Serum bilirubin: a prognostic factor in primary biliary cirrhosis
Open accessAbstract
We followed up 55 patients with proven primary biliary cirrhosis for several years or until death. A graph of the level of serum bilirubin versus time that was constructed for each patient shows an initial period of variable length in which the serum bilirubin level remained constant. This was followed by a period of rapid rise in serum bilirubin which culminated in the patient's death. Whenever two successive serum bilirubin values taken six months apart exceeded 34 mumol/l (2.0 mg/dl) the patient had entered a late phase of disease and lived an average of 49 months. Ninety-five per cent confidence limits on survival time were 32-74 months. If two successive six month bilirubin values exceeded 102 mumol/l (6.0 mg/dl), calculated survival time was 25 months, and if two successive six month bilirubin values exceeded 170 mumol/l (10.0 mg/dl), survival time was 17 months. Fifteen of the 41 living patients had two consecutive serum bilirubin levels greater than 34 mumol/l (2.0 mg/dl). However, the slope of the rising bilirubin in the living patients is only 35 mumol/l/yr (1.5 mg/dl/yr) compared with 42 mumol/l/yr (2.5 mg/dl/yr) in the dead patients. This means that patients with this disease not may be living considerably longer.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Mean survival once the bilirubin is 34 μmol/L is 4 years, and when the bilirubin reaches 102 μmol/L mean survival is only 2 years.
“mean survival once the bilirubin is 34 μmol/L is 4 years, and when the bilirubin reaches 102 μmol/L mean survival is only 2 years.132”
From The British Society of Gastroenterology/UK-PBC primary biliary cholangitis treatment and management guidelines (2018) · cites this paper as [132]
The Presentation table reports geometric mean survival of 49 months above 34 μmol/L and 25 months above 102 μmol/L, approximately four and two years. But these estimates apply after two successive bilirubin measurements six months apart exceed the thresholds, not when a single measurement reaches them; the Discussion reiterates this condition. Page numbers are not provided in the supplied passages. (LLM, conf=0.88)
Experimental — accuracy not yet measuredSerum bilirubin has been recognized since the 1970s as a major predictor of poor PBC outcome.
“Serum bilirubin has been recognised since the 1970s as a major predictor of poor outcome in PBC [72,7].”
From EASL Clinical Practice Guidelines: The diagnosis and management of patients with primary biliary cholangitis. (2017) · cites this paper as [72]
Serum bilirubin has been recognised since the 1970s as a major predictor of poor outcome in PBC.
“Serum bilirubin has been recognised since the 1970s as a major predictor of poor outcome in PBC [72,7].”
From EASL Clinical Practice Guidelines: The diagnosis and management of patients with primary biliary cholangitis. (2017) · cites this paper as [72]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
(2008) · International Union of Pure and Applied Chemistry (IUPAC) eBooks · doi:10.1351/goldbook.l03614 · Cited by 1,792 · see citing works
Krendel, E. S. (1957) · Journal of the Franklin Institute · doi:10.1016/0016-0032(57)90869-4 · Cited by 385 · see citing works
PRIMARY BILIARY CIRRHOSIS. CHRONIC NON-SUPPURATIVE DESTRUCTIVE CHOLANGITIS.
Rubin, E., Schaffner, F., & Pópper, H. (1965) · PubMed · Cited by 375 · see citing works
Self-citationCopper Metabolism in Normal Subjects
Cartwright, G. E., & Wintrobe, M. M. (1964) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/14.4.224 · Cited by 265 · see citing works
Acute copper sulfate poisoning
Chuttani, H. K., Gupta, P., Gulati, S., et al. (1965) · The American Journal of Medicine · doi:10.1016/0002-9343(65)90105-1 · Cited by 208 · see citing works
Tuberculosis of bones and joints
Girdlestone, G. R., & Capener, N. (1924) · British Journal of Tuberculosis · doi:10.1016/s0366-0850(24)80055-8 · Cited by 172 · see citing works
IS PRIMARY BILIARY CIRRHOSIS AN IMMUNE COMPLEX DISEASE?
Thomas, H. C., Potter, B. J., & Sherlock, S. (1977) · The Lancet · doi:10.1016/s0140-6736(77)92666-6 · Cited by 121 · see citing works
A CONTROLLED TRIAL OF D-PENICILLAMINE THERAPY IN PRIMARY BILIARY CIRRHOSIS
Jain, S., Samourian, S., Scheuer, P. J., et al. (1977) · The Lancet · doi:10.1016/s0140-6736(77)92778-7 · Cited by 96 · see citing works
Relation Between Cirrhosis and Trace Metal Content of Liver
Hunt, A. H., Parr, R. M., Taylor, D. M., et al. (1963) · BMJ · doi:10.1136/bmj.2.5371.1498 · Cited by 93 · see citing works
Evolution of the hepatic lesion in Wilson's disease (hepatolenticular degeneration).
Sternlieb, I. (1972) · PubMed · Cited by 70 · see citing works
Effect of d-Penicillamine on Copper Retention in Patients with Primary Biliary Cirrhosis
Deering, T. B., Dickson, E. R., Fleming, C. R., Geall, M. G., McCall, J., & Baggenstoss, A. H. (1977) · Gastroenterology · doi:10.1016/s0016-5085(77)80012-7 · Cited by 67 · see citing works
Effect of D-penicillamine on copper retention in patients with primary billiary cirrhosis.
Deering, T. B., Dickson, E. R., Fleming, C. R., Geall, M. G., McCall, J., & Baggenstoss, A. H. (1977) · PubMed · Cited by 65 · see citing works
Studies on Chronic Copper Poisoning: I. Toxicity of Copper Sulphate and Copper Acetate in Sheep
Todd, J. R., Gracey, J. F., & Thompson, R. H. (1962) · British Veterinary Journal · doi:10.1016/s0007-1935(17)42754-0 · Cited by 32 · see citing works
Problems of disabled students.
Gunn, A. D. (1976) · BMJ · doi:10.1136/bmj.2.6050.1498 · Cited by 6 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Hirschfield, G. M., Beuers, U., Corpechot, C., Invernizzi, P., Jones, D., Marzioni, M., & Schramm, C. (2017) · Journal of Hepatology · doi:10.1016/j.jhep.2017.03.022 · Cited by 1,480 · see citing works
Carey, E. J., Ali, A. H., & Lindor, K. D. (2015) · The Lancet · doi:10.1016/s0140-6736(15)00154-3 · Cited by 735 · see citing works
Biochemical response to ursodeoxycholic acid and long-term prognosis in primary biliary cirrhosis
Corpechot, C., Abenavoli, L., Rabahi, N., Chrétien, Y., Andréani, T., Johanet, C., Chazouillères, O., & Poupon, R. (2008) · Hepatology · doi:10.1002/hep.22428 · Cited by 646 · see citing works
Hirschfield, G. M., Mason, A., Luketic, V., Lindor, K., Gordon, S. C., Mayo, M., Kowdley, K. V., Vincent, C., Bodhenheimer, H. C., Parés, A., et al. (2015) · Gastroenterology · doi:10.1053/j.gastro.2014.12.005 · Cited by 576 · see citing works
Lammers, W. J., van Buuren, H. R., Hirschfield, G. M., Janssen, H. L. A., Invernizzi, P., Mason, A. L., Ponsioen, C. Y., Floreani, A., Corpechot, C., Mayo, M. J., et al. (2014) · Gastroenterology · doi:10.1053/j.gastro.2014.08.029 · Cited by 498 · see citing works
Lammers, W. J., Hirschfield, G. M., Corpechot, C., Nevens, F., Lindor, K. D., Janssen, H. L. A., Floreani, A., Ponsioen, C. Y., Mayo, M. J., Invernizzi, P., et al. (2015) · Gastroenterology · doi:10.1053/j.gastro.2015.07.061 · Cited by 441 · see citing works
Roll, J., Boyer, J. L., Barry, D., & Klatskin, G. (1983) · New England Journal of Medicine · doi:10.1056/nejm198301063080101 · Cited by 417 · see citing works
Hirschfield, G. M., Dyson, J. K., Alexander, G. J. M., Chapman, M. H., Collier, J., Hübscher, S., Patanwala, I., Pereira, S. P., Thain, C., Thorburn, D., et al. (2018) · Gut · doi:10.1136/gutjnl-2017-315259 · Cited by 347 · see citing works
Goulis, J., Leandro, G., & Burroughs, A. K. (1999) · The Lancet · doi:10.1016/s0140-6736(98)11293-x · Cited by 315 · see citing works
Opioid peptides and primary biliary cirrhosis
Thornton, J. R., & Losowsky, M. S. (1988) · BMJ · doi:10.1136/bmj.297.6662.1501 · Cited by 300 · see citing works
Bacteriuria and primary biliary cirrhosis.
Burroughs, A. K., Rosenstein, I. J., Epstein, O., Hamilton-Miller, J. M., Brumfitt, W., & Sherlock, S. (1984) · Gut · doi:10.1136/gut.25.2.133 · Cited by 214 · see citing works
Hyperlipidaemic state and cardiovascular risk in primary biliary cirrhosis
Longo, M., Crosignani, A., Battezzati, P. M., Squarcia Giussani, C., Invernizzi, P., Zuin, M., & Podda, M. (2002) · Gut · doi:10.1136/gut.51.2.265 · Cited by 190 · see citing works
Angulo, P., Jorgensen, R. A., Keach, J. C., Dickson, R. E., Smith, C., & Lindor, K. D. (2000) · Hepatology · doi:10.1002/hep.510310209 · Cited by 179 · see citing works
Correlation of initial autoantibody profile and clinical outcome in primary biliary cirrhosis
Wesierska-Gadek, J., Penner, E., Battezzati, P. M., Selmi, C., Zuin, M., Hitchman, E., Worman, H. J., Gershwin, E. M., Podda, M., & Invernizzi, P. (2006) · Hepatology · doi:10.1002/hep.21172 · Cited by 177 · see citing works
Randomized trial of chlorambucil for primary biliary cirrhosis
Hoofnagle, J. H., Davis, G. L., Schafer, D. F., Peters, M., Avigan, M. I., Pappas, S. C., Hanson, R. G., Minuk, G. Y., Dusheiko, G. M., Campbell, G., et al. (1986) · Gastroenterology · doi:10.1016/0016-5085(86)90183-6 · Cited by 157 · see citing works
Diminished survival in asymptomatic primary biliary cirrhosis
Balasubramaniam, K., Grambsch, P. M., Wiesner, R. H., Lindor, K. D., & Dickson, E. R. (1990) · Gastroenterology · doi:10.1016/0016-5085(90)91091-j · Cited by 141 · see citing works
Natural history of primary biliary cirrhosis
Parés, A., & Rodés, J. (2003) · Clinics in Liver Disease · doi:10.1016/s1089-3261(03)00100-4 · Cited by 89 · see citing works
Silveira, M. G., Brunt, E. M., Heathcote, J., Gores, G. J., Lindor, K. D., & Mayo, M. J. (2010) · Hepatology · doi:10.1002/hep.23637 · Cited by 87 · see citing works
Symptom development and prognosis in primary biliary cirrhosis: a study in two centers
Mitchison, H. C., Lucey, M. R., Kelly, P. J., Neuberger, J. M., Williams, R., & James, O. F. W. (1990) · Gastroenterology · doi:10.1016/0016-5085(90)90968-7 · Cited by 74 · see citing works
Poupon, R. E., Balkau, B., Guéchot, J., & Heintzmann, F. (1994) · Hepatology · doi:10.1002/hep.1840190314 · Cited by 58 · see citing works
Weber, P., Brenner, J., Stechemesser, E., Klein, R., Weckenmann, U., Klöppel, G., Kirchhof, M., Fintelmann, V., & Berg, P. A. (1986) · Hepatology · doi:10.1002/hep.1840060402 · Cited by 50 · see citing works
Angulo, P., Jorgensen, R. A., & Lindor, K. D. (2001) · The American Journal of Gastroenterology · doi:10.1111/j.1572-0241.2001.05270.x · Cited by 39 · see citing works
Utility of Noninvasive Markers of Fibrosis in Cholestatic Liver Diseases
Corpechot, C. (2016) · Clinics in Liver Disease · doi:10.1016/j.cld.2015.08.013 · Cited by 19 · see citing works
Heathcote, J. E., Cauch-Dudek, K., Walker, V., Bailey, R. J., Blendis, L. M., Ghent, C. N., Michieletti, P., Minuk, G. Y., Pappas, C. S., Scully, L. J., et al. (1994) · Hepatology · doi:10.1002/hep.1840190512 · Cited by 2 · see citing works
- Authors
- Shapiro, J. M., Smith, H., & Schaffner, F.
- Affiliations
- City University of New York (US)
- Venue
- Gut
- Publisher
- BMJ
- Published
- 1979-02
- Volume
- 20
- Issue
- 2
- Pages
- 137-140
- ISSN
- 0017-5749 (ISSN-L)
- 1468-3288
- PMC
- PMC1419455
- OpenAlex
- W1975579398
- Semantic Scholar
- 5db469a0030e3c8b406982f871318edde62e9b2a
- Cited by
- 319
- References
- 14
- Citations by year
- 2026: 6 · 2025: 5 · 2024: 5 · 2023: 7 · 2022: 2 · 2021: 6 · 2020: 7 · 2019: 4 · 2018: 6 · 2017: 6 · 2016: 5 · 2015: 12 · 2014: 6 · 2013: 2 · 2012: 8
- FWCI
- 5.73
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Gut (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Hepatology › Liver Diseases and Immunity
- Health Sciences › Medicine › Surgery › Pediatric Hepatobiliary Diseases and Treatments
- Health Sciences › Medicine › Hepatology › Liver Disease and Transplantation
- Keywords
- primary biliary cirrhosis, serum bilirubin, prognostic factors, survival time, disease progression, bilirubin kinetics, mortality
- MeSH terms
- Adult, Aged, Bilirubin, Female, Follow-Up Studies, Humans, Liver Cirrhosis, Biliary, Male, Middle Aged, Prognosis
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review