Key result
Higher atherogenic index of plasma discriminates type 2 diabetes with an AUC of ~0.82.
Why the study?
The atherogenic index of plasma is an inexpensive composite marker of atherogenic lipid risk in patients with type 2 diabetes mellitus, but case-control data quantifying its performance in Sudanese adults with T2DM were lacking.
Does the Atherogenic Index of Plasma (AIP) accurately discriminate Type 2 Diabetes Mellitus status and independently reflect atherogenic lipid burden compared to healthy controls in Sudanese adults?
Case-Control (n=490)
Yes
Does the Atherogenic Index of Plasma (AIP) accurately discriminate Type 2 Diabetes Mellitus status and independently reflect atherogenic lipid burden compared to healthy controls in Sudanese adults?
Sudanese adults with T2DM exhibit a substantially higher atherogenic lipid burden than healthy controls, and the Atherogenic Index of Plasma (AIP) serves as an accurate, low-cost, independent marker of this dyslipidemia distinct from glycemic metrics and adiposity.
Answers are grounded in this paper and cite their sources.
AIP may support dyslipidemia assessment in Sudanese T2DM; hypothesis-generating for diagnostic use pending prospective validation.
Background The atherogenic index of plasma (AIP) is an inexpensive composite marker of atherogenic lipid risk that has emerged as a valuable tool in patients with type 2 diabetes mellitus (T2DM), a population which cardiovascular risk is driven substantially by atherogenic dyslipidemia. However case–control data quantifying AIP performance in Sudanese adults with T2DM are lacking. Objective To quantify the burden of atherogenic dyslipidemia and evaluate the diagnostic and independent predictive performance of AIP in Sudanese adults with T2DM relative to healthy controls. Methods In this case control study, 245 adults with T2DM and 245 age- and sex-matched healthy controls were recruited from three teaching hospitals in Al Jazirah State, Sudan. Anthropometric indices and a fasting lipid and glycemic profile were measured, and AIP was calculated as log₁₀(triglycerides/HDL-cholesterol). Group differences were assessed with the Mann-Whitney U and Chi-square tests, associations with Spearman correlation, diagnostic performance with ROC curve analysis, and independent predictors with binary logistic regression adjusting for BMI, waist–hip ratio, and age. Results Cases showed a fully atherogenic lipid profile relative to controls, including significantly higher AIP (median 0.778 vs. 0.497, p < 0.001). Among cases, AIP correlated strongly with VLDL-C (r = 0.638, p < 0.001) but not with FBG, HbA1c, insulin, or HOMA-IR. AIP discriminated cases from controls with good accuracy (AUC = 0.821, 95% CI: 0.784–0.857; optimal cutoff 0.654, sensitivity 75.1%, specificity 73.5%) and remained an independent predictor of T2DM status after adjustment for BMI, waist–hip ratio, and age (Wald = 64.53, p < 0.001; overall model accuracy 87.6%). Conclusion Sudanese adults with T2DM carry a substantially greater atherogenic lipid burden than healthy controls, and AIP is an independent, low-cost marker of this risk that is distinct from glycemic status. AIP may serve as a practical adjunct for cardiovascular risk stratification in resource-limited settings.
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Siragalnoor et al. (2026) conducted a case-control in Type 2 diabetes mellitus and atherogenic dyslipidemia (n=490). Atherogenic index of plasma (AIP) / Type 2 diabetes mellitus vs. Healthy age- and sex-matched controls without diabetes was evaluated on Atherogenic index of plasma (AIP) discrimination of T2DM case status vs healthy controls (AUC 0.821, 95% CI 0.784-0.857, p=<0.001). Atherogenic index of plasma was higher in Sudanese T2DM cases than controls and discriminated T2DM status with an AUC of 0.821.
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