Abstract
A group of 100 totally or subtotally myeloperoxidase (MPO)-deficient individuals was compared to a reference population of 118 probands selected at random. Data for a protective effect of the deficiency against cardiovascular damage are presented. On the other hand, a significantly higher occurrence of severe infections and chronic inflammatory processes was noted among the deficient patients. An increased incidence of cancer among the MPO-deficient individuals was not demonstrated.
References
1.
Jolivalt C, Leininger-Muller B, Drozdz R, Nakasalski JW, Siest G: Apolipoprotein E is highly susceptible to oxidation by myeloperoxidase, an enzyme present in the brain. Neurosci Lett 1996;210:61–64.
2.
Lehrer RI, Cline MJ: Leukocyte myeloperoxidase deficiency and disseminated candidiasis. J Clin Invest 1969;48:1478–1488.
3.
Proceedings of the Symposium Recent Developments in Myeloperoxidase Deficiency, Luxembourg, Oct 1996. J Mol Med 1998:76:659–698.
4.
2nd International Conference on the Peroxidase Family. Fraueninsel-Lake Chiemsee, Sept/Oct 1998.
5.
Lanza F, Musto P, Franzè D: Hereditary myeloperoxidase deficiency syndrome. Ital J Med 1985;1:45–52.
6.
Lanza F, Fietta A, Spisani S, Castoldi GL, Traniello S: Does a relationship exist between neutrophil myeloperoxidase deficiency and the occurrence of neoplasms? J Clin Lab Immunol 1987;22:175–180.
7.
Lanza F, Giuliani A L, Amelotti F, Spisani S, Traniello S, Castoldi GL: Depressed neutrophil-mediated tumor cell cytotoxicity in subjects affected by hereditary myeloperoxidase deficiency and secondary neoplasia. Haematologia 1988;72:355–358.
8.
Kutter D, Al Haidari K, Thoma J: Myeloperoxidase deficiency: Simple methods for its diagnosis and significance of different forms. Klin Lab 1994;40:342–346.
9.
Heinecke JW: Mechanisms of oxidative damage by myeloperoxidase in atherosclerosis and other inflammatory diseases. J Lab Clin Med 1999;133:321–325.
10.
Larrocha C, Fernandez de Castro M, Fontan G, Viloria A, Fernandez-Chacon JL, Jimenez C: Hereditary myeloperoxidase deficiency: Study of 12 cases. Scand J Haematol 1982;29:389–397.
11.
Davis AT, Brunning RD, Quie PC: Polymorphonuclear leukocyte myeloperoxidase deficiency in a patient with myelomonocytic leukemia. N Engl J Med 1971;285:789–790.
12.
Cech P, Papathanassiou A, Boreux G, Roth P, Miescher PA: Hereditary myeloperoxidase deficiency. Blood 1979;53:403–411.
13.
Bos AJ, Weening RS, Hamers MN, Wever R, Behrendt H, Roos D: Characterization of hereditary partial myeloperoxidase deficiency. J Lab Clin Med 1979;99:589–600.
14.
Ross WD: Totale Myeloperoxidasedeficienz. Blutbild Atlas. Munich, Bayer Diagnostics, 1993.
15.
Huhn D, Belhohradsky BH, Haas R: Familiärer Myeloperoxidasedefekt und akute myeloische Leukämie. Acta Haematol1978;59:129–143.
16.
Parry MF, Root RK, Metcalf JA, Delaney KK, Kaplow LS, Richar WJ: Myeloperoxidase deficiency. Ann Intern Med 1981;95:293–301.
17.
Nauseef WM, Root RK, Malech HL: Biochemical and immunologic analysis of hereditary myeloperoxidase deficiency. J Clin Invest 1983;71:1297–1307.
18.
Dri P, Cramer R, Soranzo MR, Comin A, Miotti V, Patriarca P: New approaches to the detection of myeloperoxidase deficiency. Blood 1982;60:323–327.
19.
Moosmann K, Bojanovsky A: Rezidivierende Candidosis bei Myeloperoxidasemangel. Monatsschr Kinderheilk 1975;123:408–409.
20.
Undritz E: Die Alius-Grignaschi-Anomalie: Der erblich-konstitutionelle Peroxydasedefekt der Neutrophilen und der Monozyten. Blut 1966;14:129–136.
21.
Grignaschi VJ, Sperperato AM, Eetcheverry MJ, Macario AJL: Un nuevo quadro citoquimi- co: Negatividad espontanea de las recciones de peroxidasas, oxidasas y lipido en la progenia neutrofila y en los monocitos de dos hermanos. Rev Assoc Med Argent 1963;77:218.
22.
Tobler A, Selsted ME, Miller CW, Johnson KR, Novotny MJ, Rovera G, Koeffler HP: Evidence for a pretranslational defect in hereditary and acquired myeloperoxidase deficiency. Blood 1989;73:1986–1989.
23.
Gerber CE, Kuçi S, Zipfel M, Niethammer D, Bruchelt G: Phagocytic activity and oxidative burst of granulocytes in persons with myeloperoxidase deficiency. Eur J Clin Chem Clin Biochem 1996;34:901–908.
© 2000 S. Karger AG, Basel
2000
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