Abstract 15595: Whole Genome Sequencing to Identify Predictors of IVIG Response in Kawasaki Disease

医学 单核苷酸多态性 SNP公司 逻辑回归 全基因组测序 基因 川崎病 内科学 遗传学 基因组 基因型 生物 动脉
作者
Sadeep Shrestha,Howard W. Wiener,Hidemi Kajimoto,Vinodh Srinivasasainagendra,Dolena R. Ledee,Sabrina Chowdhury,Mikayla A. Beckley,Luz A. Padilla,Nagib Dahdah,Hemant K. Tiwari,Michael A. Portman
出处
期刊:Circulation [Lippincott Williams & Wilkins]
卷期号:146 (Suppl_1) 被引量:1
标识
DOI:10.1161/circ.146.suppl_1.15595
摘要

Introduction: Kawasaki Disease (KD) leads as a cause of acquired cardiovascular disease among children in developed countries. Around~20% of patients are refractory to high-dose intravenous immunoglobulin (IVIG), the standard treatment, and are at high risk of developing coronary artery aneurysms. Hypothesis: Whole genome sequencing (WGS) will identify specific predictors of non-response and inform the mechanism of IVIG action. Methods: KD patients were diagnosed by the American Heart Association and the American Academy of Pediatrics (AHA/AAP) criteria and treated by AHA guidelines. IVIG refractoriness was defined by persistent or recurrent fever (>38C)>36 hours after completing infusion. We performed a case-control study with WGS on DNA from saliva or blood from 107 responders versus 103 non-responders. After processing informatics using the pipeline of Genome Analysis Toolkit (GATK), additive genetic models were assessed for all common variants using logistic regression. We adjusted for age, gender, and race based on principal components. We also conducted SNP-set (Sequence) Kernel Association Test (SKAT) with common and rare variants in the gene regions with the most statistically significant SNP results. Results: Average sequencing depth was 30x and with a total of 34,548,910 variants. While SNPs in genes previously indicated in the IVIG pathway were confirmed, multiple novel SNPs in various gene regions were also statistically significant (often p< 10-6; Figure-Manhattan plot). SKAT analysis suggested joint effects of multiple SNPs in individual gene regions. Conclusions: We confirmed SNPs in genes from previous reports and identified multiple novel ones, indicating plausible previous unsuspected IVIG mechanisms pathways. Potentially, functional disruption of these genes could lead to non-response. Further, a panel of these SNPs can be a prognostic tool for identifying at-risk KD patients that require therapy intensification.

科研通智能强力驱动
Strongly Powered by AbleSci AI
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
ioi发布了新的文献求助10
刚刚
1秒前
罗远远完成签到,获得积分10
1秒前
LLLL发布了新的文献求助10
1秒前
zy发布了新的文献求助10
2秒前
在水一方的应助被头猫头采纳,获得10
2秒前
大模型的应助被0011采纳,获得10
2秒前
深情安青的应助被幻天游采纳,获得10
2秒前
Reyna发布了新的文献求助10
2秒前
2秒前
2秒前
星辰大海的应助被汪进辉_Will采纳,获得10
2秒前
洁净晓绿完成签到 ,获得积分10
3秒前
orixero的应助被下一回采纳,获得10
3秒前
3秒前
3秒前
LL完成签到,获得积分10
4秒前
4秒前
5秒前
廾匸发布了新的文献求助10
5秒前
传奇3的应助被夬月十三采纳,获得10
5秒前
6秒前
6秒前
TEE的应助被大方树叶采纳,获得10
6秒前
肥子发布了新的文献求助10
6秒前
junjun发布了新的文献求助10
6秒前
6秒前
WU发布了新的文献求助10
7秒前
jiangxia发布了新的文献求助10
7秒前
7秒前
michael发布了新的文献求助10
7秒前
zy完成签到,获得积分10
7秒前
7秒前
Rime完成签到 ,获得积分10
8秒前
8秒前
9秒前
9秒前
zzc完成签到,获得积分10
9秒前
山与海完成签到,获得积分10
9秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Encyclopedia of Modern Artificial Intelligence 1000
Das Matthäusevangelium: Kapitel 1:1–17 1000
IRTSD: Open-Source Data and Toolset for Electromagnetic Transient Analysis of Disturbances and IBR Control Malfunctions in Transmission Systems 1000
Transcriptional Profiling Shows that Gcn4p Is a Master Regulator of Gene Expression during Amino Acid Starvation in Yeast 750
Entre Praga y Madrid : los contactos checoslovaco-españoles (1948-1977) 600
A REVIEW OF THE V-22 DYNAMICS VALIDATION PROGRAM 600
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 计算机科学 工程类 有机化学 化学工程 生物化学 物理 复合材料 内科学 催化作用 光电子学 人工智能 细胞生物学 无机化学 物理化学 数学
热门帖子
关注 科研通微信公众号,转发送积分 8126362
求助须知:如何正确求助?哪些是违规求助? 9529486
关于积分的说明 21579050
捐赠科研通 7706359
什么是DOI,文献DOI怎么找? 3416728
关于科研通互助平台的介绍 2542408
邀请新用户注册赠送积分活动 2457883