Abstract

BackgroundThe association between homocysteine (Hcy) and IgA nephropathy (IgAN) is not well understood. We aimed to investigate the relationship between Hcy and clinicopathologic features in IgAN patients.MethodsA total of 337 IgAN patients and 150 sex- and age- matched healthy controls were enrolled in this single-center retrospective study. According to Hcy ≤ 10 μmol/L or > 10 μmol/L, patients were divided into low and high Hcy groups. Multivariate logistic regression was performed to explore the risk factors for elevated Hcy.ResultsSerum Hcy was higher in IgAN patients than in healthy controls [11.6 (9.1,15.3) vs. 8.8 (7.5,10.6) μmol/L, P < 0.001], unanimously in the subgroup of 156 patients with a normal estimated glomerular filtration rate (eGFR) (≥ 90 ml/min/1.73 m2) [9.9 (7.6,12.4) vs. 8.8 (7.5,10.6) μmol/L, P < 0.001]. Compared to the low Hcy group, serum creatinine (Scr), blood urine nitrogen (BUN), uric acid (UA), endocapillary hypercellularity (E) and tubular atrophy/interstitial fibrosis lesion (T) were higher in the high Hcy group. Hcy levels were positively correlated with Scr, BUN, UA, 24-h urine protein, and E and T lesions, but negatively correlated with eGFR and superoxide dismutase (SOD). In the subgroup with normal eGFR, patients with higher Hcy were persistent with higher Scr, BUN and T lesions. A multivariate logistic regression model showed that the risk of elevated Hcy in patients with pathological T increased by 2.87-fold. T lesions could better predict high Hcy, with an odds ratio (OR) of 14.20 in the subgroup with normal eGFR.ConclusionsPathologic T was an independent risk factor associated with elevated Hcy, especially at the early stage of IgAN.

Highlights

  • The association between homocysteine (Hcy) and immunoglobulin A (IgA) nephropathy (IgAN) is not well understood

  • We investigated the relationship between Hcy and clinicopathologic characteristics in IgA nephropathy (IgAN) patients in our center, especially at an early stage with a normal estimated glomerular filtration rate (≥ 90 ml/min/1.73 ­m2)

  • Multivariate logistic regression analysis showed that pathologic T was an independent risk factor for elevated Hcy in IgAN patients and persisted in a subgroup analysis according to estimated glomerular filtration rate (eGFR) ≥90 ml/min/1.73 m­ 2

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Summary

Introduction

The association between homocysteine (Hcy) and IgA nephropathy (IgAN) is not well understood. We aimed to investigate the relationship between Hcy and clinicopathologic features in IgAN patients. Numerous studies have found that elevated serum Hcy is a nontraditional independent risk factor for cardiovascular disease (CVD) [2, 3]. A small retrospective study from Duan et al revealed that elevated Hcy was associated with poor renal outcome in IgAN patients [10]. Another study by Mendelian randomization (MR) analysis observed positive effects of Hcy on serum creatinine, blood pressure (BP), and pathogenic T lesions in IgAN patients [11]. Only the two small-sample studies mentioned above have investigated the relationship between Hcy and IgAN patients. Clinical research on the relationship between Hcy and pathology has not yet been highlighted

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