Skip to main content
Log in

Serum spermidine oxidase activity in patients with insulin-dependent diabetes mellitus and microvascular complications

  • Original Contributions
  • Published:
Acta diabetologia latina Aims and scope Submit manuscript

Summary

Metabolism of polyamines (spermidine and spermine) is known to be strictly related to the growth processes of eukaryotic cells. Since cell replication processes appear altered in insulin-dependent diabetes mellitus (IDDM), especially when associated with its microvascular complications, the aim of this study was measuring serum spermidine oxidase activity (SOA), a key enzyme in the metabolic pathway of polyamines, in 47 patients with IDDM as compared with 63 healthy control subjects matched for age and sex. Mean SOA levels±SD were significantly lower in IDDM patients (177.4±57.2 µkat/l) than in controls (247.6±68.1 µkat/l; p<0.001), being SOA inversely related with daily insulin dose. SOA was moreover significantly higher (but similar to controls) in the group with increased urinary albumin excretion rate (AER persistently >20 µg/min); (n=17; 213.1±62.6 µkat/l) in comparison with normoalbuminuric subjects (n=30; 156.6±43.5 µkat/l; F=21.78; p=0.0001). SOA was correlated with AER (r=0.45; p=0.001), independently of age, duration of disease, serum creatinine, body weight, blood pressure and metabolic control, as shown by a multiple regression analysis model (p=0.003). Presence of background retinopathy was not associated with modified levels of SOA, which was conversely higher, although not significantly, in the patients with proliferative retinal lesions. In conclusion serum SOA is deeply altered in IDDM patients, being markedly reduced in the whole group of patients and conversely independently increased up to the mean values of controls in presence of increased AER or advanced retinopathy.

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. Bending J. J., Lobo-Yeo A., Vergani D., Viberti G. C.: Proteinuria and activated T-lymphocytes in diabetic nephropathy — Diabetes37, 507–511, 1988.

    Article  PubMed  CAS  Google Scholar 

  2. Byrd J., Jacobs D. M., Amoss M. S.: Synthetic polyamines added to cultures containing bovine sera, reversibly inhibitin vitro parameters of immunity — Nature (Lond.)267, 621–623, 1977.

    Article  CAS  Google Scholar 

  3. Conover C. A., Rozovski S. J., Belur E. L., Aoki T. T., Ruderman N. B.: Ornithine decarboxylase activity in insulin-deficient states — Biochem. J.192, 725–732, 1980.

    PubMed  CAS  Google Scholar 

  4. Flayeh K. A.: Spermidine oxidase activity of normal and schizophrenic subjects — Clin. Chem.34, 401–403, 1988.

    PubMed  CAS  Google Scholar 

  5. Gahl A., Vale A. M., Pitot H. C.: Spermidine oxidase in human pregnancy serum — Biochem. J.201, 161–166, 1982.

    PubMed  CAS  Google Scholar 

  6. Gaugas M., Curzen P.: Polyamine interaction with pregnancy serum in suppression of lymphocyte transformation — Lanceti, 18–20, 1978.

    Article  Google Scholar 

  7. Groop L. C., Teir H., Koskimies S., Groop P. H., Matikainen E., Verkkala E., Scheinin T., Kontianen S., Teppo A. M., Tolppanen E. M., Tallgren L. G.: Risk factors and markers associated with proliferative retinopathy in patients with insulin-dependent diabetes — Diabetes35, 1397–1403, 1986.

    Article  PubMed  CAS  Google Scholar 

  8. Illei G., Morgan D. M. L.: Polyamine oxidase activity in human pregnancy serum — Brit. J. Obstet. Gynaecol.86, 878–881, 1979.

    CAS  Google Scholar 

  9. Janne J., Poso H., Raina A.: Polyamines in rapid growth and cancer — Biochim. biophys. Acta (Amst.)473, 241–293, 1970.

    Google Scholar 

  10. Mondovì B., Riccio P.: Animal intracellular amine oxidases. In:Mondoví B. (Ed.): Structure and Functions of Amine Oxidases. CRC Press, Boca Raton/FL, 1985; pp. 63–76.

    Google Scholar 

  11. Mondovì B., Riccio P., Agostinelli E.: The biological functions of amine oxidases and their reaction products: an overview. In:Zappia V., Pegg A. E. (Eds): Progress in Polyamine Research. Plenum Press, New York, 1988; pp. 147–171.

    Google Scholar 

  12. National Diabetes Data Group: Classification and diagnosis of diabetes mellitus and other categories of glucose intolerance — Diabetes28, 1039–1057, 1979.

    Google Scholar 

  13. Petty R. G., Pearson J. D., Morgan D. M. L., Mahler R. F.: Stimulation of endothelial cell growth by sera from diabetic patients with retinopathy — Lanceti, 208–211, 1988.

    Article  Google Scholar 

  14. SAS Institute Inc.: SAS/STAT Guide for Personal Computers. 6th Ed. SAS Institute Inc., Cary/NC, 1987.

    Google Scholar 

  15. Scheinen T., Groop L., Teir H., Koskimies S., Kontianen S.: HLA-types and insuline responses in insulin dependent diabetics with and without proliferative retinopathy — J. clin. Lab. Immunol.18, 17–20, 1985.

    Google Scholar 

  16. Trevisan R., Li K. L., Walker J. D., Viberti G. C.: Overactivity of Na+/H+ antiport and enhanced cell growth in fibroblasts of type 1 (insulin-dependent) diabetic patients with nephropathy — Diabetologia32, 549A, 1989.

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Seghieri, G., Gironi, A., Niccolai, M. et al. Serum spermidine oxidase activity in patients with insulin-dependent diabetes mellitus and microvascular complications. Acta diabet. lat 27, 303–308 (1990). https://doi.org/10.1007/BF02580934

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02580934

Key-words

Navigation