 DM had decreased serum adiponectin levels. The present study supports that adiponectin levels are associated with glycemic control and an atherogenic lipid profile. Adiponectin can be considered clinically relevant both as a potential dual biomarker and as a therapeutic target for glycemic control and atherogenic dyslipidemia in patients with type 2 DM.

Indexed as

AdiponectinAtherosclerosisDiabetes Mellitus, Type 2Glycemic ControlLipidsAdultBiomarkersBlood GlucoseCase-Control StudiesFemaleGlycated HemoglobinHumansMaleMiddle AgedPrognosisSudanAdiponectinADIPOQ protein, humanBiomarkersBlood GlucoseGlycated Hemoglobinhemoglobin A1c protein, humanLipidsAdiponectinAtherogenicHaemoglobin A1cSudanType 2 diabetes mellitus

Identifiers

PMID41121174
PMCPMC12542329

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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.