The DOI matches its Crossref record; 30 of the 30 references it cites were found in a registry or an index.
Bone Aluminum and Histomorphometric Features of Renal Osteodystrophy*
Abstract
To evaluate the relationship between aluminum and the characteristics of bone disease in uremia, bone aluminum content and quantitative histomorphometric analysis of bone were evaluated in bone biopsies from 59 uremic patients undergoing maintenance hemodialysis. Biopsies were classified as showing 1) pure osteomalacia (OM) in 23 cases, 2) osteitis fibrosa (OF) in 13, 3) mixed in 7, and 4) mild lesions in 16. There were no significant differences in levels of serum calcium or alkaline phosphatase between the groups, but serum phosphorus levels were slightly higher in those with OF. Serum immunoreactive parathyroid hormone levels were greater in the patients with OF and mixed lesions than in patients with OM or mild lesions (P less than 0.01). Bone aluminum exceeded normal in all groups (P less than 0.01), with values of 175 +/- 18 mg/kg dry wt in OM patients, 46 +/- 7 of OF patients, 81 +/- 29 in mixed subjects, and 67 +/- 7 in patients with mild lesions. Bone aluminum was significantly higher in the OM patients than in any other group (P less than 0.01); also, bone aluminum correlated with the quantitative measure of unmineralized osteoid in OM (r = 0.67; P less than 0.001); no correlations existed for the other groups. There were inverse correlations between bone aluminum and the serum immunoreactive parathyroid hormone (r = -0.35; P less than 0.01) and resorbing surface on biopsy (r = -0.44; P less than 0.001). Bone aluminum correlated with the duration of hemodialysis in patients with OF with mixed and mild lesions (r = 0.49); no relation was seen in OM patients, and bone aluminum was higher for the duration of dialysis, suggesting that aluminum may accumulate more rapidly in OM subjects. These findings are consistent with but do not prove the hypothesis that aluminum plays a pathogenic role in dialysis osteomalacia; the mechanism by which aluminum accumulates remains unknown.
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Citations
Cites
A Multiple Comparison Procedure for Comparing Several Treatments with a Control
Dunnett, C. W. (1955) · Journal of the American Statistical Association · doi:10.1080/01621459.1955.10501294 · Cited by 6,094
The Dialysis Encephalopathy Syndrome: Possible Aluminum Intoxication
Alfrey, A. C., LeGendre, G. R., & Kaehny, W. D. (1976) · New England Journal of Medicine · doi:10.1056/nejm197601222940402 · Cited by 1,621
Self-citationWard, M. K., Ellis, H. A., Feest, T. G., Parkinson, I. S., Kerr, D. N. S., Herrington, J., & Goode, G. L. (1978) · The Lancet · doi:10.1016/s0140-6736(78)90191-5 · Cited by 439
Gastrointestinal Absorption of Aluminum from Aluminum-Containing Antacids
Kaehny, W. D., Hegg, A. P., & Alfrey, A. C. (1977) · New England Journal of Medicine · doi:10.1056/nejm197706162962407 · Cited by 398
Self-citationFRACTURING DIALYSIS OSTEODYSTROPHY AND DIALYSIS ENCEPHALOPATHY
Parkinson, I. S., Feest, T. G., Kerr, D. N. S., Ward, M. K., & Fawcett, R. W. P. (1979) · The Lancet · doi:10.1016/s0140-6736(79)90883-3 · Cited by 373
Metabolism and toxicity of aluminum in renal failure
Alfrey, A. C., Hegg, A., & Craswell, P. (1980) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/33.7.1509 · Cited by 278
Self-citationEllis, H. A., McCarthy, J. H., & Herrington, J. (1979) · Journal of Clinical Pathology · doi:10.1136/jcp.32.8.832 · Cited by 266
HYPERALUMINqMIA FROM ALUMINIUM RESINS IN RENAL FAILURE
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Platts, M. M., Goode, G. C., & Hislop, J. S. (1977) · BMJ · doi:10.1136/bmj.2.6088.657 · Cited by 239
Hemodialysis encephalopathy with osteomalacic fractures and muscle weakness
Pierides, A. M., Edwards Jr., W. G., Cullum Jr, U. X., McCall, J. T., & Ellis, H. A. (1980) · Kidney International · doi:10.1038/ki.1980.117 · Cited by 231
Cited by
Renal bone disease 1990: An unmet challenge for the nephrologist
Malluche, H., & Faugere, M.-C. (1990) · Kidney International · doi:10.1038/ki.1990.187 · Cited by 362
Ott, S. M., Maloney, N. A., Coburn, J. W., Alfrey, A. C., & Sherrard, D. J. (1982) · New England Journal of Medicine · doi:10.1056/nejm198209163071202 · Cited by 353
Self-citationSlatopolsky, E. A., Burke, S. K., & Dillon, M. A. (1999) · Kidney International · doi:10.1046/j.1523-1755.1999.00240.x · Cited by 302
Aplastic osteodystrophy without aluminum: The role of “suppressed” parathyroid function
Hercz, G., Pei, Y., Greenwood, C., Manuel, A., Saiphoo, C., Goodman, W. G., Segre, G. V., Fenton, S., & Sherrard, D. J. (1993) · Kidney International · doi:10.1038/ki.1993.323 · Cited by 281
Self-citationMalluche, H. H., Smith, A. J., Abreo, K., & Faugere, M.-C. (1984) · New England Journal of Medicine · doi:10.1056/nejm198407193110302 · Cited by 199
Metadata
- Authors
- HODSMAN, A. B., SHERRARD, D. J., ALFREY, A. C., OTT, S., BRICKMAN, A. S., MILLER, N. L., MALONEY, N. A., & COBURN, J. W.
- Venue
- The Journal of Clinical Endocrinology & Metabolism
- Publisher
- The Endocrine Society
- Published
- 1982-03
- Volume
- 54
- Issue
- 3
- Pages
- 539-546
- ISSN
- 0021-972X (ISSN-L)
- 1945-7197
- OpenAlex
- W2055398335
- Cited by
- 272
- References
- 30
- FWCI
- 25.96
- Type
- journal article
- Language
- en
- Open access
- closed
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