An untargeted serum and urine lipidomics research based on UPLC–MS revealed the lipid alterations on adjuvant‐induced arthritis rats

脂类学 脂质代谢 脂质体 化学 代谢组学 新陈代谢 尿 脂肪酸代谢 色谱法 生物化学
作者
Wei Shi,Yue Han
出处
期刊:Biomedical Chromatography [Wiley]
卷期号:37 (11) 被引量:2
标识
DOI:10.1002/bmc.5736
摘要

Rheumatoid arthritis (RA) is a systemic autoimmune disease dominated by chronic inflammatory lesions of peripheral synovial joints. Growing evidence suggests that abnormal lipid metabolism levels contribute to the progression of RA. Although several metabolomics studies have shown abnormality in the RA lipidome, the relationship between the overall lipid metabolites and RA has not been systematically evaluated. In this study, an untargeted lipidomics method based on ultra performance liquid chromatography-mass spectrometry (UPLC-MS) was used to analyze the serum and urine lipidomes of adjuvant-induced arthritis rats to study the characteristics of lipid metabolism changes in the rats and search lipid markers for diagnosing RA. By combining with orthogonal partial least squares discriminant analysis, a total of 52 potential lipid markers were identified, mainly involved in sphingolipid metabolism, glycerophospholipid metabolism, sterol lipid metabolism, glycerolipid metabolism and fatty acid metabolism, which provided crucial insight into lipid metabolism disturbances in RA. Further receiver operating characteristic analysis revealed that the areas under the curve of PC(22:4/16:0), PI(18:1/16:0) and LacCer(d18:1/12:0) from serum and 25-hydroxycholesterol from urine were 0.94, 1.00, 1.00 and 1.00, respectively, indicating the high predictive ability of this method for RA. In this study, our results indicated that a combination of serum and urine analysis can provide a more comprehensive and reliable assessment of RA, and a UPLC-MS-based lipidomics strategy is a powerful tool to search for potential lipid markers associated with RA and explore the pathogenesis of RA.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
英俊的铭应助Romy211采纳,获得10
刚刚
1秒前
研友_VZG7GZ应助阿航采纳,获得10
1秒前
2秒前
HUAJIAO完成签到,获得积分10
3秒前
李李李李李完成签到,获得积分10
4秒前
fancy完成签到,获得积分10
4秒前
4秒前
SYLH应助Tracy麦子采纳,获得10
4秒前
liu发布了新的文献求助10
5秒前
Atlantis发布了新的文献求助10
6秒前
咕咕咕完成签到,获得积分20
7秒前
7秒前
啊啊啊橙子完成签到,获得积分10
8秒前
李爱国应助jingtan采纳,获得10
8秒前
初初见你完成签到 ,获得积分10
8秒前
11秒前
你吃饱了吗完成签到,获得积分20
11秒前
Masaccy完成签到,获得积分10
11秒前
柯一一应助www采纳,获得10
12秒前
hyd发布了新的文献求助10
12秒前
打打应助华北走地鸡采纳,获得10
14秒前
15秒前
CodeCraft应助未来可期采纳,获得10
15秒前
yznfly应助活泼烤鸡采纳,获得20
15秒前
吴大打完成签到,获得积分10
16秒前
16秒前
海贼学术完成签到,获得积分10
16秒前
李爱国应助luogan采纳,获得10
16秒前
17秒前
FashionBoy应助55555555采纳,获得10
18秒前
舒适的蓝天完成签到,获得积分20
18秒前
LSH970829发布了新的文献求助10
19秒前
20秒前
龙梦发布了新的文献求助10
20秒前
20秒前
江阳宏发布了新的文献求助10
22秒前
852应助LY学生采纳,获得10
22秒前
jingtan发布了新的文献求助10
25秒前
高分求助中
ФОРМИРОВАНИЕ АО "МЕЖДУНАРОДНАЯ КНИГА" КАК ВАЖНЕЙШЕЙ СИСТЕМЫ ОТЕЧЕСТВЕННОГО КНИГОРАСПРОСТРАНЕНИЯ 3000
Electron microscopy study of magnesium hydride (MgH2) for Hydrogen Storage 1000
生物降解型栓塞微球市场(按产品类型、应用和最终用户)- 2030 年全球预测 500
Quantum Computing for Quantum Chemistry 500
Thermal Expansion of Solids (CINDAS Data Series on Material Properties, v. I-4) 470
Fire Protection Handbook, 21st Edition volume1和volume2 360
Phylogenetic study of the order Polydesmida (Myriapoda: Diplopoda) 360
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3902656
求助须知:如何正确求助?哪些是违规求助? 3447386
关于积分的说明 10849014
捐赠科研通 3172725
什么是DOI,文献DOI怎么找? 1753080
邀请新用户注册赠送积分活动 847544
科研通“疑难数据库(出版商)”最低求助积分说明 790067