Abstract
Chronic granulomatous disease is a rare immunodeficiency due to defects in the phagocyte NADPH oxidase. The X-linked form (gp91 (phox) deficiency) accounts for about 70 % of cases; autosomal recessive p47 (phox) deficiency accounts for about 25 % of cases. We identified a 10 % incidence of diabetes in p47 (phox) deficient CGD, but none in X-linked CGD. Renal and cardiovascular diseases were also higher in p47 (phox) deficiency. p47 (phox) deficient CGD has non-infectious morbidities distinct from those in X-linked CGD.
Publication types
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Research Support, N.I.H., Intramural
MeSH terms
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Adolescent
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Adult
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Cardiovascular Diseases / epidemiology*
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Cardiovascular Diseases / genetics
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Comorbidity
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Diabetes Mellitus / epidemiology*
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Diabetes Mellitus / genetics
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Female
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Granulomatous Disease, Chronic / epidemiology*
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Granulomatous Disease, Chronic / genetics
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Humans
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Male
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Membrane Glycoproteins / genetics
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Middle Aged
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NADPH Oxidase 2
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NADPH Oxidases / genetics*
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Phagocytes / immunology
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Phagocytes / metabolism*
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Phagocytes / pathology
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Renal Insufficiency, Chronic / epidemiology*
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Renal Insufficiency, Chronic / genetics
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Young Adult
Substances
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Membrane Glycoproteins
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CYBB protein, human
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NADPH Oxidase 2
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NADPH Oxidases
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neutrophil cytosolic factor 1