Literature DB >> 1699877

Chromosomal aberrations in patients with primary biliary cirrhosis.

A Notghi1, U Nestle, G Rittner, P Brissot, H Jouanolle, M Manns, E Schleiermacher, C Rittner.   

Abstract

Chromosomal aberrations in untreated lymphocyte cultures, bleomycin (BLM)-induced aberrations and sister chromatid exchanges (SCE) in the peripheral blood lymphocytes of 11 patients suffering from primary biliary cirrhosis (PBC) and 14 matched control individuals were analysed. The lymphocytes of the PBC patients had on average a lower mitotic index (2.3) compared with controls (3.5) in the untreated cultures. The mean baseline rate of aberrations of the cultured lymphocytes of the patients was 5.3 aberrations per 100 metaphases (%); this was significantly different (P = 0.0291) from that of the controls with a mean of 2.3%. In lymphocytes of the patients and controls, most of the aberrations observed took the form of gaps; there was an almost equal breakage rate in both groups (0.5% and 0.4%, respectively). The average number of mitoses with aberrations in the PBC patients studied was double that of the controls (4.9% and 2.3% respectively, P = 0.0323). The mean number of the BLM-induced aberrations was 54.0% and 27.7% for the lymphocytes of the patients and controls, respectively. The mean number of the aberrant mitoses in the BLM cultures was 6 times higher than that of the untreated cultures for both groups, 25.7% and 14.6% respectively (P = 0.018). The chromosomal distribution of baseline and induced aberrations was not random. The PBC patients had a mean number of 8.7 SCE per mitosis, which was significantly higher than the SCEs in the controls (6.3 SCE per mitosis; P = 0.0156). The evidence suggests that the chromosomes of the lymphocytes of PBC patients may be less stable than those of the control individuals in this study.

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Year:  1990        PMID: 1699877     DOI: 10.1007/bf00194235

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  15 in total

1.  Chromosomal breakage and scleroderma: studies in family members.

Authors:  I Emerit; E Housset; J Feingold
Journal:  J Lab Clin Med       Date:  1976-07

2.  Two different subtypes of antimitochondrial antibodies are associated with primary biliary cirrhosis: identification and characterization by radioimmunoassay and immunoblotting.

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3.  A high susceptibility of Fanconi's anemia to chromosome breakage by DNA cross-linking agents.

Authors:  M S Sasaki; A Tonomura
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4.  Family studies in scleroderma (systemic sclerosis) demonstrating an HLA-linked increased chromosomal breakage rate in cultured lymphocytes.

Authors:  G Rittner; G Schwanitz; M P Baur; C M Black; K I Welsh; P Kühnl; C Rittner
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

5.  Variation in the expression of aphidicolin-induced fragile sites in human lymphocyte cultures.

Authors:  A P Craig-Holmes; L C Strong; A Goodacre; S Pathak
Journal:  Hum Genet       Date:  1987-06       Impact factor: 4.132

6.  Primary biliary cirrhosis: an increased incidence of extrahepatic malignancies?

Authors:  P R Mills; P Boyle; E M Quigley; G G Birnie; F Jarrett; G Watkinson; R N MacSween
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7.  Sister chromatid exchanges in patients with precancerous and cancerous lesions of cervix uteri.

Authors:  V V Murty; A B Mitra; U K Luthra; I P Singh
Journal:  Hum Genet       Date:  1986-01       Impact factor: 4.132

8.  Family study of the major histocompatibility complex in patients with systemic lupus erythematosus: importance of null alleles of C4A and C4B in determining disease susceptibility.

Authors:  A H Fielder; M J Walport; J R Batchelor; R I Rynes; C M Black; I A Dodi; G R Hughes
Journal:  Br Med J (Clin Res Ed)       Date:  1983-02-05

9.  Partial C4 deficiency in subacute sclerosing panencephalitis.

Authors:  C Rittner; E M Meier; B Stradmann; C M Giles; R Köchling; E Mollenhauer; H W Kreth
Journal:  Immunogenetics       Date:  1984       Impact factor: 2.846

10.  Breast cancer in women with primary biliary cirrhosis.

Authors:  B M Goudie; A D Burt; P Boyle; G Macfarlane; G G Birnie; P R Mills; C R Gillis; R N MacSween; G Watkinson
Journal:  Br Med J (Clin Res Ed)       Date:  1985-12-07
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