Calcitonin gene-related peptide and its correlation with prognosis in severe pneumonia among children below 6 years at PICU of Al Zahraa university hospital.

Sara Saad, Soheir Ibrahim, Shimaa Moustafa, Fatma Elzhraa Ae Diab
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Abstract

Pneumonia is known to be the biggest cause of death in children younger than five years old. In pulmonary diseases such as pulmonary arterial hypertension, asthma, acute lung injury, and pulmonary fibrosis, calcitonin gene related peptide (CGRP) has been linked to the regulation of inflammation, proliferation, and fibrosis. However, its ability to foretell the emergence of severe pneumonia is questionable. We aimed to determine whether blood levels of CGRP correlate with the outcome of critically ill children. This case-control study included 45 children with severe pneumonia admitted to the pediatric intensive care unit and 45 children with matched age and sex as controls. We investigated the serum level of CGRP as well as routine laboratory investigations of both groups. The CGRP level was lower in the patient group with median of 77 ng/L ranged from 55 to 183 as compared to control group with median of 230 ng/L ranged from 133 to 664 (p≤0.001). Also, CGRP level was significantly higher in the survived group with median of 96.1 ng/L ranged from 55 to 183 than the non-survived group with median of 63.4 ng/L ranged from 55.5 to 120.9 (p=0.022). In conclusion, we found that serum level of CGRP was extremely low in critical and extremely critically ill patients, and thus can be used as a predictor of mortality in children with severe pneumonia.

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Al Zahraa大学医院PICU 6岁以下儿童重症肺炎患者降钙素基因相关肽及其与预后的相关性。
众所周知,肺炎是五岁以下儿童死亡的最大原因。在肺动脉高压、哮喘、急性肺损伤和肺纤维化等肺部疾病中,降钙素基因相关肽(CGRP)与炎症、增殖和纤维化的调节有关。然而,它预测严重肺炎出现的能力值得怀疑。我们的目的是确定CGRP的血液水平是否与危重儿童的预后相关。这项病例对照研究包括45名入住儿科重症监护室的重症肺炎儿童和45名年龄和性别匹配的儿童作为对照。我们调查了两组患者的血清CGRP水平以及常规实验室调查。患者组CGRP水平较低,中位数为77 ng/L,范围为55-183,而对照组的CGRP水平中位数为230 ng/L,从133到664(p≤0.001)。此外,存活组的CGRP水平显著高于未存活组,中位数为96.1 ng/L,在55-183,范围为55.5到120.9(p=0.022)。总之,我们发现,危重和极危重患者的血清CGRP水平极低,因此可以作为重症肺炎儿童死亡率的预测指标。
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CiteScore
1.20
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52
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