Evaluation of glucose-6-phosphate dehydrogenase activity in two different ethnic groups using a kit employing the haemoglobin normalization procedure
Correct evaluation of Glucose-6-Phosphate Dehydrogenase (G-6-PD) activity of two ethnic groups using a fully quantitative kit with a simultaneous Hemoglobin Normalization (Hb Normalization) procedure. Two groups of mothers and their healthy full term newborns of Greek ( n = 1.166) and Albanian ( n =...
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| Published in | Clinical biochemistry Vol. 36; no. 5; pp. 393 - 395 |
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| Main Authors | , , , |
| Format | Journal Article |
| Language | English |
| Published |
United States
Elsevier Inc
01.07.2003
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| Subjects | |
| Online Access | Get full text |
| ISSN | 0009-9120 1873-2933 |
| DOI | 10.1016/S0009-9120(03)00034-1 |
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| Abstract | Correct evaluation of Glucose-6-Phosphate Dehydrogenase (G-6-PD) activity of two ethnic groups using a fully quantitative kit with a simultaneous Hemoglobin Normalization (Hb Normalization) procedure.
Two groups of mothers and their healthy full term newborns of Greek (
n = 1.166) and Albanian (
n = 818) origin were tested for their G-6-PD activity employing a direct normalization protocol.
Greek mothers and newborns showed a higher prevalence for G-6-PD deficiency as compared to those of Albanian origin. Males of G-6-PD deficient mothers confirmed the efficacy of the method.
A fully quantitative G-6-PD kit employing Hb Normalization is essential for the correct classification of G-6-PD activity, both in male and female subjects. |
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| AbstractList | Correct evaluation of Glucose-6-Phosphate Dehydrogenase (G-6-PD) activity of two ethnic groups using a fully quantitative kit with a simultaneous Hemoglobin Normalization (Hb Normalization) procedure.
Two groups of mothers and their healthy full term newborns of Greek (n = 1.166) and Albanian (n = 818) origin were tested for their G-6-PD activity employing a direct normalization protocol.
Greek mothers and newborns showed a higher prevalence for G-6-PD deficiency as compared to those of Albanian origin. Males of G-6-PD deficient mothers confirmed the efficacy of the method.
A fully quantitative G-6-PD kit employing Hb Normalization is essential for the correct classification of G-6-PD activity, both in male and female subjects. Correct evaluation of Glucose-6-Phosphate Dehydrogenase (G-6-PD) activity of two ethnic groups using a fully quantitative kit with a simultaneous Hemoglobin Normalization (Hb Normalization) procedure.AIMCorrect evaluation of Glucose-6-Phosphate Dehydrogenase (G-6-PD) activity of two ethnic groups using a fully quantitative kit with a simultaneous Hemoglobin Normalization (Hb Normalization) procedure.Two groups of mothers and their healthy full term newborns of Greek (n = 1.166) and Albanian (n = 818) origin were tested for their G-6-PD activity employing a direct normalization protocol.DESIGN AND METHODSTwo groups of mothers and their healthy full term newborns of Greek (n = 1.166) and Albanian (n = 818) origin were tested for their G-6-PD activity employing a direct normalization protocol.Greek mothers and newborns showed a higher prevalence for G-6-PD deficiency as compared to those of Albanian origin. Males of G-6-PD deficient mothers confirmed the efficacy of the method.RESULTSGreek mothers and newborns showed a higher prevalence for G-6-PD deficiency as compared to those of Albanian origin. Males of G-6-PD deficient mothers confirmed the efficacy of the method.A fully quantitative G-6-PD kit employing Hb Normalization is essential for the correct classification of G-6-PD activity, both in male and female subjects.CONCLUSIONA fully quantitative G-6-PD kit employing Hb Normalization is essential for the correct classification of G-6-PD activity, both in male and female subjects. Correct evaluation of Glucose-6-Phosphate Dehydrogenase (G-6-PD) activity of two ethnic groups using a fully quantitative kit with a simultaneous Hemoglobin Normalization (Hb Normalization) procedure. Two groups of mothers and their healthy full term newborns of Greek ( n = 1.166) and Albanian ( n = 818) origin were tested for their G-6-PD activity employing a direct normalization protocol. Greek mothers and newborns showed a higher prevalence for G-6-PD deficiency as compared to those of Albanian origin. Males of G-6-PD deficient mothers confirmed the efficacy of the method. A fully quantitative G-6-PD kit employing Hb Normalization is essential for the correct classification of G-6-PD activity, both in male and female subjects. |
| Author | Reclos, George J. Vlachos, George Gavrili, Stavroula Schulpis, Kleopatra H. |
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| Cites_doi | 10.1182/blood.V32.5.816.816 10.1016/S0022-3476(05)80747-4 10.1159/000204709 10.1542/peds.104.1.68 10.1203/00006450-196909000-00008 10.1136/jms.7.1.46 10.1067/mpd.2001.115312 |
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| Keywords | Glucose-6-phosphate dehydrogenase Profound G-6-PD deficiency G-6-PD Partial G-6-PD deficiency Hemoglobin normalization |
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| References_xml | – volume: 119 start-page: 293 year: 1991 end-page: 299 ident: BIB2 article-title: Screening for glucose-6-phosphate deficiency as a preventive measure publication-title: J Paediatr – reference: Sampaio, C., Reclos, GJ., Gallotti Povoa, Mack Fadden, N., Pass, K. Haemoglobin normalization leads to correct classification of samples derived from wrong blood spots. 5 – reference: Bartsocas, Ch., Red cell enzymopathies and screening. Proceedings of the EEC Workshop, London March 1983. In Benson PE Ed. Screening and management of potentially treatable genetic disorders. London, MTP Press,1983, pp. 480-4 – volume: 27 start-page: 137 year: 1990 end-page: 164 ident: BIB6 article-title: The genetics of glucose-6-phosphate dehydrogenase deficiency publication-title: Semin Hematol – volume: 32 start-page: 826 year: 1968 end-page: 830 ident: BIB10 article-title: Special modification of the fluorescent screening method for G6PD deficiency publication-title: Blood – volume: 87 start-page: 29 year: 1999 end-page: 31 ident: BIB3 article-title: Marked decline of favism after neonatal glucose-6-phosphate dehydrogenase screening and health education publication-title: Acta Haematol – reference: Meeting of the International Society for Neonatal Screening. Genova, Italy, June 26–29, 2002 – volume: 104 start-page: 68 year: 1999 end-page: 74 ident: BIB7 article-title: Neonatal hyperbilirubinemia in glucose-6-phosphate dehydrogenase-deficient heterozygotes publication-title: Pediatrics – volume: 3 start-page: 448 year: 1969 end-page: 458 ident: BIB1 article-title: Incidence and mechanism of neonatal jaundice related to glucose-6-phosphate dehydrogenase deficiency publication-title: Pediatr Res – volume: 7 start-page: 46 year: 2000 end-page: 51 ident: BIB5 article-title: Glucose-6-phosphate dehydrogenase deficiency neonatal screening publication-title: J Med Screening – volume: 139 start-page: 137 year: 2001 end-page: 140 ident: BIB8 article-title: Acute haemolysis hyperbilirubinemia in glucose-6-phosphate dehydrogenase deficient heterozygotes publication-title: J Paediatr – volume: 32 start-page: 826 year: 1968 ident: 10.1016/S0009-9120(03)00034-1_BIB10 article-title: Special modification of the fluorescent screening method for G6PD deficiency publication-title: Blood doi: 10.1182/blood.V32.5.816.816 – volume: 119 start-page: 293 year: 1991 ident: 10.1016/S0009-9120(03)00034-1_BIB2 article-title: Screening for glucose-6-phosphate deficiency as a preventive measure publication-title: J Paediatr doi: 10.1016/S0022-3476(05)80747-4 – volume: 87 start-page: 29 year: 1999 ident: 10.1016/S0009-9120(03)00034-1_BIB3 article-title: Marked decline of favism after neonatal glucose-6-phosphate dehydrogenase screening and health education publication-title: Acta Haematol doi: 10.1159/000204709 – ident: 10.1016/S0009-9120(03)00034-1_BIB9 – volume: 104 start-page: 68 year: 1999 ident: 10.1016/S0009-9120(03)00034-1_BIB7 article-title: Neonatal hyperbilirubinemia in glucose-6-phosphate dehydrogenase-deficient heterozygotes publication-title: Pediatrics doi: 10.1542/peds.104.1.68 – volume: 3 start-page: 448 year: 1969 ident: 10.1016/S0009-9120(03)00034-1_BIB1 article-title: Incidence and mechanism of neonatal jaundice related to glucose-6-phosphate dehydrogenase deficiency publication-title: Pediatr Res doi: 10.1203/00006450-196909000-00008 – volume: 7 start-page: 46 year: 2000 ident: 10.1016/S0009-9120(03)00034-1_BIB5 article-title: Glucose-6-phosphate dehydrogenase deficiency neonatal screening publication-title: J Med Screening doi: 10.1136/jms.7.1.46 – volume: 27 start-page: 137 year: 1990 ident: 10.1016/S0009-9120(03)00034-1_BIB6 article-title: The genetics of glucose-6-phosphate dehydrogenase deficiency publication-title: Semin Hematol – ident: 10.1016/S0009-9120(03)00034-1_BIB4 – volume: 139 start-page: 137 year: 2001 ident: 10.1016/S0009-9120(03)00034-1_BIB8 article-title: Acute haemolysis hyperbilirubinemia in glucose-6-phosphate dehydrogenase deficient heterozygotes publication-title: J Paediatr doi: 10.1067/mpd.2001.115312 |
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| SubjectTerms | Albania - ethnology Female G-6-PD Glucose-6-phosphate dehydrogenase Glucosephosphate Dehydrogenase - blood Glucosephosphate Dehydrogenase Deficiency - blood Glucosephosphate Dehydrogenase Deficiency - ethnology Greece Hemoglobin normalization Hemoglobins - analysis Humans Infant, Newborn Male Partial G-6-PD deficiency Profound G-6-PD deficiency |
| Title | Evaluation of glucose-6-phosphate dehydrogenase activity in two different ethnic groups using a kit employing the haemoglobin normalization procedure |
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