医学
优势比
四分位数
赖氨酸
内科学
逻辑回归
哌啶酸
胃肠病学
置信区间
内分泌学
生物化学
氨基酸
生物
作者
Zihan Yin,Peicong Ge,Chaofan Zeng,Chenglong Liu,Yahui Zhao,Qihang Zhang,Hutao Xie,R. Matthew Brothers,Xingju Liu,Shuai Kang,Qian Zhang,Yan Zhang,Dong Zhang,Jizong Zhao
标识
DOI:10.1016/j.clnu.2023.12.021
摘要
Background and objective Lysine and its pathway metabolites have been identified as novel biomarkers for metabolic and vascular diseases. The role of them in the identification of moyamoya disease (MMD) has not been elucidated. This study aimed to determine the association between lysine pathway metabolites and the presence of MMD. Methods We prospectively enrolled 360 MMD patients and 89 healthy controls from September 2020 to December 2021 in Beijing Tiantan Hospital. Serum levels of lysine, pipecolic acid and 2-aminoadipic acid were measured by liquid chromatography-mass spectrometry. We employed logistic regression and restricted cubic spline to explore the association between these metabolites and the presence of MMD. Stratified analyses were also conducted to test the robustness of results. Results We observed that lysine levels in MMD patients were significantly higher and pipecolic acid levels were significantly lower compared to HCs (both p < 0.001), while no difference was found in the level of 2-AAA between both groups. When comparing metabolites by quartiles, elevated lysine levels were linked to increased odds for MMD (the fourth quartile [Q4] vs the first quartile [Q1]: odds ratio, 3.48, 95%CI [1.39–8.75]), while reduced pipecolic acid levels correlated with higher odds (Q4 vs Q1: odds ratio, 0.08; 95 % CI [0.03–0.20]). The restricted cubic spline found a L-shaped relationship between pipecolic acid level and the presence of MMD, with a cutoff point at 2.52 μmol/L. Robust results were also observed across subgroups. Conclusion Elevated lysine levels were correlated with increased odds of MMD presence, while lower pipecolic acid levels were associated with higher odds of the condition. These results suggest potential new biomarkers for the identification of MMD. Clinical trial registry number URL: https://www.chictr.org.cn/. Unique identifier: ChiCTR2200061889.
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