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Published on: October 13, 2018
Serum insulinlike growth factor-I in biliary atresia
Shigehiko Yoshida1, Masaki Nio, Yutaka Hayashi
1Department of Pediatric Surgery, Tohoku University School of Medicine, Sendai, Japan.
Insights
Children with biliary atresia (BA) show lower Insulin-like Growth Factor-I (IGF-I) levels, particularly those not needing liver transplants. This may indicate more severe liver disease in BA patients.
Area of Science:
- Pediatric Gastroenterology
- Endocrinology
- Hepatology
Background:
- Low Insulin-like Growth Factor-I (IGF-I) levels are noted in children with chronic liver disease, including biliary atresia (BA), awaiting liver transplantation.
- Previous studies have not investigated IGF-I levels in BA patients managed without liver transplantation.
Purpose of the Study:
- To investigate IGF-I levels in children with biliary atresia (BA) who have undergone surgery and are managed without liver transplantation.
- To compare IGF-I levels between BA patients and a control group with normal liver function.
Main Methods:
- IGF-I and growth hormone (GH) were measured in 21 postoperative BA patients and 17 choledochal cyst (CC) patients.
- IGF-I levels were converted to an "IGF%" index to account for age and gender variations.
- IGF% was analyzed in relation to disease severity markers like Kasai's type, jaundice status, esophageal varices, choline esterase, and TTT.
Main Results:
- IGF% was significantly lower in BA patients compared to CC controls.
- Lower IGF% was observed in Kasai's type III BA and in patients with esophageal varices.
- A positive correlation was found between choline esterase and IGF%, and a negative correlation between TTT and IGF%.
Conclusions:
- Low IGF-I levels are characteristic of BA, especially in patients not requiring liver transplantation.
- Reduced IGF-I may reflect the severity of hepatic fibrosis and reduced functioning liver volume in BA.
- IGF% serves as a potential indicator of liver pathology severity in BA.
Background/Purpose:
Low level of Insulinlike growth factor-I (IGF-I) has been reported in children with chronic liver disease like biliary atresia (BA) awaiting liver transplantation. However, there has been no report on IGF-I in BA managed without liver transplantation.
Methods:
The authors measured IGF-I and growth hormone (GH) in 21 postoperative BA, and 17 choledochal cysts (CC) as a control with normal liver function. To avoid an influence of aging, IGF-I was analyzed after converting them into a newly defined index "IGF%." IGF% is proportional to the lower limit of the value of IGF-I in gender- and age-matched normal control previously reported in literature.
Results:
IGF% in BA was significantly lower than that in CC. IGF% tended to be lower in Kasai's type III (atresia at the porta hepatis) and higher in the jaundice-free group. IGF% in patients with esophageal varices was significantly lower. The correlation between choline esterase and IGF% was positive and that for TTT and IGF% was negative.
Conclusions:
Low level of IGF-I is a characteristic finding in BA, especially in patients without need of liver transplantation. And it may reflect the severity of pathologic changes (ie, hepatic fibrosis and reduced volume of normally functioning liver) in BA liver.
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