Center of Reproductive Medicine, Shengjing Hospital of China Medical University, Shenyang, China.
NHC Key Laboratory of Advanced Reproductive Medicine and Fertility (China Medical University), National Health Commission, Shenyang, China.
Hum Reprod. 2024 Nov 1;39(11):2575-2586. doi: 10.1093/humrep/deae219.
Is there a relationship between serum uric acid and fructose levels in polycystic ovary syndrome (PCOS)?
Elevated serum uric acid levels in women with PCOS positively correlate with serum fructose levels, and elevated serum fructose levels are an independent risk factor for hyperuricemia in women with PCOS.
Our previous study suggested a link between elevated serum fructose levels and PCOS. Fructose is unique as it generates uric acid during metabolism, and high uric acid levels are associated with metabolic disorders and an increased risk of anovulation. However, the relationship between serum uric acid and fructose levels in women with PCOS remains unclear.
STUDY DESIGN, SIZE, DURATION: In a case-control study of 774 women (482 controls and 292 patients with PCOS) between May and October 2020 at the Shengjing Hospital of China Medical University, the relationship between uric acid and fructose levels in women with PCOS was examined. Participants were divided into subgroups based on various factors, including BMI, insulin resistance, dyslipidemia, metabolic syndrome, and hyperuricemia.
PARTICIPANTS/MATERIALS, SETTING, METHODS: Serum uric acid concentrations were measured using enzymatic assays, and serum fructose levels were determined using a fluorescent enzyme immunoassay. Dietary fructose data were collected through a validated food-frequency questionnaire of 81 food items. We applied restricted cubic splines to a flexibly model and visualized the linear/nonlinear relationships between serum uric acid and fructose levels in PCOS. Multivariate logistic analysis was executed to assess the association between serum fructose levels and hyperuricemia in PCOS. Human granulosa cell and oocyte mRNA profile sequencing data were downloaded for mapping uric acid and fructose metabolism genes in PCOS. Further downstream analyses, including Gene Ontology, Kyoto Encyclopedia of Genes and Genomes analysis, and protein-protein interactions were then carried out on the differentially expressed genes (DEGs). The correlation between uric acid and fructose metabolism genes was calculated using the Pearson correlation coefficient. The GeneCards database was used to identify DEGs related to uric acid and fructose metabolism in PCOS, and then several DEGs were confirmed by quantitative real-time PCR.
Both serum fructose and uric acid levels were significantly increased in women with PCOS compared with the control women (P < 0.001), and there was no statistically significant difference in dietary fructose intake between PCOS and controls, regardless of metabolic status. There was a positive linear correlation between serum uric acid and fructose levels in women with PCOS (Poverall < 0.001, Pnon-linear = 0.30). In contrast, no correlation was found in control women (Poverall = 0.712, Pnon-linear = 0.43). Additionally, a non-linear association was observed in the obese subgroup of patients with PCOS (Poverall < 0.001, Pnon-linear = 0.02). Serum uric acid levels were linearly and positively associated with serum fructose levels in patients with PCOS with insulin resistance, dyslipidemia, and metabolic syndrome. Furthermore, even after adjusting for confounding factors, elevated serum fructose levels were an independent risk factor for hyperuricemia in patients with PCOS (P = 0.001; OR, 1.380; 95% CI, 1.207-1.577). There were 28 uric acid and 25 fructose metabolism genes which showed a significant correlation in PCOS. Seven upregulated genes (CAT, CRP, CCL2, TNF, MMP9, GCG, and APOB) related to uric acid and fructose metabolism in PCOS ovarian granulosa cells were ultimately successfully validated using quantitative real-time PCR.
LIMITATIONS, REASONS FOR CAUTION: Due to limited conditions, more possible covariates (such as smoking and ethnicity) were not included, and the underlying molecular mechanism between fructose and uric acid levels in women with PCOS remains to be further investigated.
The results of this study and our previous research indicate that the high uric acid status of PCOS may be mediated by fructose metabolism disorders, highlighting the importance of analyzing fructose metabolism, and especially its metabolic byproduct uric acid, during the clinical diagnosis of PCOS. These results suggest the adverse effects of high uric acid in PCOS, and the importance of taking early interventions regarding uric acid levels to reduce the occurrence and development of further clinical signs, such as metabolic disorders in women with PCOS.
STUDY FUNDING/COMPETING INTEREST(S): This work was supported by: the National Natural Science Foundation of China (No. 82371647, No. 82071607, and No. 32100691); LiaoNing Revitalization Talents Program (No. XLYC1907071); Fok Ying Tung Education Foundation (No. 151039); and Outstanding Scientific Fund of Shengjing Hospital (No. 202003). No competing interests were declared.
N/A.
多囊卵巢综合征(PCOS)患者血清尿酸和果糖水平之间是否存在关系?
PCOS 女性的血清尿酸水平升高与血清果糖水平呈正相关,而血清果糖水平升高是 PCOS 女性高尿酸血症的独立危险因素。
我们之前的研究表明,升高的血清果糖水平与 PCOS 之间存在关联。果糖是独特的,因为它在代谢过程中产生尿酸,而高尿酸水平与代谢紊乱和无排卵风险增加有关。然而,PCOS 女性血清尿酸和果糖水平之间的关系仍不清楚。
研究设计、规模、持续时间:2020 年 5 月至 10 月,在中国医科大学盛京医院对 774 名女性(482 名对照和 292 名 PCOS 患者)进行病例对照研究,研究了 PCOS 女性尿酸和果糖水平之间的关系。参与者根据 BMI、胰岛素抵抗、血脂异常、代谢综合征和高尿酸血症等各种因素分为亚组。
参与者/材料、设置、方法:使用酶法测定血清尿酸浓度,使用荧光酶免疫测定法测定血清果糖水平。通过经过验证的 81 种食物的食物频率问卷收集膳食果糖数据。我们应用受限立方样条对模型进行灵活建模,并可视化 PCOS 中血清尿酸和果糖水平之间的线性/非线性关系。使用多元逻辑回归分析评估血清果糖水平与 PCOS 中高尿酸血症的关系。下载人颗粒细胞和卵母细胞 mRNA 谱测序数据,以映射 PCOS 中尿酸和果糖代谢基因。然后对差异表达基因(DEGs)进行基因本体论、京都基因与基因组百科全书分析和蛋白质-蛋白质相互作用的下游分析。使用 Pearson 相关系数计算尿酸和果糖代谢基因之间的相关性。使用 GeneCards 数据库鉴定与 PCOS 中尿酸和果糖代谢相关的 DEGs,然后通过定量实时 PCR 确认几个 DEGs。
与对照组女性相比,PCOS 女性的血清果糖和尿酸水平均显著升高(P<0.001),无论代谢状态如何,PCOS 和对照组之间的膳食果糖摄入量均无统计学差异。在 PCOS 女性中,血清尿酸和果糖水平之间存在正线性相关(Poverall<0.001,Pnon-linear=0.30)。相比之下,在对照组女性中未发现相关性(Poverall=0.712,Pnon-linear=0.43)。此外,在肥胖的 PCOS 患者亚组中观察到非线性关联(Poverall<0.001,Pnon-linear=0.02)。在伴有胰岛素抵抗、血脂异常和代谢综合征的 PCOS 患者中,血清尿酸水平与血清果糖水平呈线性正相关。此外,即使在调整混杂因素后,升高的血清果糖水平仍是 PCOS 患者高尿酸血症的独立危险因素(P=0.001;OR,1.380;95%CI,1.207-1.577)。在 PCOS 中,有 28 个尿酸代谢基因和 25 个果糖代谢基因显示出显著相关性。最终使用定量实时 PCR 成功验证了 7 个与 PCOS 卵巢颗粒细胞中尿酸和果糖代谢相关的上调基因(CAT、CRP、CCL2、TNF、MMP9、GCG 和 APOB)。
局限性、谨慎的原因:由于条件有限,更多可能的混杂因素(如吸烟和种族)未被纳入,PCOS 女性中果糖和尿酸水平之间的潜在分子机制仍有待进一步研究。
本研究和我们之前的研究结果表明,PCOS 的高尿酸血症状态可能是由果糖代谢紊乱介导的,这强调了在 PCOS 的临床诊断中分析果糖代谢,特别是其代谢产物尿酸的重要性。这些结果提示了 PCOS 中高尿酸血症的不良影响,以及采取早期干预尿酸水平的重要性,以降低女性 PCOS 进一步发生临床体征的风险,如代谢紊乱。
研究资金/利益冲突:这项工作得到了以下支持:国家自然科学基金(No. 82371647、No. 82071607 和 No. 32100691);辽宁省振兴人才计划(No. XLYC1907071);福英东教育基金会(No. 151039);和盛京医院杰出科学基金(No. 202003)。没有竞争利益的声明。
无。