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Protocol for the Assessment of Variability in Histology and Gene Expression in Bariatric Surgery Patients.

16 december 2011 uppdaterad av: Mary Rinella, Northwestern University
It is known that a vast majority of patients seeking a bariatric surgery weight reduction procedure have non-alcoholic fatty liver disease (NAFLD), while a smaller subset of patients within this group have a more serious liver problem known as nonalcoholic steatohepatitis (NASH). NASH is a serious liver disease that can lead to cirrhosis, liver failure and ultimately liver transplantation. The purpose of this study is to explore the effects of bariatric surgery on the progression of NASH. The investigators also hope to gain insight into which genes may be responsible for the development of NAFLD and NASH. The knowledge gained from this study will advance the field of fatty liver disease and help design rational treatments to prevent disease progression.

Studieöversikt

Status

Avslutad

Betingelser

Detaljerad beskrivning

Nonalcoholic fatty liver disease (NAFLD) is the most common cause of abnormal liver tests in the United States. NAFLD is often found in association with obesity and diabetes and it is expected to become increasingly prevalent as the incidence of diabetes and obesity continues to increase. NAFLD represents a range of diseases from simple fatty deposition in the liver to more aggressive inflammation and fibrosis, termed nonalcoholic steatohepatitis (NASH). The distinction of NASH as an entity within NAFLD is an important one, as the natural history of this disease is different. Ultimately, NASH may progress to cirrhosis in up to 25% of patients, compared to simple steatosis which is a benign condition.

NAFLD has been estimated at 10-24% in various populations and is significantly higher in obese populations (57.5-74%). NASH is a subset of NAFLD characterized by fatty change with lobular inflammation, hepatocellular injury, progressive fibrosis and cirrhosis. The bariatric surgery population is an ideal cohort to study a large subset of NASH; those with morbid obesity.

The purpose of this study is to examine variability of hepatic histology as well as expression of key metabolic genes in NAFLD/NASH patients undergoing bariatric surgery. Patients will undergo pre-operative laboratory testing, followed by intra-operative liver and fat biopsies. A 12-month follow up will consist of repeat liver biopsy and laboratory testing. We predict that histologic variability of inflammation and fibrosis in NASH is accompanied by differential gene expression. Furthermore, if this variability is pronounced, this will temper the reliance on percutaneous liver biopsy in NASH as the "gold standard" and further emphasize the need for global markers of disease progression.

Studietyp

Observationell

Inskrivning (Faktisk)

43

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

    • Illinois
      • Chicago, Illinois, Förenta staterna, 60611
        • Northwestern University

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år till 65 år (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Testmetod

Icke-sannolikhetsprov

Studera befolkning

This will be a prospective trial of obese patients with presumed NAFLD undergoing bariatric surgery. Patients will be enrolled at Northwestern Memorial Hospital through the bariatric surgery clinic.

Beskrivning

Inclusion Criteria:

  • Subjects must be willing to give written informed consent
  • Subjects must fulfill the criteria for bariatric surgery that have been recommended by a National Institutes of Health (NIH) consensus conference.

These criteria include:

  1. The patient should be greater than 100 pounds above desirable body weight or a Body Mass Index (BMI) >40 kg/m2.
  2. Presence of significant obesity-related illnesses with a BMI of 35-40 kg/m2.
  3. Failure of sustained weight loss on supervised dietary and/or medical regimens.
  4. Patient shows understanding of the risks and benefits of surgery and understands lifestyle changes subsequent to the operation.
  5. Acceptable operative risk.

    • Adult subjects 18-65 years of age of any race or gender

Exclusion Criteria:

  • Anti - smooth muscle Ab < 1:80.
  • Serum Hepatitis B surface antigen (HepBsAg) negative.
  • Serum Hepatitis C Antibody (HepC Ab) negative
  • Iron/TIBC ratio (transferrin saturation) < 45%
  • Alpha-1-antitrypsin level within normal limits
  • Ceruloplasmin level within normal limits.
  • Negative pregnancy test (females)
  • No active drug abuse or within 6 months
  • Etoh consumption < 20g/day (males) or < 10 g/day (females) - Assessed by one physician and confirmed with one family member.
  • No known diagnosis of malignancy
  • Any other conditions which the investigator feels would make the subject unsuitable for enrollment, or could interfere with the subject completing the protocol.

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Observationsmodeller: Case-Control
  • Tidsperspektiv: Blivande

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Utredare

  • Huvudutredare: Mary E. Rinella, MD, Northwestern University

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart

1 september 2006

Avslutad studie (Faktisk)

1 september 2008

Studieregistreringsdatum

Först inskickad

19 januari 2006

Först inskickad som uppfyllde QC-kriterierna

19 januari 2006

Första postat (Uppskatta)

23 januari 2006

Uppdateringar av studier

Senaste uppdatering publicerad (Uppskatta)

20 december 2011

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

16 december 2011

Senast verifierad

1 december 2011

Mer information

Termer relaterade till denna studie

Ytterligare relevanta MeSH-villkor

Andra studie-ID-nummer

  • 1347-004

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

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