Abstract

Uric acid (UA) is a major antioxidant molecule in the human blood, and it has been linked with cell longevity. However, it is unclear whether serum UA levels are associated with red blood cell (RBC) indexes. This cross-sectional study included 10,759 Chinese subjects, recruited from the Shanghai Xuhui Central Hospital from January 2014 to December 2017. The participants were categorized into gender groups and then further divided into three different subgroups according to their UA reference range as follows: low (male (UA < 0.202 mmol/l), female (UA < 0.143 mmol/l)), normal (male (0.417 mmol/l > UA ≥ 0.202 mmol/l), female (0.339 mmol/l > UA ≥ 0.143 mmol/l)), and high (male (UA ≥ 0.417 mmol/l), female (UA ≥ 0.339 mmol/l)). The associations of UA levels with RBC parameters were analyzed using 1-way ANOVA, Pearson correlations, and multivariate linear regression. The levels of mean corpuscular hemoglobin, mean corpuscular hemoglobin concentration, RBCs, and hemoglobin were lowest in the low UA group, followed by the normal UA group and high UA group (p < 0.001). Pearson analysis showed that there was a statistically significant correlation between UA levels with mean corpuscular hemoglobin, mean corpuscular hemoglobin concentrations, mean corpuscular volumes, RBC counts, and hemoglobin (p < 0.05). Multiple linear regression analysis suggested that there were statistically significant positive correlations between UA levels and RBC counts (B = 0.245, p < 0.001, 95% CI = 0.003 to 0.092), as well as UA levels and hemoglobin concentrations (B = 0.138, p < 0.001, 95% CI = 0.002 to 0.082). Furthermore, similar results were observed in both the male and female subgroups. The serum UA levels may be independently associated with RBC parameters, regardless of sex, and UA may protect RBCs owing to its antioxidant effect.

Highlights

  • Uric acid (UA) oxidase, an enzyme that converts UA to 5hydroxy isourate and H2O2, was lost in hominoids during primate evolution

  • Based on the level of UA, the subjects were categorized into three subgroups: 494 subjects were classified as low UA, 8615 as normal UA, and 1650 as high UA group

  • In the female subgroup, this was true only of red blood cell (RBC) and hemoglobin levels, which were the lowest in the low UA group, followed by the normal UA group and the high UA group (p < 0 001); no correlation was found between RBC levels and mean corpuscular hemoglobin (MCH) or mean corpuscular hemoglobin concentration (MCHC) levels (Table 3, Figure 3)

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Summary

Introduction

Uric acid (UA) oxidase, an enzyme that converts UA to 5hydroxy isourate and H2O2, was lost in hominoids during primate evolution. This loss of UA oxidase may have evolutionary advantages [1, 2], as the average level of serum UA in human is 5- to over 20-fold higher than in most other mammals [1]. There has been increasing experimental and clinical evidence suggesting that higher plasma UA levels may protect humans from cancer, multiple sclerosis, central nervous system diseases, glaucoma, and other life-shortening disorders [10,11,12,13,14,15,16]. Recent evidence from an in vitro study has shown an intrinsic variability in plasma UA levels that might be related to the interdonor variability observed in the storage capacity of red blood cells (RBCs), and this has led to the proposal of a model for the Oxidative Medicine and Cellular Longevity

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