Cvijanovich Natalie Z, Anas Nick, Allen Geoffrey L, Thomas Neal J, Bigham Michael T, Weiss Scott L, Fitzgerald Julie, Checchia Paul A, Meyer Keith, Quasney Michael, Gedeit Rainer, Freishtat Robert J, Nowak Jeffrey, Raj Shekhar S, Gertz Shira, Grunwell Jocelyn R, Opoka Amy, Wong Hector R
1Department of Pediatrics, UCSF Benioff Children's Hospital Oakland, Oakland, CA. 2Department of Pediatrics, Children's Hospital of Orange County, Orange, CA. 3Department of Pediatrics, Children's Mercy Hospital, Kansas City, MO. 4Department of Pediatrics, Penn State Hershey Children's Hospital, Hershey, PA. 5Department of Pediatrics, Akron Children's Hospital, Akron, OH. 6Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, PA. 7Department of Pediatrics, Texas Children's Hospital and Baylor College of Medicine, Houston, TX. 8Department of Pediatrics, Miami Children's Hospital, Miami, FL. 9Department of Pediatrics, C.S. Mott Children's Hospital at the University of Michigan, Ann Arbor, MI. 10Department of Pediatrics, Children's Hospital of Wisconsin, Milwaukee, WI. 11Department of Pediatrics, Children's National Health System, Washington, DC. 12Department of Pediatrics, Children's Hospital and Clinics of Minnesota, Minneapolis, MN. 13Department of Pediatrics, Riley Hospital for Children, Indianapolis, IN. 14Department of Pediatrics, Hackensack University Medical Center, Joseph M. Sanzari Children's Hospital, Hackensack, NJ. 15Department of Pediatrics, Children's Healthcare of Atlanta at Egleston, Atlanta, GA. 16Division of Critical Care Medicine, Cincinnati Children's Hospital Medical Center and Cincinnati Children's Research Foundation, Cincinnati, OH. 17Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.
Pediatr Crit Care Med. 2017 Apr;18(4):299-303. doi: 10.1097/PCC.0000000000001058.
Polymorphisms of the glucocorticoid receptor gene are associated with outcome and corticosteroid responsiveness among patients with inflammatory disorders. We conducted a candidate gene association study to test the hypothesis that these polymorphisms are associated with outcome and corticosteroid responsiveness among children with septic shock.
We genotyped 482 children with septic shock for the presence of two glucocorticoid receptor polymorphisms (rs56149945 and rs41423247) associated with increased sensitivity and one glucocorticoid receptor polymorphism (rs6198) associated with decreased sensitivity to corticosteroids. The primary outcome variable was complicated course, defined as 28-day mortality or the persistence of two or more organ failures 7 days after a septic shock diagnosis. We used logistic regression to test for an association between corticosteroid exposure and outcome, within genotype group, and adjusted for illness severity.
Multiple PICUs in the United States.
Standard care.
There were no differences in outcome when comparing the various genotype groups. Among patients homozygous for the wild-type glucocorticoid receptor allele, corticosteroids were independently associated with increased odds of complicated course (odds ratio, 2.30; 95% CI, 1.01-5.21; p = 0.047).
Based on these glucocorticoid receptor polymorphisms, we could not detect a beneficial effect of corticosteroids among any genotype group. Among children homozygous for the wild-type allele, corticosteroids were independently associated with increased odds of poor outcome.
糖皮质激素受体基因多态性与炎症性疾病患者的预后及皮质类固醇反应性相关。我们开展了一项候选基因关联研究,以检验这些多态性与感染性休克患儿的预后及皮质类固醇反应性相关这一假设。
我们对482例感染性休克患儿进行基因分型,检测两个与敏感性增加相关的糖皮质激素受体多态性(rs56149945和rs41423247)以及一个与皮质类固醇敏感性降低相关的糖皮质激素受体多态性(rs6198)。主要结局变量为复杂病程,定义为感染性休克诊断后28天死亡率或7天后持续存在两种或更多器官功能衰竭。我们使用逻辑回归分析在基因型组内检测皮质类固醇暴露与结局之间的关联,并对疾病严重程度进行校正。
美国多个儿科重症监护病房。
标准治疗。
比较不同基因型组时,结局无差异。在野生型糖皮质激素受体等位基因纯合的患者中,皮质类固醇与复杂病程几率增加独立相关(比值比,2.30;95%置信区间,1.01 - 5.21;p = 0.047)。
基于这些糖皮质激素受体多态性,我们在任何基因型组中均未检测到皮质类固醇的有益作用。在野生型等位基因纯合的儿童中,皮质类固醇与不良结局几率增加独立相关。