Zhou Wen, Xia Qingqing, Liu Duan, Li Jun-Ying, Gong Liang
Chengdu Second People's Hospital, Chengdu, Sichuan, China.
Front Neurosci. 2025 Mar 25;19:1555831. doi: 10.3389/fnins.2025.1555831. eCollection 2025.
The correlation between serum sodium and sporadic Parkinson's disease remains unclear currently. This study aimed to assess the association between serum sodium and sporadic Parkinson's disease.
The ultimate goal is to gain a deeper understanding of the implications of this relationship between serum sodium and sporadic Parkinson's disease.
We conducted a retrospective cross-sectional study involving 1,189 participants in PPMI cohort. Age, sex, education years, race, body mass index, calcium, alanine aminotransferase, aspartate aminotransferase, white blood cell, lymphocytes, neutrophils, monocytes, red blood cell, hemoglobin, platelets, total protein, albumin, serum uric acid, serum sodium, serum potassium, urea nitrogen, creatinine, serum glucose were obtained from all participants. Logistic regression, and smooth curve fitting were utilized to substantiate the research objectives.
The overall sporadic Parkinson's disease was 77.5% (921/1189); it was 71.9% (143/199), 75.4% (295/391), 76.7% (171/223), and 83% (312/376) for serum sodium quantile1 (Q1, 130-138.9 mmol/L), quantile 2 (Q2, 139-140.9 mmol/L), quantile 3 (Q3, 141-141.9 mmol/L), and quantile 4 (Q4, 142-155 mmol/L), respectively ( = 0.011). Multivariate odds ratio regression adjusted for risk factors demonstrates a 1-unit increment in the serum sodium raises the risk of sporadic Parkinson's disease by 1.11 times, respectively. Smooth splines analysis suggested a linear association between levels of serum sodium and risk of sporadic Parkinson's disease (P nonlinearity = 0.5). An interaction was observed between serum sodium and sex in their influence on sporadic Parkinson's disease ( < 0.05). Further exploratory subgroup analysis within the age and BMI groups showed that there were no significant interactions between the subgroups (all values for interaction were > 0.05). Additional sensitivity analyses supported the primary findings and indicated the conclusions are robust.
This study highlights the influence of inappropriate serum sodium on the risk of incident sporadic Parkinson's disease, independent of confounders. The link between serum sodium and sporadic Parkinson's disease is linear.
目前血清钠与散发性帕金森病之间的相关性尚不清楚。本研究旨在评估血清钠与散发性帕金森病之间的关联。
最终目的是更深入地了解血清钠与散发性帕金森病之间这种关系的意义。
我们对PPMI队列中的1189名参与者进行了一项回顾性横断面研究。获取了所有参与者的年龄、性别、受教育年限、种族、体重指数、钙、丙氨酸转氨酶、天冬氨酸转氨酶、白细胞、淋巴细胞、中性粒细胞、单核细胞、红细胞、血红蛋白、血小板、总蛋白、白蛋白、血清尿酸、血清钠、血清钾、尿素氮、肌酐、血糖。采用逻辑回归和平滑曲线拟合来证实研究目标。
散发性帕金森病总体患病率为77.5%(921/1189);血清钠四分位数1(Q1,130 - 138.9 mmol/L)、四分位数2(Q2,139 - 140.9 mmol/L)、四分位数3(Q3,141 - 141.9 mmol/L)和四分位数4(Q4,142 - 155 mmol/L)时的患病率分别为71.9%(143/199)、75.4%(295/391)、76.7%(171/223)和83%(312/376)(P = 0.011)。经风险因素调整的多变量优势比回归显示,血清钠每增加1个单位,散发性帕金森病的风险分别增加1.11倍。平滑样条分析表明血清钠水平与散发性帕金森病风险之间存在线性关联(P非线性 = 0.5)。观察到血清钠和性别在对散发性帕金森病的影响上存在交互作用(P < 0.05)。在年龄和体重指数组内进行的进一步探索性亚组分析表明,各亚组之间没有显著交互作用(所有交互作用的P值均> 0.05)。额外的敏感性分析支持了主要研究结果,并表明结论具有稳健性。
本研究强调了血清钠异常对散发性帕金森病发病风险的影响,独立于混杂因素。血清钠与散发性帕金森病之间的联系是线性的。