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Study 30 of 33Erythropoietin (EPO) literatureRenal failure · Observational2026

The relationship between the non-high-density lipoprotein cholesterol to high-density lipoprotein cholesterol ratio and tubular atrophy/interstitial fibrosis in patients with IgA nephropathy.

Elevated NHHR is associated with an increased risk of tubular atrophy/interstitial fibrosis in patients with IgA nephropathy, but the clinical implications of this finding need further investigation.

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this study against the rest of the erythropoietin (epo) corpus
5
Preclinical
21
Observational · this one
1
Open-label
2
Randomised
4
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Summary and findings

This study examined the relationship between the non-high-density lipoprotein cholesterol to high-density lipoprotein cholesterol ratio (NHHR) and tubular atrophy/interstitial fibrosis (T) lesions in 400 patients with biopsy-proven IgA nephropathy (IgAN). The highest NHHR quartile showed significantly adverse clinical profiles and a higher prevalence of T1/T2 lesions. NHHR was positively correlated with T lesions.

How much of this paper we could read: full text read (0.90). We had a clear abstract, so the summary below closely tracks the paper. What this means →
NHHR was positively correlated with T lesions (r = 0.229, p < 0.001).n=4002026

Abstract

The authors’ words, as Renal failure supplied them

<b>Background:</b> The tubular atrophy/interstitial fibrosis (T) lesions of the Oxford Classification is a key prognostic determinant in IgA nephropathy (IgAN). The non-high-density lipoprotein cholesterol to high-density lipoprotein cholesterol ratio (NHHR) is an emerging lipid marker, but its link with renal histologic damage in IgAN is unknown.<b>Methods:</b> This cross-sectional and retrospective study investigated the relationship between NHHR and T lesions in 400 biopsy-proven IgAN patients. Participants were divided into NHHR quartiles. The association between NHHR and T lesions was assessed using Spearman's rank correlation analysis, binary logistic regression analysis, restricted cubic spline (RCS) analysis, receiver operating characteristic (ROC) curve analysis, and subgroup analysis.<b>Results:</b> Compared to the lowest quartile (Q1), the highest NHHR quartile (Q4) showed significantly adverse clinical profiles and a higher prevalence of T1/T2 lesions (<i>p</i> < 0.05). NHHR was positively correlated with T lesions (<i>r</i> = 0.229, <i>p</i> < 0.001). Multivariate logistic regression analysis identified elevated NHHR and reduced estimated glomerular filtration rate (eGFR) as independent risk factors for T1/T2 lesions. RCS analysis demonstrated a linear association between NHHR and the risk of T1/T2 lesions (<i>p</i> for nonlinearity = 0.343). The ROC curve analysis yielded an area under the curve (AUC) of 0.635 for NHHR alone (optimal cutoff value = 3.54, sensitivity = 58.2%, specificity = 63.6%), and the composite NHHR+eGFR model achieved an AUC of 0.814. Subgroup analysis showed a consistent association between NHHR and the risk of T1/T2 lesions across all subgroups, with no significant interaction effects.<b>Conclusion:</b> Elevated NHHR is an independent risk factor for the progression of T lesions in patients with IgAN.

Background

This paper addresses the relationship between NHHR and renal histologic damage in IgA nephropathy (IgAN), a condition where tubular atrophy and interstitial fibrosis are key prognostic determinants. Prior studies have not established a link between NHHR and T lesions in IgAN, making this investigation relevant for understanding potential risk factors for disease progression. The findings could have implications for risk stratification in patients with IgAN.

Methods

This cross-sectional and retrospective study included 400 biopsy-proven IgAN patients. Participants were divided into NHHR quartiles, and the relationship between NHHR and T lesions was assessed using various statistical analyses including Spearman's rank correlation, binary logistic regression, and ROC curve analysis.

Results

The primary finding indicated that NHHR was positively correlated with T lesions (r = 0.229, p < 0.001). The highest NHHR quartile (Q4) showed significantly adverse clinical profiles and a higher prevalence of T1/T2 lesions compared to the lowest quartile (Q1) (p < 0.05). The ROC curve analysis yielded an AUC of 0.635 for NHHR alone, with an optimal cutoff value of 3.54, sensitivity of 58.2%, and specificity of 63.6%.

Interpretation

The study finds a statistically significant correlation between NHHR and T lesions, but the clinical significance of the effect size remains uncertain. While the AUC of 0.814 for the composite model suggests a better predictive capability, the findings are limited by the cross-sectional design and potential confounding factors. This implies that while NHHR may be a marker of risk, its practical utility in clinical settings requires further validation.

Key findings

  • NHHR was positively correlated with T lesions (r = 0.229, p < 0.001).
  • Compared to the lowest quartile (Q1), the highest NHHR quartile (Q4) showed significantly adverse clinical profiles and a higher prevalence of T1/T2 lesions (p < 0.05).
  • The ROC curve analysis yielded an area under the curve (AUC) of 0.635 for NHHR alone (optimal cutoff value = 3.54, sensitivity = 58.2%, specificity = 63.6%).
  • The composite NHHR+eGFR model achieved an AUC of 0.814.
  • Multivariate logistic regression identified elevated NHHR and reduced estimated glomerular filtration rate (eGFR) as independent risk factors for T1/T2 lesions.

Limitations

  • cross-sectional and retrospective design limits causal inferences
  • single biopsy assessment may not capture disease progression accurately
  • small sample size may limit generalizability

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