Table.
Main characteristics of the studies included in this meta-analysis
Study | Zein et al14 | Corpechot et al12 | Mantaka et al13 |
---|---|---|---|
Country | USA | France | Greece |
Study design | Cross-sectional | Cross-sectional | Cross-sectional |
Year | 2006 | 2010 | 2018 |
Total participants | First cohort: 77 patients with PBC | 164 patients with PBC | 148 patients with PBC |
Second cohort: 155 patients with PBC | |||
Participants | First cohort: Patients with PBC who were seen at one of the three teaching hospitals of Case Western Reserve University (University Hospital, Veteran Affair Medical left and MetroHealth Medical Center) in Cleveland, Ohio, from 1 January 1998 to 31 October 2005 were identified from the databases of the hospitals. Only patients who had liver histopathology available in the system were included | Participants were patients with PBC who previously participated in a prospective epidemiological study. Most of them were recruited from Saint-Antoine hospital. Only patients who had liver histopathology available in the system were included. They were re-interviewed for this study in 2008 | Participants were patients with PBC who were seen at the University of Crete Medical School hospital, Greece. Only patients who had liver histopathology available in the system were included |
Second cohort: Patients with PBC who were seen at Cleveland Clinic in Cleveland, Ohio, from 1 January 1998 to 30 March 2006 were identified from the database of the hospital. Only patients who had liver histopathology available in the system were included | |||
Diagnosis of PBC | First cohort: Presence of ICD-9 code for PBC in the database plus 1. Detectable AMA, 2. Cholestatic biochemical profile ≥six months and 3. Compatible liver histology | Presence of at least two of the following criteria; 1. Cholestatic biochemical profile ≥six months, 2. presence of AMA or anti-gp210 ANA (titer ≥1:40 and detectable on ELISA) and 3. compatible liver histology | Based on standard biochemical, immunological, and histological criteria |
Second cohort: Same as the first cohort | |||
Determination of smoking status | First cohort: Data on smoking status were retrieved from health questionnaire filled by the patients during visits with healthcare providers of those hospitals. Second cohort: Same as the first cohort | Smoking status was determined through health questionnaires answered by the patients for this study. | Smoking status was determined through health questionnaires answered by the patients for this study. |
Definition of advanced fibrosis | First cohort: Stage of liver fibrosis was defined based on liver biopsy using Ludwig’s classification. Stage 3 and 4 were considered advanced fibrosis | Stage of liver fibrosis was defined based on liver biopsy using Ludwig’s classification. Stage 3 and 4 were considered advanced fibrosis | Stage of liver fibrosis was defined based on liver biopsy using Metavir-based classification system. F3 and F4 were considered advanced fibrosis |
Second cohort: Same as the first cohort | |||
Females (%) | First cohort: 87.6 | 90.2 | 86.5 |
Second cohort: 91.3 | |||
Average age (yr) | First cohort: 53.0 | 50.0 | 65.6 |
Second cohort: 52.0 | |||
Race (%) | First cohort: Caucasian (91.8) | NA | NA |
Second cohort: Caucasian (95.7) | |||
History of smoking (%) | First cohort: 51.0 | 26.0 | 32.7 |
Second cohort: 50.3 | |||
Patients with advanced liver fibrosis (%) | First cohort: 49.4 | 20.5 | 17.5 |
Second cohort: 51.5 | |||
Confounder adjusted in multivariate analysis | None | Sex and significant alcohol consumption | Sex and significant alcohol consumption |
Newcastle-Ottawa score | Selection: 3 | Selection: 3 | Selection: 3 |
Comparability: 1 | Comparability: 2 | Comparability: 2 | |
Exposure: 3 | Exposure: 3 | Exposure: 3 |
PBC, primary biliary cirrhosis; AMA, antimitochondrial antibody; ICD-9, international classification of diseases-9; ANA, antinuclear antibody; ELISA, enzyme-linked immunosorbent assay; BMI, body mass index; NA, not available