Journal of Developmental Medicine(Electronic Version)   2024, Vol. 12   Issue (6): 415-421    DOI: 10.3969/j.issn.2095-5340.2024.06.002 | 
										 
				   
				
					
						
							
								
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    					| Mendelian randomization analysis on the causal relationship between systemic lupus erythematosus and preeclampsia | 
  					 
  					  										
						| Gui Qi, Hou Wei, Hu Jialin, et al
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						(1. Chinese PLA Medical School,Beijing 100853, China; 2. Medical of School, Nankai University, Tianjin 300071, China; 3. Department ofObstetrics and Gynecology, the First Medical Center of Chinese PLA General Hospital, Beijing 100853,China; 4. Department of Obstetrics and Gynecology, the Seventh Medical Center of Chinese PLA General Hospital, Beijing 100700, China)
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													     		                            						                            																	    Abstract  【Abstract】 Objective To investigate the causal relationship between systemic lupus erythematosus (SLE)and preeclampsia (PE). Method Utilizing the R package TwoSampleMR (0.6.4), single nucleotide 
polymorphism (SNP) significantly associated with SLE were screened from the IEU OpenGWAS 
database and used as instrumental variables. A dataset containing 7 071 163 SNP for SLE and another 
with 24 165 538 SNP for PE were obtained. Mendelian randomization (MR) analysis were conducted 
using inverse-variance weighting (IVW), MR-Egger regression, the weighted median estimator (WME), 
simple mode (SM), and weighted mode (WM). The causal relationship between SLE and PE was evaluated 
by calculating odds ratios (OR) and 95% CI. Cochran's Q test for heterogeneity, MR-Egger horizontal pleiotropytest and leave-one-out analysis were performed to assess the stability and reliability of the data. Result Atotal of 42 SNP were included as instrumental variables. The IVW analysis suggested a causal relationshipbetween SLE and the risk of PE (OR=1.038, 95% CI: 1.003-1.073, P<0.05). Consistent results were alsoobtained from the MR-Egger regression analysis (OR=1.094, 95% CI: 1.020-1.174, P<0.05). However, nocausal relationship was found between SLE and PE in the WME, SM, and WM analysis. Cochran's Q test forheterogeneity and MR-Egger horizontal pleiotropy test indicated no heterogeneity or horizontal pleiotropyamong the SNP. The leave-one-out analysis suggested that no single SNP had a significant impact on the overall results. Conclusion MR analysis suggests that SLE may increase the risk of developing PE. 
 
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															    																	Received: 26 August 2024
																	    
															    															    															    																	Published: 27 November 2024
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