Content of reduced glutathione and consequences in recipients of glucose-6-phosphate dehydrogenase deficient red blood cells

American Journal of Hematology

Volumn 57, Issue 3, 1998, Pages 187-192

  Huang, Ching Shan ^a   Sung, Yung Chan ^a   Huang, May Jen ^a   Yang, Chung Shi ^c   Shei, Wei Shang ^a   Tang, Tang K ^b  

^a CATHAY GENERAL HOSPITAL   (Taiwan)

^b INSTITUTE OF BIOMEDICAL SCIENCES   (Taiwan)

^c TAICHUNG VETERANS GENERAL HOSPITAL   (Taiwan)

Author keywords

G6PD deficiency; Posttransfusional hemolysis reaction; Reduced glutathione

Indexed keywords

BILIRUBIN; DNA; GLUCOSE 6 PHOSPHATE DEHYDROGENASE; GLUTATHIONE; HAPTOGLOBIN; HEMOGLOBIN;

ANEMIA; ARTICLE; BLOOD DONOR; CLINICAL ARTICLE; CONTROLLED STUDY; ENZYME ACTIVITY; ERYTHROCYTE TRANSFUSION; GASTROINTESTINAL HEMORRHAGE; GENE MUTATION; GLUCOSE 6 PHOSPHATE DEHYDROGENASE DEFICIENCY; HEMATOCRIT; HEMOLYSIS; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; POSTOPERATIVE HEMORRHAGE; PRIORITY JOURNAL; TAIWAN;

ADULT; BILIRUBIN; BLOOD DONORS; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; DNA MUTATIONAL ANALYSIS; DNA PRIMERS; ERYTHROCYTE TRANSFUSION; ERYTHROCYTES; GLUCOSEPHOSPHATE DEHYDROGENASE; GLUCOSEPHOSPHATE DEHYDROGENASE DEFICIENCY; GLUTATHIONE; HAPTOGLOBINS; HEMATOCRIT; HEMOGLOBINOMETRY; HEMOLYSIS; HUMANS; TIME FACTORS;

EID: 0031909194     PISSN: 03618609     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8652(199803)57:3<187::AID-AJH1>3.0.CO;2-R     Document Type: Article

References (26)

1. Beutler E: G6PD deficiency. Blood 84:3613-3636, 1994.
2. Mimouni F, Shohat S, Reisner SH: G6PD-deficient donor blood as a cause of hemolysis in two preterm infants. Isr J Med Sci 22:120-122, 1986.
3. Kumar P, Sarkar S, Narang A: Acute intravascular hemolysis following exchange transfusion with G6PD deficient blood. Eur J Pediatr 153:98-99, 1994.
4. Gulati S, Singh S, Narang A, Bhakoo ON: Exchange transfusion with G6PD deficient donor blood causes exaggeration of neonatal hyperbilirubinemia. Ind Pediatr 26:499-501, 1989.
5. Orlina AR, Josephson AM, McDonald BJ: The poststorage viability of glucose-6-phosphate dehydrogenase deficiency erythrocyte. J Lab Clin Med 75:934-936, 1970.
6. Shalev O, Manny N, Sharon R: Posttransfusional hemolysis in recipients of glucose-6-phosphate dehydrogenase deficient erythrocyte. Vox Sang 14:94-98, 1993.
7. Shalev O, Bogomolski-Yahalom V, Sharon R: Hemolysis following transfusion of erythrocytes from a donor with G6PD deficiency and beta-thalassemia minor. Isr J Med Sci 29:214-216, 1993.
8. Yu MW, Hsiao KJ, Wuu KD, Chen CJ: Association between glucose-6-phosphate dehydrogenase deficiency and neonatal jaundice: Interaction with multiple risk factors. Int J Epidemiol 21:947-952, 1992.
9. Tang TK, Huang CS, Huang MJ, Tam KB, Yeh CH, Tang CJC: Diverse point mutations result in glucose-6-phosphate dehydrogenase (G6PD) polymorphism in Taiwan. Blood 79:2135-2140, 1992.
10. Huang CS, Hung KL, Huang MJ, Li YC, Liu TH, Tang TK: Neonatal jaundice and molecular mutations in glucose-6-phosphate dehydrogenase deficient newborn infants. Am J Hematol 51:19-25, 1996.
11. Chang JG, Chiou SS, Pergn LI, Chen TC, Liu TC, Lee LS, Chen PH, Tang TK: Molecular characterization of G6PD deficiency by natural and amplification created restriction sites: Five mutations account for most G6PD deficiency cases in Taiwan. Blood 80:1079-1082, 1992.
12. Chiu DTY, Zuo L, Chao L, Chen E, Louie E, Lubin B, Liu TZ, Du CS: Molecular characterization of glucose-6-phosphate dehydrogenase (G6PD) deficiency in patients of Chinese descent and identification of new base substitutions in the human G6PD gene. Blood 81:2150-2154, 1993.
13. Lo YS, Lu CC, Chiou SS, Chen BH, Chang TT, Chang JG: Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Chinese infants with or without severe neonatal hyperbilirubinemia. Br J Hematol 86:858-862, 1993.
14. Tang TK, Yeh CH, Huang CS, Huang MJ: Expression and biochemical characterization of human glucose-6-phosphate dehydrogenase in Escherichia coli: A system to analyze normal and mutant enzyme. Blood 83:1436-1441, 1994.
15. Chen HL, Huang MJ, Huang CS, Tang TK: G6PD Nankang (517 T → C; 173 Phe → Leu): A new G6PD variant identified in a Chinese associated with neonatal jaundice. Hum Hered 46:201-204, 1996.
16. Huang CS, Chen TH, Wei C, Chien TY, Jang JF: The clinical application of glucose-6-phosphate dehydrogenase quantitation test. J Formosan Med Assoc 81:938-944, 1982.
17. Yang CS, Chou ST, Liu L, Tsai PJ, Kuo JS: Effect of aging on human plasma glutathione concentrations as determined by high-performance liquid chromatography with fluorimetric detection. J Chromatogr 674: 23-30, 1995.
18. Chen HL, Liu TH, Huang MJ, Huang CS, Tang TK: Two novel glucose-6 phosphate dehydrogenase deficiency mutations and association of such mutations with F8C/G6PD haplotype in Chinese. J Formosan Med Assoc 1997 (in press).
19. Wolle LC: Oxidative injuries to the red cell membrane during conventional blood preservation. Sem Hematol 26:307-312, 1989.
20. Beutler E, Dern RJ, Flanagan CL, Alving AS: The hemolytic effect of primaquine: VII. biochemical studies of drug-sensitive erythrocytes. J Lab Clin Med 45:286-295, 1955.
21. Al-Ali AK: Erythrocyte reduced glutathione level in sickle cell anemia and glucose-6-phosphate dehydrogenase deficient Saudi subjects. Ann Clin Biochem 31:296-297, 1994.
22. McMurdy PR, Morse EE: Glucose-6-phosphate dehydrogenase deficiency and blood transfusion. Vox Sang 28:230-237, 1975.
23. Kuhn VL, Lisboa V, de Cerqueira LP: Glucose-6-phosphate dehydrogenase in blood donors in a general hospital of Salvador, Bahia, Brazil. Rev Paul Med 101:175-177, 1983.
24. Kurdi-Haidar B, Mason PJ, Berrebi A, Ankra-Badu G, Al-Ali A, Oppenheim A, Luzzatto L: Origin and spread of the glucose-6-phosphate dehydrogenase variant (G6PD-Mediterranean) in the Middle East. Am J Hum Genet 47:1013-1019, 1990.
25. Ragusa R, Cataldo AD, Gangarossa S, Nigro LL, Schiliro G: Low grade hemolysis and assessment of iron status during the steady state in G6PD-deficient subjects. Acta Haematol 90:25-28, 1993.
26. Stevens DJ, Wanachiwanawin W, Mason PJ, Vulliamy TJ, Luzzatto L: G6PD Canton a common deficient variant in South East Asia caused by a 459 Arg -→ Leu mutation. Nucleic Acids Res 18:7190, 1990.