Key result
Higher WBC count is linked to ~41% increased odds of insulin resistance in non-obese adults.
Why the study?
Are inflammatory markers associated with insulin resistance in non-obese adults across different BMI strata?
Cross-Sectional (n=149)
No
Are inflammatory markers associated with insulin resistance in non-obese adults across different BMI strata?
Odds Ratio: 1.407 (95% CI 1.09–1.815)
p-value: p=0.009
Different inflammatory markers predict insulin resistance across BMI strata in non-obese adults, with WBC count relevant for normal-weight and CRP/HDL ratio for overweight individuals.
Background Insulin resistance (IR) is a key mechanism underlying type 2 diabetes mellitus and cardiometabolic disease. Although obesity-related inflammation is a major contributor to IR, increasing evidence indicates that IR may also develop in non-obese individuals. However, readily available inflammatory markers applicable to this population remain limited. We evaluated the association between inflammatory markers and insulin resistance in non-obese adults and assessed their predictive performance across body mass index (BMI) strata. Methods This retrospective cross-sectional study included 149 non-obese adults (BMI < 30 kg/m 2 ) evaluated in an internal medicine outpatient clinic between January and December 2025. Insulin resistance was defined as a homeostasis model assessment of insulin resistance (HOMA-IR) ≥ 2.5. Inflammatory markers and composite indices, including the C-reactive protein to high-density lipoprotein cholesterol (CRP/HDL) ratio, were calculated. Multivariable logistic regression, BMI-stratified analyses, and receiver operating characteristic (ROC) curve analyses were performed. Results Insulin resistance was identified in 54 participants (36.2%). Individuals with IR had higher white blood cell (WBC) counts, CRP levels, and CRP/HDL ratios (all p < 0.05). In multivariable analysis, WBC count was independently associated with IR (OR = 1.407, 95% CI [1.090–1.815]; p = 0.009). BMI-stratified analyses showed that WBC count independently predicted IR in normal-weight individuals (OR = 1.789, 95% CI [1.218–2.627]; p = 0.003), whereas in overweight participants (BMI 25–30 kg/m 2 ), the CRP/HDL ratio was independently associated with IR (OR = 7.793, 95% CI [1.056–57.499]; p = 0.044). ROC analyses demonstrated higher discriminative performance of WBC count in normal-weight individuals (AUC = 0.720) and greater predictive ability of the CRP/HDL ratio in overweight individuals (AUC = 0.695). Conclusions Low-grade systemic inflammation is independently associated with insulin resistance in non-obese adults, with distinct inflammatory predictors across BMI categories. WBC count may reflect early immune activation in normal-weight individuals, whereas the CRP/HDL ratio appears more informative among overweight subjects.
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Acet et al. (2026) conducted a cross-sectional in Insulin resistance (n=149). White blood cell count and CRP/HDL ratio was evaluated on Insulin resistance (HOMA-IR ≥ 2.5) (OR 1.407, 95% CI 1.090-1.815, p=0.009). Higher white blood cell count was independently associated with insulin resistance in non-obese adults (OR 1.407; 95% CI 1.090-1.815; P=0.009), with CRP/HDL ratio highly predictive in overweight subjects.
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