Bunker-Wiersma Heleen E, Koopmans Richard P, Kuipers Taco W, Knoester Hennie, Bos Albert P
Pediatric Intensive Care Unit, The Emma Children's hospital/Academic Medical Center, Amsterdam, Netherlands.
Pediatr Crit Care Med. 2008 Sep;9(5):517-23. doi: 10.1097/PCC.0b013e318184985b.
In the course of a meningococcal infection, invasive and severe disease occurs in a restricted number of individuals. The predominant mechanism of death in case of meningococcal septic shock is circulatory failure. Inotropic requirements between patients vary widely. We investigated whether polymorphisms in genes regulating the hemodynamic response influence the amount of inotropics required or the susceptibility to severe meningococcal disease.
Retrospective case control study.
Single-center pediatric intensive care unit (PICU).
Fifty-six cases (all consecutive patients admitted to the PICU between 1993 and 2001 with a proven meningococcal infection) and 136 controls. Patients were divided into two groups according to their inotropic requirements.
DNA analysis was performed to determine the polymorphisms of the beta-adrenergic receptor gene-1, beta-adrenergic receptor gene-2, alpha-adducin, angiotensin converting enzyme, and angiotensin II type-1 receptor-1 genes.
For the alpha-adducin gene a significant difference of the genotype distribution was found between the cases and controls. The odds ratio for admission to the PICU with meningococcal sepsis with or without meningitis, for carriers of the variant allele (Gly460Trp or Trp460Trp) was 2.1 (95% confidence interval 1.11-4.04; p < 0.02). Cases, homozygote for the wild-type allele of the beta-1 adrenergic receptor at locus 389, were more likely to have a low pediatric risk of mortality score on admission (odds ratio 3.6, 95% confidence interval 1.11-11.76). No difference was found in the distribution of the beta-adrenergic receptor gene-1, beta-adrenergic receptor gene-2, angiotensin converting enzyme, and angiotensin II type-1 receptor-1 polymorphisms between the two groups of patients or between cases and controls.
Among patients admitted to the PICU with a meningococcal infection, the variant allele of the alpha-adducin gene was more prevalent compared with controls. Patients with the variant allele of the beta-adrenergic receptor gene-1 at locus 389 were more likely to have a high pediatric risk of mortality score on admission. The mechanism and clinical relevance of these findings is unclear.
在脑膜炎球菌感染过程中,侵袭性和严重疾病仅发生在少数个体中。脑膜炎球菌性脓毒症休克患者的主要死亡机制是循环衰竭。患者之间的强心药需求量差异很大。我们研究了调节血流动力学反应的基因多态性是否会影响所需强心药的用量或对严重脑膜炎球菌病的易感性。
回顾性病例对照研究。
单中心儿科重症监护病房(PICU)。
56例病例(1993年至2001年间所有连续入住PICU且确诊为脑膜炎球菌感染的患者)和136名对照。根据患者对强心药的需求将其分为两组。
进行DNA分析以确定β-肾上腺素能受体基因-1、β-肾上腺素能受体基因-2、α-内收蛋白、血管紧张素转换酶和血管紧张素II 1型受体-1基因的多态性。
对于α-内收蛋白基因,病例组和对照组之间的基因型分布存在显著差异。携带变异等位基因(Gly460Trp或Trp460Trp)的患者因脑膜炎球菌败血症伴或不伴脑膜炎入住PICU的比值比为2.1(95%置信区间1.11 - 4.04;p < 0.02)。在第389位点β-1肾上腺素能受体野生型等位基因纯合子的病例,入院时儿童死亡风险评分较低的可能性更大(比值比3.6,95%置信区间1.11 - 11.76)。两组患者之间以及病例组与对照组之间,β-肾上腺素能受体基因-1、β-肾上腺素能受体基因-2、血管紧张素转换酶和血管紧张素II 1型受体-1多态性的分布均未发现差异。
在因脑膜炎球菌感染入住PICU的患者中,与对照组相比,α-内收蛋白基因的变异等位基因更为普遍。第389位点β-肾上腺素能受体基因-1变异等位基因的患者入院时儿童死亡风险评分较高的可能性更大。这些发现的机制和临床相关性尚不清楚。