Family Studies in Primary Biliary Cirrhosis (PBC)

03:33 EDT 17th September 2014 | BioPortfolio

Summary

Primary biliary cirrhosis (PBC) is a chronic liver disease primarily affecting middle age women. It is characterized by immune-mediated damage to cells lining the tiny bile ducts within the liver. Although the underlying cause of PBC is likely to be multifactorial, the epidemiologic/population data indicate a very important role for genetic predisposition, meaning that the disease seems to run in families. Susceptibility genes for PBC have not been identified possibly due to limitations such as small sample size in prior studies. The primary objective of this study is to identify these genes. This study involves obtaining clinical and demographic data as well as collecting DNA samples from patients and their parents, and siblings to screen for a select set of candidate genes as well as the full genome for variants associated with PBC.

Description

This proposal is predicated on cumulative data revealing a major role for genetic factors in PBC and the recent positional cloning of genes for Crohn’s disease, type 2 diabetes and rheumatoid as well as psoriatic arthritis data provide the “proof-of-principle” that susceptibility genes for multigenic diseases can be identified by linkage and association strategies. Our group has access to >600 patients with PBC and these individuals plus family members provide an excellent resource for PBC gene discovery. Moreover, an International PBC Consortium we have initiated will serve not only to validate our findings but also to serve as a source for additional patient accrual should we be searching for genes with very small effects. Thanks to the remarkable advances in genotyping technology and sequence data emanating from the Human Genome Project, patient populations such as ours can now be fully mined so as to identify susceptibility genes for common multigenic diseases. By combining the patient resources of our group and that of other Canadian centers with available knowledge of the full genome sequence and the extensive information on SNPs within this sequence, as well as our expertise in high throughput genotyping and rapid computational approaches of genetic data, we are very well positioned to begin delineating the susceptibility alleles for PBC. As such alleles are identified, the information will then be used to define the molecular pathophysiology of this disease, to determine whether genetic markers can be used to predict risk and/or stratify patients in relation to prognosis and drug responsiveness, and ultimately, to identify novel targets for improved therapeutic intervention.

For the purposes of this study only patients with a definite diagnosis of PBC will be recruited ie:- those that had an elevated serum alkaline phosphatase level and positive AMA by ELISA or immunofluorescence (>1/40 titer) at the time of their initial diagnosis and who have had a liver biopsy which confirmed the diagnosis of PBC. After signing the consent form the patients will complete a questionnaire. With the patient’s permission the coordinator will contact the patient’s parents and siblings that are either affected or unaffected by PBC to ask them to participate in the study. A total of five tubes of blood will be taken from each participant in the study. The blood samples will be used to study the liver biochemistries and to study the inherited genetic material (DNA) in order to find out what causes PBC. In addition we are going to review the medical records for all the patients with PBC from TWH recruited to this study using the records held in Misys to examine and verify their medical and surgical history, past physical exams, laboratory tests and treatments. Each patient will also be asked to recruit unrelated (usually spouses) household members or friends who live locally to act as controls. They will then be treated similarly with regard to the consent form, questionnaire and blood work.

The plan is to have approximately 600 patients with PBC along with approximately 1800 of their relatives and other unrelated healthy volunteers to take part in this study – this is a multicentre study – sites being Toronto, London and Halifax.

Statistical Analyses/Power Calculations: The use of association analysis to identify susceptibility alleles is highly dependent on linkage disequilibrium (LD) between the SNP markers and the disease loci. To demonstrate the extent to which LD can be used to delineate PBC loci, our collaborator Dr. C. Amos has carried out calculations of the power to detect significant effects (at the p ≤ 0.05 level) in a case-control analysis assuming different amount of LD. Dr. Amos directs a statistical genetics group at MD Anderson Cancer Centre and is a longstanding collaborator of K. Siminovitch. He and his group members are also the statistical advisors to several disease-mapping consortia, such as NARAC, a US-based consortium for discovery of rheumatoid arthritis genes. To estimate the power of an association study to identify PBC susceptibility alleles, Dr. Amos used data from Talwalkar and Lindor, estimating PBC prevalence at 0.05% among adult females and a 15 fold increased risk for PBC among first-degree relatives of affected individuals. Assuming that mutation frequency for disease causation is 0.1% and also that PBC is caused by a single gene, then this level of risk among affected first-degree relatives implies the penetrance among carriers of PBC susceptibility alleles to be 6% and among non-carriers to be 0.4%. A single gene model for PBC, however, is simplistic and not consistent with available epidemiologic data. If instead, an assumption of 4 disease causative loci is made and risk is thus assigned to each one of these loci, then the genotype-specific risk would be 2.6%, the locus-specific relative risk would be a more modest 3.75, and the disease allelic frequency in carriers would be 10%. In the studies proposed here, we will begin by studying 300 cases and 300 controls for PBC association with specific candidate genes discussed above. The power to detect association in any case-control study is highly dependent upon the LD between the disease mutation and the SNPs at closely linked loci as well as the number of genes studied (about 40). If we assume a high level of disequilibrium, the disequilibrium coefficient (D’) being 0.9 and, to be conservative, apply Bonferroni’s correction for the simultaneous evaluation of 40 loci, then achieving 5% power in this study will require obtaining a single SNP test p-value of 0.00125. Based on a disease allele frequency of 10% (as calculated above), and the analysis of 300 cases and 300 controls, the power to detect a SNP marker-disease association would then be 84%. The study can be further powered by increasing numbers of cases and/or controls. Thus, to conserve resources, genotyping will be initially carried out using 300 cases and 300 controls, but an additional 300 controls will be further genotyped for any markers showing significant results at the p=0.01 level. Genome-wide association analyses will also be carried out initially on the 300 cases and controls. However, because a genome-wide screen is likely to yield many false positive loci-disease associations, any loci showing association at the 5% level will be confirmed using a replicate set of 300 cases and controls and/or trio families, once 200 such families are available.

Study Design

Observational Model: Defined Population, Time Perspective: Cross-Sectional, Time Perspective: Prospective

Conditions

Biliary Cirrhosis, Primary

Location

Liver Clinic, Toronto Western Hospital, UHN
Toronto
Ontario
Canada
M5T 2S8

Status

Recruiting

Source

University Health Network, Toronto

Results (where available)

View Results

Links

Clinical Trials [213 Associated Clinical Trials listed on BioPortfolio]

Study of Combivir for Patients With Primary Biliary Cirrhosis

This is a proof of principal study to determine whether combination anti-viral therapy with Combivir impacts on hepatic biochemistry in patients with primary biliary cirrhosis

Use of Fenofibrate for Primary Biliary Cirrhosis

This is a pilot study to evaluate the safety and efficacy of fenofibrate on patients with primary biliary cirrhosis who have an incomplete response to ursodeoxycholic acid.

Moexipril for Primary Biliary Cirrhosis

The blockade of angiotensin II synthesis attenuates hepatic fibrosis in different experimental models of chronic liver injury. We aimed to determine the safety and efficacy of moexipril, a...

Initial Study of Rituximab to Treat Primary Biliary Cirrhosis

The purpose of this study is to determine the safety of the anti-CD20 antibody rituximab in treating patients with Primary Biliary Cirrhosis (PBC). Rituximab is a laboratory-made antibody ...

Oral Budesonide in the Treatment of Patients With Primary Biliary Cirrhosis and Overlap Features of Autoimmune Hepatitis

The purpose of the study is to find out the effects Budesonide, 9 mg daily for one year, has on patients with Primary Biliary Cirrhosis with features of autoimmune hepatitis.

PubMed Articles [7395 Associated PubMed Articles listed on BioPortfolio]

High Frequency of Antiphospholipid Antibodies in Primary Biliary Cirrhosis.

To evaluate, retrospectively, the frequency of autoantibodies of antiphospholipid syndrome (APLS) in Tunisian patients with primary biliary cirrhosis (PBC).

Telomere dysfunction in peripheral blood mononuclear cells from patients with primary biliary cirrhosis.

Chromosomal instability in peripheral blood mononuclear cells has a role in the onset of primary biliary cirrhosis. We hypothesized that patients with primary biliary cirrhosis may harbour telomere dy...

Clinicopathological study of primary biliary cirrhosis with interface hepatitis compared to autoimmune hepatitis.

To investigate histological and immunohistochemical differences in hepatitis between autoimmune hepatitis (AIH) and primary biliary cirrhosis (PBC) with AIH features.

Infiltration of inflammatory cells expressing mitochondrial proteins around bile ducts and in biliary epithelial layer may be involved in the pathogenesis in primary biliary cirrhosis.

Serum antimitochondrial antibodies are characteristic in most patients with primary biliary cirrhosis (PBC); however, the significance of antimitochondrial antibodies in the pathogenesis of PBC remain...

Meta-Analysis Assessment of GP210 and SP100 for the Diagnosis of Primary Biliary Cirrhosis.

To conduct a systematic review of included studies assessing the association of GP210 and SP100 with the risk of primary biliary cirrhosis (PBC) using meta-analysis.

Medical and Biotech [MESH] Definitions

FIBROSIS of the hepatic parenchyma due to obstruction of BILE flow (CHOLESTASIS) in the intrahepatic or extrahepatic bile ducts (BILE DUCTS, INTRAHEPATIC; BILE DUCTS, EXTRAHEPATIC). Primary biliary cirrhosis involves the destruction of small intra-hepatic bile ducts and bile secretion. Secondary biliary cirrhosis is produced by prolonged obstruction of large intrahepatic or extrahepatic bile ducts from a variety of causes.

Chronic inflammatory disease of the BILIARY TRACT. It is characterized by fibrosis and hardening of the intrahepatic and extrahepatic biliary ductal systems leading to bile duct strictures, CHOLESTASIS, and eventual BILIARY CIRRHOSIS.

Infection of the biliary passages with CLONORCHIS SINENSIS, also called Opisthorchis sinensis. It may lead to inflammation of the biliary tract, proliferation of biliary epithelium, progressive portal fibrosis, and sometimes bile duct carcinoma. Extension to the liver may lead to fatty changes and cirrhosis. (From Dorland, 27th ed)

Abnormal passage in any organ of the biliary tract or between biliary organs and other organs.

A tool for the study of liver damage which causes bile stasis and hyperbilirubinemia acutely and bile duct hyperplasia and biliary cirrhosis chronically, with changes in hepatocyte function. It may cause skin and kidney damage.

More From BioPortfolio on "Family Studies in Primary Biliary Cirrhosis (PBC)"

Search BioPortfolio:
Loading
Advertisement

Relevant Topics

Women's Health
Latest News Clinical Trials Research Drugs Reports Corporate
Women's Health - key topics include breast cancer, pregnancy, menopause, stroke Follow and track Women's Health News on BioPortfolio: Women's Health News RSS Women'...

Bioinformatics
Latest News Clinical Trials Research Drugs Reports Corporate
Bioinformatics is the application of computer software and hardware to the management of biological data to create useful information. Computers are used to gather, store, analyze and integrate biological and genetic information which can then be applied...

Advertisement