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Complement factor 3 among children with hepatitis A: Assessment of bilirubin levels
Wei Lin1, Jing Zhang1, Jian Zhang1
1Beijing Youan Hospital, Capital Medical University.
Insights
Complement factor 3 (C3) levels are decreased in children with hepatitis A, particularly those with hyperbilirubinemia. Lower C3 indicates a more severe disease course in pediatric hepatitis A patients.
Area of Science:
- Pediatric Infectious Diseases
- Immunology
- Hepatology
Background:
- Hepatitis A is a viral infection affecting the liver.
- Complement factor 3 (C3) plays a role in immune response.
- Understanding C3 levels in pediatric hepatitis A can offer insights into disease severity.
Purpose of the Study:
- To evaluate complement factor 3 (C3) levels in children diagnosed with hepatitis A.
- To compare C3 levels between patients with varying degrees of hyperbilirubinemia and healthy controls.
Main Methods:
- An observational study involving 100 children with hepatitis A and age/gender-matched healthy controls.
- Patients were categorized into two groups based on total bilirubin levels (≤2mg/dl and >2mg/dl).
- Serum C3 levels were measured and analyzed using SPSS 13.
Main Results:
- Children with hepatitis A had significantly lower C3 levels compared to controls.
- Patients with higher bilirubin levels (Group B) exhibited lower C3 levels than those with lower bilirubin (Group A).
- C3 levels negatively correlated with total bilirubin and alanine aminotransferase, and positively with prothrombin time activity.
Conclusions:
- Complement factor 3 (C3) levels are reduced in children hospitalized with hepatitis A.
- Decreased C3 levels are particularly pronounced in pediatric hepatitis A cases with hyperbilirubinemia.
- C3 may serve as a potential indicator of disease severity in pediatric hepatitis A.
Objective:
To evaluate the complement factor 3 levels in children with hepatitis A.
Methods:
This observational study was conducted at the Infectious Diseases Hospital of Hotan District, China, from September 2014 to January 2015, and comprised children with hepatitis A and controls. The patients were divided into two groups. The ones with total bilirubin less than or equal to 2mg/dl comprised group A, while the ones whose total bilirubin was more than 2mg/dl was named group B. Besides, we enrolled age- and gender-matched healthy children as controls. SPSS 13 was used for data analysis.
Results:
Of the 100 participants, 41(41%) were in group A, 29(29%) in group B and 30(30%) were controls. The serum level of alanine aminotransferase, aspartate aminotransferase, total bile acid, the incidence of ascites and the incidence of hepatic encephalopathy were significantly increased in patients of group B when compared to group A (p=0.046, p=0.009, p<0.0001, p=0.018 and p=0.026). The levels of prothrombin time activity, total protein and albumin were higher in group A (p<0.0001, p<0.0001, and p <0.0001). Total hepatitis A patients had significantly lower serum complement factor 3 levels compared to normal controls (p =0.018). Group B had significantly lower serum complement factor 3 levels compared to normal controls (p <0.0001) and group A (p<0.0001). In total patients, complement factor 3 levels were negatively correlated with total bilirubin and alanine aminotransferase (p=0.029), while complement factor 3 levels were positively correlated with prothrombin time activity (p=0.001).
Conclusions:
Complement factor 3 values were found to be decreased in children hospitalised with hyperbilirubinaemia hepatitis A.
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