Department of Hepatobiliary Surgery, Hebei General Hospital, Shijiazhuang, China.
Department of Ophthalmology, Tangdu Hospital, The Air Force Military Medical University, Xi'an, China.
Front Endocrinol (Lausanne). 2024 Sep 30;15:1415474. doi: 10.3389/fendo.2024.1415474. eCollection 2024.
Pancreatitis is a serious and complex inflammatory disease that imposes a severe effect on quality of life. Links between plasma lipidome and pancreatitis have been reported, some of which have not yet been clearly elucidated.
Therefore, our study aimed to investigate the causal relationships between plasma lipidome and four types of pancreatitis by conducting a bidirectional, two-sample Mendelian randomization (MR) analysis. We obtained genetic variants associated with 179 lipid species from a Genome-wide association analysis of plasma lipidome. The aggregated statistical data of acute pancreatitis (AP), alcohol-induced acute pancreatitis (AAP), chronic pancreatitis (CP), and alcohol-induced chronic pancreatitis (ACP) from the FinnGen consortium were exploited as the outcome. The inverse variance weighted (IVW) technique as the main method was used for MR analysis and sensitivity analyses were used to evaluate heterogeneity and pleiotropy.
After FDR correction, SE (27:1/20:4) (OR = 0.938, 95%CI = 0.906-0.972, P = 4.38 × 10, PFDR = 0.039) was identified to be significantly associated with AP risk. Eight lipid species were identified to be significantly associated with CP risk: SE (27:1/20:4) (OR = 0.911, 95%CI = 0.869-0.954, P = 8.89 × 10, PFDR = 0.016), LPC (20:4) (OR = 0.892, 95%CI = 0.843-0.945, P = 9.74 × 10, PFDR = 0.009), PC (16:0_22:5) (OR = 0.880, 95%CI = 0.818-0.947, P = 6.29 × 10, PFDR = 0.028), PC (17:0_20:4) (OR = 0.893, 95%CI = 0.842-0.948, P = 1.76 × 10, PFDR = 0.010), PC (18:0_20:4) (OR = 0.920, 95%CI = 0.874-0.969, P = 1.70 × 10, PFDR = 0.038), PC (O-16:0/20:4) (OR = 0.871, 95%CI = 0.804-0.943, P = 6.95 × 10, PFDR = 0.025), PC (O-16:1/20:4) (OR = 0.890, 95%CI = 0.832-0.953, P = 7.85 × 10, PFDR = 0.023), and PE (O-18:1/20:4) (OR = 0.866, 95%CI = 0.791-0.947, P = 1.61 × 10, PFDR = 0.041). Furthermore, genetically predicted increased LPC (20:4) (OR = 0.862, 95%CI = 0.796-0.934, P = 3.00 × 10, PFDR = 0.027) and SM (34:2;O2) (OR = 0.753, 95%CI = 0.659-0.860, P = 2.97 × 10, PFDR = 0.005) levels were associated with decreased risk of ACP.
Our findings provide evidence of causal associations between the specific types of lipidome and pancreatitis, offering new insights into future clinical research.
胰腺炎是一种严重且复杂的炎症性疾病,对生活质量造成严重影响。已经报道了血浆脂质组与胰腺炎之间的联系,其中一些尚未得到明确阐明。
因此,我们的研究旨在通过进行双向、两样本孟德尔随机化(MR)分析来研究血浆脂质组与四种类型胰腺炎之间的因果关系。我们从血浆脂质组的全基因组关联分析中获得了与 179 种脂质种类相关的遗传变异。利用 FinnGen 联盟的急性胰腺炎(AP)、酒精性急性胰腺炎(AAP)、慢性胰腺炎(CP)和酒精性慢性胰腺炎(ACP)的汇总统计数据作为结果。主要方法是使用逆方差加权(IVW)技术进行 MR 分析,并使用敏感性分析来评估异质性和多效性。
经过 FDR 校正,SE(27:1/20:4)(OR=0.938,95%CI=0.906-0.972,P=4.38×10,PFDR=0.039)与 AP 风险显著相关。有 8 种脂质种类与 CP 风险显著相关:SE(27:1/20:4)(OR=0.911,95%CI=0.869-0.954,P=8.89×10,PFDR=0.016),LPC(20:4)(OR=0.892,95%CI=0.843-0.945,P=9.74×10,PFDR=0.009),PC(16:0_22:5)(OR=0.880,95%CI=0.818-0.947,P=6.29×10,PFDR=0.028),PC(17:0_20:4)(OR=0.893,95%CI=0.842-0.948,P=1.76×10,PFDR=0.010),PC(18:0_20:4)(OR=0.920,95%CI=0.874-0.969,P=1.70×10,PFDR=0.038),PC(O-16:0/20:4)(OR=0.871,95%CI=0.804-0.943,P=6.95×10,PFDR=0.025),PC(O-16:1/20:4)(OR=0.890,95%CI=0.832-0.953,P=7.85×10,PFDR=0.023),PE(O-18:1/20:4)(OR=0.866,95%CI=0.791-0.947,P=1.61×10,PFDR=0.041)。此外,预测的 LPC(20:4)(OR=0.862,95%CI=0.796-0.934,P=3.00×10,PFDR=0.027)和 SM(34:2;O2)(OR=0.753,95%CI=0.659-0.860,P=2.97×10,PFDR=0.005)水平升高与 ACP 风险降低相关。
我们的研究结果提供了特定类型的脂质组与胰腺炎之间因果关系的证据,为未来的临床研究提供了新的见解。