Whole-exome sequencing reveals Kawasaki disease susceptibility genes and their association with coronary artery lesion

被引:1
作者
Wang, Yazhou [1 ]
Chen, Xuepeng [1 ]
Zhang, Dufei [1 ]
Chen, Renwei [2 ]
Alifu, Ailixiati [2 ]
机构
[1] Hainan Women & Childrens Med Ctr, Dept Pediat Vasculocardiol, Haikou, Peoples R China
[2] Hainan Women & Childrens Med Ctr, Dept Cardiothorac Surg, Haikou, Peoples R China
基金
海南省自然科学基金;
关键词
Kawasaki disease; whole exome sequencing; coronary artery lesions; susceptibility genes; pediatrics; -; children; ENDOTHELIAL GROWTH-FACTOR; HUMAN-LEUKOCYTE ANTIGEN; CHILDREN; POLYMORPHISMS; ENDOSTATIN; DIAGNOSIS; VEGF;
D O I
10.3389/fped.2024.1400123
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objective This study aimed to explore Kawasaki disease (KD) susceptibility genes and their complications like coronary artery lesions (CAL) using whole exome sequencing (WES). Methods Between April 1, 2021, and December 31, 2022, our study included 55 pediatric patients diagnosed KD at our center, alongside a cohort of healthy children who sought medical care at our institution during the same timeframe. We extracted peripheral blood DNA from all participants and employed the advanced high-throughput Illumina Next-Generation Sequencing technology for comprehensive analysis. Through bioinformatics evaluation, we identified potential susceptibility genes. Moreover, from the 55 KD patients, we selected 15 for the CAL group and 40 for the non-CAL group. We aimed to investigate whether there were significant differences in the allele frequencies of the targeted susceptibility genes between these subgroups, to explore the risk alleles associated with the development of CAL in KD. Results HLA-DRB1 rs17882084 and IL6ST rs781455079 genotypes and alleles differed significantly between KD and non-KD (P < 0.05). No differences existed for IL17RC rs143781415 and VEGFB rs776229557 (P > 0.05). No differences in HLA-DRB1 rs17882084, IL6ST rs781455079, and VEGFB rs776229557 genotypes existed between CAL and non-CAL groups (P > 0.05). However, the IL17RC rs143781415 genotype differed significantly between them (P < 0.05). Conclusions HLA-DRB1 rs17882084 and IL6ST rs781455079 genotypes may be potential KD susceptibility gene candidates. Specifically, HLA-DRB1 rs17882084 GA genotype and A allele, and IL6ST rs781455079 TC genotype and C allele may increase KD risk. Additionally, the IL17RC rs143781415 genotype may increase CAL risk in KD patients.
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页数:7
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共 28 条
[1]   IL-17 Signaling: The Yin and the Yang [J].
Amatya, Nilesh ;
Garg, Abhishek V. ;
Gaffen, Sarah L. .
TRENDS IN IMMUNOLOGY, 2017, 38 (05) :310-322
[2]   Role of the PTEN/PI3K/VEGF pathway in the development of Kawasaki disease [J].
An, Xinjiang ;
Lv, Haitao ;
Tian, Jing ;
He, Xiuhua ;
Ling, Nan .
EXPERIMENTAL AND THERAPEUTIC MEDICINE, 2016, 11 (04) :1318-1322
[3]   VEGF in Signaling and Disease: Beyond Discovery and Development [J].
Apte, Rajendra S. ;
Chen, Daniel S. ;
Ferrara, Napoleone .
CELL, 2019, 176 (06) :1248-1264
[4]   Pro-inflammatory cytokine single nucleotide polymorphisms in Kawasaki disease [J].
Assari, Raheleh ;
Aghighi, Yahya ;
Ziaee, Vahid ;
Sadr, Maryam ;
Rahmani, Farzaneh ;
Rezaei, Arezou ;
Sadr, Zeinab ;
Moradinejad, Mohammad Hassan ;
Raeeskarami, Seyed Reza ;
Rezaei, Nima .
INTERNATIONAL JOURNAL OF RHEUMATIC DISEASES, 2018, 21 (05) :1120-1126
[5]   Neutrophil-Lymphocyte Ratio for Predicting Coronary Artery Lesions in Children With Kawasaki Disease [J].
Chidambaram, Aakash Chandran ;
Ramamoorthy, Jaikumar Govindaswamy ;
Anantharaj, Avinash .
INDIAN PEDIATRICS, 2023, 60 (03) :207-211
[6]   Genetic diagnosis by whole exome capture and massively parallel DNA sequencing [J].
Choi, Murim ;
Scholl, Ute I. ;
Ji, Weizhen ;
Liu, Tiewen ;
Tikhonova, Irina R. ;
Zumbo, Paul ;
Nayir, Ahmet ;
Bakkaloglu, Aysin ;
Ozen, Seza ;
Sanjad, Sami ;
Nelson-Williams, Carol ;
Farhi, Anita ;
Mane, Shrikant ;
Lifton, Richard P. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (45) :19096-19101
[7]   Th17-and Treg-related cytokine and mRNA expression are associated with acute and resolving Kawasaki disease [J].
Guo, M. M. -H. ;
Tseng, W. -N. ;
Ko, C. -H. ;
Pan, H. -M. ;
Hsieh, K. -S. ;
Kuo, H. -C. .
ALLERGY, 2015, 70 (03) :310-318
[8]   Kawasaki disease [J].
Harnden, Anthony ;
Takahashi, Masato ;
Burgner, David .
BRITISH MEDICAL JOURNAL, 2009, 338 :1133-1138
[9]   Genetic variations of HLA-DRB1 and susceptibility to Kawasaki disease in Taiwanese children [J].
Huang, Fu-Yuan ;
Chang, Tzu-Yang ;
Chen, Ming-Ren ;
Hsu, Chyong-Hsin ;
Lee, Hung-Chang ;
Lin, Shuan-Pei ;
Kao, Hsin-An ;
Chiu, Nan-Chang ;
Chi, Hsin ;
Liu, Tiffany Yi-Chen ;
Liu, Hsin-Fu ;
Dang, Ching-Wen ;
Chu, Chen-ng Chu ;
Lin, Marie ;
Sung, Tseng-Chen ;
Lee, Yann-Jinn .
HUMAN IMMUNOLOGY, 2007, 68 (01) :69-74
[10]   Association of vascular endothelial growth factor (VEGF) and VEGF receptor gene polymorphisms with coronary artery lesions of Kawasaki disease [J].
Kariyazono, H ;
Ohno, T ;
Khajoee, V ;
Ihara, K ;
Kusuhara, K ;
Kinukawa, N ;
Mizuno, Y ;
Hara, T .
PEDIATRIC RESEARCH, 2004, 56 (06) :953-959