Skip to main content
Log in

Chromosome abnormalities in peripheral lymphocytes from patients with progressive systemic sclerosis

  • Originals
  • Published:
Rheumatology International Aims and scope Submit manuscript

Summary

Chromosomal abnormalities in cultured peripheral lymphocytes from 14 progressive systemic sclerosis (PSS) patients and 15 normal subjects were examined. No increase was observed in the frequency of chromosome aberrations in PSS patients who had not received any medical treatment. Those who had received medication showed an increased frequency of dicentrics (0.3%) although the frequency was not significantly higher than that for normal subjects. It is not clear, however, whether the increase was due to the hypersensitivity of PSS patients to agents used for therapeutic purposes.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Emerit I, Housset E, Grouchy J de, Camus JP (1971) Chromosomal breakage in diffuse scleroderma: a study of 27 patients. Rev Eur Etud Clin Biol 16:684–694

    Google Scholar 

  2. Pan SF, Rodnan GP, Deutsch M, Wald N (1975) Chromosomal abnormalities in progressive systemic sclerosis (scleroderma) with consideration of radiation effects. J Lab Clin Med 86:300–308

    Google Scholar 

  3. Sherer GK, Jackson BB, Leroy EC (1981) Chromosome breakage and sister chromatid exchange frequencies in scleroderma. Arthritis Rheum 24:1409–1413

    Google Scholar 

  4. Powell FC, Schroeter AL, Winkelmann RK, Dewald GW (1986) Chromosome studied in scleroderma with consideration of anti-centromere antibody status and assessment of possible in vitro clastogenic activity. Acta Derm Venereol (Stockh) 66:414–418

    Google Scholar 

  5. Wolff DJ, Needleman BW, Wasserman S, Schwartz S (1991) Spontaneous and clastogen induced chromosomal breakage in scleroderma. J Eheumatol 18:837–840

    Google Scholar 

  6. Romani F, Viguie F, Siffroi JP, Fiessenger JN (1986) A cytogenic analysis of twenty cases of systemic scleroderma. Ann Genet 29:240–245

    Google Scholar 

  7. Emerit I, Housset E, Feingold I (1976) Chromosomal breakage and scleroderma: studied in family members. J Lab Clin Med 88:81–86

    Google Scholar 

  8. Rittner G, Schwantz G, Baur MP, Black CM, Welsh KI, Kuhnl P, Rittner C (1988) Family studies in scleroderma (systemic sclerosis) demonstrating in HLA-linked increased chromosomal breakage in rate in cultured lymphocytes. Hum Genet 81:64–70

    Google Scholar 

  9. Talbott JH, Barrocas M (1979) Progressive systemic sclerosis (PSS) and malignancy, pulmonary and non-pulmonary. Medicine 58:182–207

    Google Scholar 

  10. Peters-Golden M, Wise RA, Hochberg M, Stevens MB, Wigley FM (1985) Incidence of lung cancer in systemic sclerosis. J Rheumatol 12:1136–1139

    Google Scholar 

  11. Auclair C, Gouyette A, Levy A, Emerit I (1990) Clastogenic inosine nucleotide as components of the chromosome breakage factor in scleroderma patients. Arch Biochem Biophys 278:238–244

    Google Scholar 

  12. Palmer RG, Pereira RS, Dore CJ, Denman AM (1986) Sister chromatid exchange frequencies in patients with scleroderma and their relatives. Ann Rheum Dis 45:409–411

    Google Scholar 

  13. Hirai M, Omoto K, Tanaka H, Hisawa S, Mercado AS, Pagaran IG, Eviota W (1986) Chromosome aberrations in leukocytes of filaria-infected indigenous inhabitants in the Philippines Jpn J Exp Med 56:285–291

    Google Scholar 

  14. Maeda H, Takeuchi F, Juji T, Akanuma Y, Kasuga M, Lee YS, Kosaka K, Tsai SH (1980) HLA-DRw3 in juvenile on set diabetes mellitus in Chinese. Tissue Antigens 15:173–176

    Google Scholar 

  15. Bein G, Gläser R, Kirchner H (1992) Rapid HLA-DRB1 genotyping by nested PCR amplification. Tissue Antigens 39:68–73

    Google Scholar 

  16. Yamada H, Nakano K, Takeuchi F, Matsuta K, Hong G, Itoh K, Tokunaga K, Kuwata S, Tanimoto K (1991) C4 and HLADR typing in Japanese patients with SLE (abstr) (in Japanese). Proc J Soc Immunol 21:231

    Google Scholar 

  17. Tonomura A, Kishi K, Saito F (1983) Types and frequencies of chromosome aberrations in peripheral lymphocytes of general populations. In: Ishihara T (ed) Radiation-induced chromosome damage in man. Liss, New York, pp 605–616

    Google Scholar 

  18. Emerit I (1980) Chromosomal instability in collagen disease. Z Rheumatol 39:84–90

    Google Scholar 

  19. Moroi Y, Takeuchi A, Chihara T, Tanimoto K, Hirose S, Murata K, Maeda H, Takehara K, Yokohari R (1982) HLA antigens in patients with progressive systemic sclerosis (in Japanese). In: Annual Report of the Ministry of Health and Welfare Scleroderma Research Committee, Tokyo, 1981, pp 66–70

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Takeuchi, F., Nakano, K., Yamada, H. et al. Chromosome abnormalities in peripheral lymphocytes from patients with progressive systemic sclerosis. Rheumatol Int 12, 243–246 (1992). https://doi.org/10.1007/BF00301010

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00301010

Key words

Navigation