Abstract | BACKGROUND: METHODS: Concentrations of serum MCP-1 and collagen type IV were measured in 38 patients with BA by using commercially available kits. MCP-1 was also assessed in liver biopsy specimens by using immunohistochemistry. Subjects were classified into groups. Group 1 comprised BA patients with normal liver function (n = 13), group II comprised BA patients with moderate liver dysfunction (n = 18), group III comprised BA patients older than 20 years awaiting liver transplantation (n = 7), and the control group comprised age-matched patients without evidence of liver disease (n = 23). RESULTS: Serum MCP-1 levels were significantly increased in group II compared with group I (P < .0001) and the control group (P < .0001). Serum MCP-1 levels in group III were lower than in the control group (P < .0001). There was a significant linear correlation between serum MCP-1 levels and type IV collagen levels in group II. Group II subjects with portal hypertension (PH) had higher MCP-1 levels than those without PH (P = .0009). Biopsy specimens showed MCP-1 was expressed mainly on biliary epithelial cells, vascular endothelial cells, and hepatocytes in group II. CONCLUSIONS: These findings suggest that MCP-1 probably plays a significant role in the development of progressive liver fibrosis in BA.
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Authors | Hiroyuki Kobayashi, Takuya Tamatani, Tsuyoshi Tamura, Junichi Kusafuka, Hiroyuki Koga, Atsuyuki Yamataka, Geoffrey J Lane, Katsumi Miyahara, Noriyoshi Sueyoshi, Takeshi Miyano |
Journal | Journal of pediatric surgery
(J Pediatr Surg)
Vol. 41
Issue 12
Pg. 1967-72
(Dec 2006)
ISSN: 1531-5037 [Electronic] United States |
PMID | 17161183
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Chemokine CCL2
- Collagen Type IV
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Topics |
- Adolescent
- Biliary Atresia
(blood, complications, physiopathology)
- Chemokine CCL2
(blood)
- Child
- Child, Preschool
- Collagen Type IV
(blood)
- Digestive System Surgical Procedures
- Disease Progression
- Humans
- Hypertension, Portal
(etiology, physiopathology)
- Liver Cirrhosis
(etiology, physiopathology)
- Treatment Outcome
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