NASH CLINICAL RESEARCH NETWORK LAUNCHES TRIAL FOR TREATMENT OF LI VER DISEASE IN CHILDREN

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U.S. Department of Health and Human Services 
NATIONAL INSTITUTES OF HEALTH 
NIH News 
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)  
http://www.niddk.nih.gov/

FOR IMMEDIATE RELEASE: Tuesday, September 27, 2005 

CONTACT: Marcia Vital, 301-496-3583, mv60k@xxxxxxx 

NASH CLINICAL RESEARCH NETWORK LAUNCHES TRIAL FOR TREATMENT OF LIVER DISEASE
IN CHILDREN 

The Nonalcoholic Steatohepatitis (NASH) Clinical Research Network has
launched its second clinical trial to study NASH, a liver disease that
resembles alcoholic liver disease but occurs in patients who drink little or
no alcohol. The first trial, launched in January of this year, focuses on
adults, while the second trial studies the disease in children. The NASH
Clinical Research Network and its clinical trials are funded by the National
Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), one of the
National Institutes of Health (NIH). 

The "Treatment of Nonalcoholic Fatty Liver Disease (NAFLD) in Children"
(TONIC) trial will enroll 180 boys and girls, ages 8-15 years with NAFLD.
The participants will receive vitamin E, or metformin (an
insulin-sensitizing drug), or placebo over 2 years. There are no weight
cut-offs or percentiles for the children participating in TONIC. However,
more than ninety percent of the children are expected to be obese.
Volunteers need a baseline biopsy that demonstrates NAFLD to be eligible for
the study. Children with diabetes and other chronic liver diseases will be
excluded from TONIC. 

While similar to alcoholic liver disease, NAFLD, occurs in persons who drink
little to no alcohol. NAFLD is associated with overweight and obesity and
occurs in a high proportion of persons with diabetes. But, it can also occur
in adults and children who are normal weight without diabetes. Although
there seems to be an association between obesity and liver injury, current
research does not support a causal link or trigger from obesity to liver
injury. TONIC investigators hope to uncover the underlying conditions that
contribute to the development and progression of NAFLD in children. 

Once considered a disease of adults over 40, NAFLD is increasingly reported
in children. Determining population-based prevalence numbers for NAFLD is
difficult. These numbers depend on the age group being studied, the
racial/ethnic mix of the study, and the methods used to assess fatty liver,
which include serum enzyme readings, ultrasound, and magnetic resonance
imaging (MRI). However, researchers in a nationwide school-based population
study found that about 23 percent of obese 17-year-olds had abnormal serum
enzyme levels, an indicator of NAFLD. The major feature in NAFLD is the
accumulation of fat in the liver. Patients with inflammation and liver
injury along with fat in the liver are said to have NASH. Most patients with
fatty liver disease feel well and do not experience symptoms. 

NAFLD can be a precursor to NASH, which may progress to cirrhosis. When
complications such as cirrhosis cannot be controlled with treatment or when
the liver becomes so damaged from scarring that it completely stops
functioning, a liver transplant is necessary. Researchers are concerned that
the disease may progress in children and increase their risk for cirrhosis,
liver failure, and death as adults, particularly if they drink alcohol or
contract viral hepatitis. 

A liver biopsy is the only way to accurately distinguish NASH from simple
fatty liver disease. Most of the children with the disease are overweight
and insulin-resistant, with boys more commonly affected than girls.
Mexican-American children appear to have a greater risk for NASH than black
and white children. 

"The rise in the rates of NAFLD in children likely mirrors the increase in
obesity, making it the most prevalent liver disease in American children
today," says Joel E. Lavine, M.D., Ph.D., chair, NASH-CRN Pediatric
Sub-committee and principal investigator for the center at the University of
California, San Diego. 

Currently, there are no safe or effective drugs recommended to treat
children or adults with this liver disease. Results from small pilot studies
using metformin or antioxidants for children with NAFLD appear to improve
liver enzyme levels and may delay or possibly prevent the progression of
NASH. The children participating in the TONIC trial will receive metformin
as a treatment option because extensive safety and efficacy data exists on
the use of this drug for the treatment of type 2 diabetes in children. 

"As the first randomized, controlled trial for children with NAFLD, TONIC
provides researchers and NIDDK a platform to conduct rigorous studies on how
safe and effective vitamin E and metformin are in treating children with
this liver disease," says Patricia Robuck, Ph.D., M.P.H., project scientist
for the NASH Clinical Research Network and director of the Clinical Trials
Program within the Division of Digestive Diseases and Nutrition at the
NIDDK. 

The adult trial, "Pioglitazone versus Vitamin E versus Placebo for the
Treatment of Nondiabetic Patients with Nonalcoholic Steatohepatitis"
(PIVENS), was initiated earlier this year and will recruit 240 adults with
NASH into three treatment groups: vitamin E group, pioglitazone (an
insulin-sensitizing drug) group, or placebo group. Volunteers will undergo
liver biopsies at the start and the end of the trial. Patient enrollment is
ongoing. 

"The NASH Clinical Research Network and its two randomized controlled trials
offer opportunities to learn more about the cause and natural history of
this liver disease, which will advance treatments and improve patient
outcomes," says Jay Hoofnagle, M.D., director, NIDDK Liver Disease Research
Branch. 

The NASH Clinical Research Network, consisting of eight clinical centers and
a data coordinating center, was formed in September 2002 to conduct research
on the natural history, pathogenesis, and treatment of NASH. With the
information gathered from the observational studies and clinical trials
involving both adults and children with NASH/NAFLD, the Clinical Research
Network will create a database of information to be used by researchers in
the development of treatments for this liver disease. 

The eight clinical centers of the NASH Clinical Research Network recruiting
patients for both the TONIC and PIVENS trials include: Case Western Reserve
University in Cleveland; Duke University Medical Center in Raleigh-Durham
(adult site)/ Johns Hopkins University in Baltimore (pediatric site);
Indiana University in Indianapolis; St. Louis University in Missouri;
University of California in San Diego; University of California in San
Francisco; University of Washington in Seattle; and Virginia Commonwealth
University in Richmond. The Johns Hopkins University Bloomberg School of
Public Health in Baltimore provides coordination of the research network
studies. 

Editors:
-- Contact information for the centers is available at
http://www.nashcrn.com.

-- For general information about NASH, visit
http://digestive.niddk.nih.gov/ddiseases/pubs/nash/. 

The NASH Clinical Research Network, the TONIC trial, and the PIVENS trial
are funded by the National Institute of Diabetes and Digestive and Kidney
Diseases (NIDDK), part of the National Institutes of Health (NIH). The
National Institute of Child Health and Human Development, part of the NIH,
an agency of the U.S. Department of Health and Human Services, provides
additional funding.

The National Institutes of Health (NIH) -- "The Nation's Medical Research
Agency" -- includes 27 Institutes and Centers and is a component of the U.
S. Department of Health and Human Services. It is the primary Federal agency
for conducting and supporting basic, clinical, and translational medical
research, and it investigates the causes, treatments, and cures for both
common and rare diseases. For more information about NIH and its programs,
visit http://www.nih.gov.
  
##
 
This NIH News Release is available online at:
http://www.nih.gov/news/pr/sep2005/niddk-27.htm.

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