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Diabetes mellitus and some genetic markers
C.A.A. BarbosaI; L.M.C. KoberleIII; C.V. CaiadoI; J.C. PedrazzaniII; E.M. VignaliII; Y. LescuraII
IDepartamento de Ciências da Saúde, Universidade Federal de São Carlos, 13560 São Carlos, SP, Brasil. Send correspondence to C.A.A.B.
IIDepartamento de Enfermagem, Universidade Federal de São Carlos, 13560 São Carlos, SP, Brasil
IIIClínica São Lucas, Rua 15 de Novembro, 1688, 13560 São Carlos, SP, Brasil
ABSTRACT
The phenotypic distributions of some genetic markers [GLO, ESD, Hp, PGM, ABO, Rh] ' were studied in a sample of diabetes patients and in their normal relatives. A statistically significant association between the haptoglobin system and type II diabetes was detected. The relative risk of having type II diabetes was about 2.5 higher for Hp 2-2 individuals. However, since 12 tests of heterogeneity between groups were performed, it was expected that about one of them would be significant by chance alone. Therefore, the observed Hp association could be a result of a type I statistical error
Keywords: diabetes; mellitus; genetic; markers.
REFERENCES
Conceição, M.M., Salzano, F.S., Franco, M.H.L.P., Weimer, T. and Krieger, H. (1987). Demography, genetics, and race admixture in Aracaju, Brazil. Rev. Brasil. Genet. 10: 313-331.
Cudworth, A.G. and Woodwrow, J.C. (1975). HL-A system and diabetes mellitus. Diabetes 24: 345-349.
Franco, M.H.L.P., Salzano, F.M. and Maia de Lima, F.A. (1981). Blood groups and serum protein types in two brazilian populations. Rev. Brasil. Genet. 4: 689-704.
Hopkinson, D.A., Mestriner, M.A., Cortner, J. and Harris, H. (1973). Esterase D: a new human polymorphism. Ann. Hum. Genet. Lond. 37: 119-137.
Hopkinson, D.A., Coppock, J.S., Muhlemann, M.F. and Edwards, Y.H. (1974). The detection and differentiation of the products of the human carbonic anhydrase loci, CA I and Ca II, using fluorogenic substrates. Ann. Hum. Genet. Lond. 38: 155-162.
Kirk, R.L., Theophilus, J., Whitehouse, S., Court, J. and Zimmet, P. (1979). Genetic susceptibility to Diabetes Mellitus: the distribution of the Properdin Factor B (bf) and Glyoxalase (GLO) phenotypes. Diabetes 28: 949-951.
Mayo, O. (1978). Polymorphism, Selection and Evolution. In: The Biochemical Genetics of Man (Brock, D.J.H. and Mayo, O. eds.) Academic Press, London, pp. 157-183.
Moens, H., Payne, R., Carter, N.D. and Farid, N.R. (1980). Association of Glyoxalase I allotypes with Graves' disease and Diabetes mellitus. Hum. Hered. 30: 62-64.
Nerup, J., Platz, P., Anderson, O., Christy, M., Lyngsoe, J., Poulson, J., Ryder, L.P., Thomsen, M., Nielson, L.S. and Svejgaard, A. (1974). HLA antigens and diabetes mellitus. Lancet II: 864866.
Parr, C.W., Bagster, I. and Welch, S.G. (1977). Human red cell glyoxalase I polymorphism. Biochem. Genet. 15: 109-113.
Raum, D., Ayer, C.A., Stein, R. and Gabbay, K.H. (1979). Genetic marker for insulin-dependent diabetes mellitus. Lancet I: 1208-1210.
Smithies, O. (1955). Zone electrophoresis in starch gels: group variation in the serum protein of normal human adults. Biochem. J. 61: 629-641.
Spencer, N., Hopkinson, D.A. and Harris, H. (1964). Phosphoglucomutase polymorphism in man. Nature 204: 742-745.
Woolf, B. (1955). On estimating the relation between blood group and disease. Ann. Hum. Genet. Lond. 19: 251-253.