Sodhi Komal, Bracero Lucas, Feyh Andrew, Nichols Alexandra, Srikanthan Krithika, Latif Tariq, Preston Deborah, Shapiro Joseph I, Elitsur Yoram
Department of Surgery and Pharmacology, Joan C. Edwards School of Medicine, Marshall University, USA.
Department of Internal Medicine, Joan C. Edwards School of Medicine, Marshall University, USA.
J Clin Cell Immunol. 2016 Feb;7(1). doi: 10.4172/2155-9899.1000393. Epub 2016 Feb 17.
Obesity, an epidemic among West Virginia children, as well as insulin resistance (IR), is well-established contributors to nonalcoholic steatohepatitis (NASH). Progression of NASH can lead to hepatic fibrosis and cirrhosis, making early detection imperative. The standard for diagnosing NASH is histologically liver biopsy, which is highly invasive and generally contraindicated in children. By studying serum biomarkers associated with NASH, we aim to identify high risk children who can benefit from a less invasive, alternative approach to the early detection of NASH.
Seventy one children were prospectively recruited and divided into 3 groups: . Serum samples were drawn for each patient and biomarker levels were assessed ELISA kits.
and patients had significantly elevated levels of lipid metabolism and accumulation markers (FGF-21, NEFA, FATP5, ApoB), oxidative stress markers (dysfunctional HDL, 8-Isoprostane), inflammatory markers(dysfunctional HDL, CK-18) and apoptosis markers (CK-18) compared to control patients (p<0.02). Bilirubin (an antioxidant) was significantly decreased in the and patients compared to control (p<0.02).
This study showed a correlation between obesity, IR, and biomarkers associated with NASH in pediatrics patients from West Virginia, with obese with IR patients showing the strongest correlation. These findings support the clinical application of these serum biomarkers as a less invasive method for early detection of NASH and hepatic fibrosis.