Journals of Gerontology Series A: Biological Sciences and Medical Sciences Large Type Edition
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The Journals of Gerontology Series A: Biological Sciences and Medical Sciences 61:1086-1089 (2006)
© 2006 The Gerontological Society of America

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Glucose-6-Phosphate Dehydrogenase Deficiency in Female Octogenarians, Nanogenarians, and Centenarians

Wing-Yan Au, Veronica Lam, Annie Pang, Wing-Man Lee, Jess L. C. Chan, You-Qiang Song, Edmond S. Ma and Yok-Lam Kwong

Departments of 1 Medicine, 2 Biochemistry, and 3 Pathology, and 4 Genome Research Center, University of Hong Kong.

Address correspondence to Yok Lam Kwong, MD, Department of Medicine, Professorial Block, Queen Mary Hospital, Pokfulam Road, Hong Kong. E-mail: ylkwong{at}hkucc.hku.hk

Abstract

Background. Age-related skewing of X-chromosome inactivation leading to glucose-6-phosphate dehydrogenase (G6PD) deficiency in elderly women in a population with prevalent G6PD gene mutations was investigated.

Methods. G6PD activity was measured biochemically. G6PD mutations were detected by polymerase chain reaction (PCR) and allele-specific extension, and analyzed by matrix-assisted laser desorption ionization–time of flight (MALDI-TOF) mass spectrometry and Sequenom MassARRAY. X-chromosome inactivation was quantified by semiquantitative PCR for the HUMARA gene, before and after HpaII digestion.

Results. In 173 women (median age: 90 years; range, 80–107 years), 18 heterozygotes for G6PD mutations were identified. Three heterozygotes were G6PD deficient, owing to skewed X-chromosome inactivation affecting the wild-type allele. Fifteen heterozygotes, with skewing apparently affecting the mutant alleles, had normal but significantly lower G6PD levels. At 1.73%, G6PD deficiency was significantly more frequent than expected from population screening at birth.

Conclusion. Due to skewed X-chromosome inactivation, elderly women in populations with prevalent G6PD mutations are at risk of G6PD deficiency.






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