Ninety patients with nonalcoholic steatohepatitis: insulin resistance, familial tendency, and severity of disease

IR Willner, B Waters, RS Patil, A Reuben… - Official journal of the …, 2001 - journals.lww.com
IR Willner, B Waters, RS Patil, A Reuben, J Morelli, CA Riely
Official journal of the American College of Gastroenterology| ACG, 2001journals.lww.com
OBJECTIVE: Nonalcoholic steatohepatitis (NASH) is a common but poorly understood liver
disease. Our aim was to study a large group of patients referred for Hepatology consultation
to further characterize this disorder, in particular its demographics and range of severity. We
also sought to better understand its etiology and its relationship to the insulin resistance
syndrome, known as the metabolic syndrome or syndrome X. METHODS: Retrospective
review of 90 patients seen over a 4-yr period. RESULTS: Ninety patients aged 14–70 with …
Abstract
OBJECTIVE:
Nonalcoholic steatohepatitis (NASH) is a common but poorly understood liver disease. Our aim was to study a large group of patients referred for Hepatology consultation to further characterize this disorder, in particular its demographics and range of severity. We also sought to better understand its etiology and its relationship to the insulin resistance syndrome, known as the metabolic syndrome or syndrome X.
METHODS:
Retrospective review of 90 patients seen over a 4-yr period.
RESULTS:
Ninety patients aged 14–70 with NASH seen at the Liver Clinics at either the University of Tennessee or the Medical University of South Carolina. Eleven had complications of portal hypertension and seven of these had undergone or were awaiting transplantation. NASH was seen in nine families either in siblings or in subsequent generations. Diabetes or insulin resistance were present in almost all in this cohort of patients with NASH. Diabetes, hyperlipidemia, hypertension, and atherosclerotic disease, the components of syndrome X, were common in this population.
CONCLUSION:
NASH affects males and females equally, and presents over a wide age range. Despite its usually benign course, 28% of patients had cirrhosis and almost half of those had complications of portal hypertension, necessitating liver transplantation. Obesity was common in affected patients and cirrhosis was more common in the morbidly obese. Familial clustering was common, with 18% of patients having a similarly affected first degree relative. The clinical features that define syndrome X (diabetes, hypertension, hyperlipidemia, and atherosclerotic disease) are common in affected patients. Studies of glucose tolerance demonstrated unsuspected diabetes in six, and insulin resistance (the hallmark of syndrome X) in 85% of those tested. We hypothesize that NASH is a disorder of genetic etiology and is the hepatic manifestation of syndrome X, the insulin resistance syndrome.
Lippincott Williams & Wilkins