The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Common Severe Infections in Chronic Granulomatous Disease
Open accessAbstract
BACKGROUND: Chronic granulomatous disease (CGD) is due to defective nicotinamide adenine dinucleotide phosphate oxidase activity and characterized by recurrent infections with a limited spectrum of bacteria and fungi as well as inflammatory complications. To understand the impact of common severe infections in CGD, we examined the records of 268 patients followed at a single center over 4 decades. METHODS: All patients had confirmed diagnoses of CGD, and genotype was determined where possible. Medical records were excerpted into a standard format. Microbiologic analyses were restricted to Staphylococcus, Burkholderia, Serratia, Nocardia, and Aspergillus. RESULTS: Aspergillus incidence was estimated at 2.6 cases per 100 patient-years; Burkholderia, 1.06 per 100 patient-years; Nocardia, 0.81 per 100 patient-years; Serratia, 0.98 per 100 patient-years, and severe Staphylococcus infection, 1.44 per 100 patient-years. Lung infection occurred in 87% of patients, whereas liver abscess occurred in 32%. Aspergillus incidence was 55% in the lower superoxide-producing quartiles (quartiles 1 and 2) but only 41% in the higher quartiles (rate ratio, <0.0001). Aspergillus and Serratia were somewhat more common in lower superoxide producing gp91phox deficiency. The median age at death has increased from 15.53 years before 1990 to 28.12 years in the last decade. Fungal infection carried a higher risk of mortality than bacterial infection and was the most common cause of death (55%). Gastrointestinal complications were not associated with either infection or mortality. CONCLUSIONS: Fungal infections remain a major determinant of survival in CGD. X-linked patients generally had more severe disease, and this was generally in those with lower residual superoxide production. Survival in CGD has increased over the years, but infections are still major causes of morbidity and mortality.
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De Pauw, B., Walsh, T. J., Donnelly, J. P., Stevens, D. A., Edwards, J. E., Calandra, T., Pappas, P. G., Maertens, J., Lortholary, O., Kauffman, C. A., et al. (2008) · Clinical Infectious Diseases · doi:10.1086/588660 · Cited by 4,917
Residual NADPH Oxidase and Survival in Chronic Granulomatous Disease
Kuhns, D. B., Alvord, W. G., Heller, T., Feld, J. J., Pike, K. M., Marciano, B. E., Uzel, G., DeRavin, S. S., Priel, D. A. L., Soule, B. P., et al. (2010) · New England Journal of Medicine · doi:10.1056/nejmoa1007097 · Cited by 568
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Cited by
Superoxide Anion Chemistry—Its Role at the Core of the Innate Immunity
Andrés, C. M. C., Pérez de la Lastra, J. M., Andrés Juan, C., Plou, F. J., & Pérez-Lebeña, E. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24031841 · Cited by 342
NADPH oxidase activation in neutrophils: Role of the phosphorylation of its subunits
Belambri, S. A., Rolas, L., Raad, H., Hurtado‐Nedelec, M., Dang, P. M., & El‐Benna, J. (2018) · European Journal of Clinical Investigation · doi:10.1111/eci.12951 · Cited by 265
Nocardia Infection in Solid Organ Transplant Recipients: A Multicenter European Case-control Study
Coussement, J., for the European Study Group for Nocardia in Solid Organ Transplantation, Lebeaux, D., for the European Study Group for Nocardia in Solid Organ Transplantation, van Delden, C., for the European Study Group for Nocardia in Solid Organ Transplantation, Guillot, H., for the European Study Group for Nocardia in Solid Organ Transplantation, Freund, R., for the European Study Group for Nocardia in Solid Organ Transplantation, et al. (2016) · Clinical Infectious Diseases · doi:10.1093/cid/ciw241 · Cited by 264
Roos, D. (2016) · British Medical Bulletin · doi:10.1093/bmb/ldw009 · Cited by 212
Chronic Granulomatous Disease: a Comprehensive Review
Yu, H.-H., Yang, Y.-H., & Chiang, B.-L. (2021) · Clinical Reviews in Allergy & Immunology · doi:10.1007/s12016-020-08800-x · Cited by 197
Metadata
- Authors
- Marciano, B. E., Spalding, C., Fitzgerald, A., Mann, D., Brown, T., Osgood, S., Yockey, L., Darnell, D. N., Barnhart, L., Daub, J., Boris, L., Rump, A. P., Anderson, V. L., Haney, C., Kuhns, D. B., Rosenzweig, S. D., Kelly, C., Zelazny, A., Mason, T., DeRavin, S. S., Kang, E., Gallin, J. I., Malech, H. L., Olivier, K. N., Uzel, G., Freeman, A. F., Heller, T., Zerbe, C. S., & Holland, S. M.
- Venue
- Clinical Infectious Diseases
- Publisher
- Oxford University Press (OUP)
- Published
- 2014-12-23
- Volume
- 60
- Issue
- 8
- Pages
- 1176-1183
- ISSN
- 1058-4838 (ISSN-L)
- 1537-6591
- OpenAlex
- W2061652403
- Cited by
- 423
- References
- 2
- FWCI
- 9.98
- Type
- journal article
- Language
- en
- Open access
- green
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- Marciano, B. E., Spalding, C., Fitzgerald, A., Mann, D., Brown, T., Osgood, S., Yockey, L., Darnell, D. N., Barnhart, L., Daub, J., Boris, L., Rump, A. P., Anderson, V. L., Haney, C., Kuhns, D. B., Rosenzweig, S. D., Kelly, C., Zelazny, A., Mason, T., . . . Holland, S. M. (2015). Common Severe Infections in Chronic Granulomatous Disease. Clinical Infectious Diseases. https://doi.org/10.1093/cid/ciu1154
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