Genetic variants in acute, acute recurrent and chronic pancreatitis affect the progression of disease in children

被引:33
作者
Abu-El-Haija, Maisam [1 ,2 ]
Valencia, C. Alexander [3 ,8 ]
Hornung, Lindsey [4 ]
Youssef, Nour [5 ]
Thompson, Tyler [1 ]
Barasa, Nathaniel W. [6 ,7 ]
Wang, Xinjian [6 ,7 ]
Denson, Lee A. [1 ,2 ]
机构
[1] Cincinnati Childrens Hosp Med Ctr, Gastroenterol Hepatol & Nutr, 3333 Burnet Ave, Cincinnati, OH 45229 USA
[2] Univ Cincinnati, Dept Pediat, Coll Med, Cincinnati, OH USA
[3] Cincinnati Childrens Hosp Med Ctr, Cincinnati, OH 45229 USA
[4] Cincinnati Childrens Hosp Med Ctr, Biostat & Epidemiol, 3333 Burnet Ave, Cincinnati, OH 45229 USA
[5] LAU, Sch Med, Cincinnati Childrens Hosp, Clin Rotat, Lebanon, NH USA
[6] Cincinnati Childrens Hosp Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA
[7] Lab Genet & Genom, 3333 Burnet Ave, Cincinnati, OH 45229 USA
[8] PerkinELmer Genom, 250 Ind Dr, Pittsburgh, PA 15275 USA
关键词
Pediatric pancreatitis; Extensive genetic testing; RISK-FACTORS; MUTATIONS; PRSS1; STANDARDS; ETIOLOGY; SPINK1;
D O I
10.1016/j.pan.2019.05.001
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/objectives: Acute pancreatitis (AP) is emerging in pediatrics. A subset of children with AP progresses to acute recurrent pancreatitis (ARP) and chronic pancreatitis (CP). The role of extensive gene testing in the progression has not been investigated previously. We have followed children enrolled in the registry and at our center for progression to ARP and CP after the first attack. Methods: This study utilizes an extensive gene sequencing panel as a platform to evaluate the role of genetics in first attack AP, and the progression over time, from first attack to ARP and CP in children. Results: Genes, with corresponding variants were involved in the 3 groups studied: AP, ARP and CP. We have shown that the presence of gene variants from the eight tested genes is enriched in the CP group compared to the AP and ARP groups. The presence of more than one gene was associated with CP (p = 0.01). SPINKI mutation(s) was significantly associated with faster progression to ARP, (p = 0.04). Having a variant from CFTR, SPINKI or PRSS1, was associated with the faster progression from AP to CP over time (p <0.05). Conclusions: This study shows that genetics have a significant role in progression to ARP and CP from the first attack of pancreatitis. (C) 2019 IAP and EPC. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:535 / 540
页数:6
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