Open-access Bone aluminum accumulation in the current era

Abstracts

In the last few years, evidence from the Brazilian Registry of Bone Biopsy (REBRABO) has pointed out a high incidence of aluminum (Al) accumulation in the bones of patients with CKD under dialysis. This surprising finding does not appear to be merely a passive metal accumulation, as prospective data from REBRABO suggest that the presence of Al in bone may be independently associated with major adverse cardiovascular events. This information contrasts with the perception of epidemiologic control of this condition around the world. In this opinion paper, we discussed why the diagnosis of Al accumulation in bone is not reported in other parts of the world. We also discuss a range of possibilities to understand why bone Al accumulation still occurs, not as a classical syndrome with systemic signs of intoxication, as occurred it has in the past.

Keywords: Chronic Kidney Disease-Mineral and Bone Disorder; Aluminum; Renal Insufficiency; Chronic; Treatment Outcome


Nos últimos anos, evidências do Registro Brasileiro de Biópsia óssea (REBRABO) apontaram uma alta incidência de intoxicação por alumínio (Al) no tecido ósseo de pacientes com DRC em diálise. Essa surpreendente informação parece representar não apenas um acúmulo passivo deste metal, visto que dados prospectivos do REBRABO sugerem que a presença de Al no tecido ósseo pode estar independentemente relacionada a eventos cardiovasculares adversos maiores. Essas informações contrastam com a percepção mundial do controle epidemiológico dessa condição. Neste artigo de opinião, discutimos por que o diagnóstico de acúmulo ósseo de Al não é relatado em outras partes do mundo, e também discutimos uma gama de possibilidades para entender por que nós acreditamos que o acúmulo de Al no tecido ósseo ainda ocorre, não como se apresentava no passado, ou seja, como uma síndrome com sinais e sintomas sistêmicos de intoxicação.

Palavras-chave Distúrbio Mineral e Ósseo na Doença Renal Crônica; Alumínio; Insuficiência Renal Crônica; Resultado do Tratamento


Introduction

About fifty years ago, nephrologists faced a devastating clinical problem: patients under hemodialysis treatment who presented dementia, anemia, and bone fractures due to mineralization disorders. The cause of this syndrome was the excess of aluminum (Al) in the blood and different organs, including the skeleton1. Since then, several measures have been taken to protect patients with chronic kidney disease (CKD) from Al exposure. Strategies to remove Al in the water used for hemodialysis, avoidance of Al-based phosphate binders, and drugs to increase hemodialysis clearance of Al resulted in the epidemiologic control of this condition. This control was confirmed in clinical settings, and over time, different studies documented low (apparently, safe) serum Al levels in these patients1,2,3,4.

However, in the last few years, contrasting evidence from the Brazilian Registry of Bone Biopsy (REBRABO) has pointed out a high incidence of Al accumulation in the bones of patients with CKD5,6. Clinical outcome data from this registry suggest that the presence of this metal in bone is not only an isolated histological finding. In a cohort of 275 patients with CKD followed by 3.4 years, the diagnosis of bone Al accumulation was independently associated with major adverse cardiovascular events (MACE) [HR = 3.129 (CI: 1.439–6.804; p = 0.004)]7.

These surprising data should make us reflect on this subject. Do these findings reflect a local problem? Do other populations in other countries also suffer from a high incidence of bone Al accumulation and may be exposed to an additional risk factor for cardiovascular complications?

Our opinion is that bone Al accumulation still occurs, but not as a classic syndrome with systemic signs of intoxication, as it has in the past. Instead, prolonged and low exposure to Al sources may result in bone Al accumulation and may be linked to adverse clinical consequences. In the next sessions, we present arguments to support our opinion.

Why is it Plausible that Prolonged Low-Intensity Exposures to al Sources Still Occur?

The increasing incidence and prevalence of CKD places a burden on healthcare systems, particularly in terms of access to dialysis treatment. This sustained and progressive pressure in healthcare systems leads to heterogeneity in the quality of care provided and can affect the standards of water used for hemodialysis8,9,10,11,12,13.

Many situations have risks for exposure to Al sources, such as limited legal regulation of dialysis treatment12, insufficient quality control related to the presence of Al in water used for safe hemodialysis, either because of infrequency of measurements or because of inadequate cutoff levels, non-negligible amounts of Al in raw materials used in oral and intravenous drugs14, and Al absorption by the digestive tract15. Meira et al. published a thorough discussion of possible sources of Al contamination in patients in dialysis16. Figure 1 shows possible sources of Al exposure in patients under dialysis.

Figure 1
Patients with chronic kidney disease under dialysis can be exposed to many aluminum sources: water used in hemodialysis, pots and cans made of aluminum, and raw materials for oral and intravenous drugs. The current quality control for water used in hemodialysis can be inadequate in terms of frequency and maximum allowable Al limit to avoid accumulation.

Why is Bone al Accumulation not Reported in other Countries?

First, it is important to highlight that Brazilian public and private dialysis facilities have generally adopted the international guidelines for the prevention of Al intoxication17. A federal law guarantees this standard, and there is a governmental agency (Agência Nacional de Vigilância Sanitária) in charge of enforcing the law and carrying out preventive surveillance18. The reports related to Al accumulation in patients with CKD are not limited to Brazil. Other groups from China have also found Al accumulation and an association with uremic pruritus and increased mortality in hemodialysis patients19,20.

We propose three main possibilities to explain the actual lack of Al detection in patients with CKD under dialysis in other countries: (1) Al serum levels may not reflect Al deposition in tissue; as a cation, Al measurement may be affected by other cations such as iron and by eventual Al binding to transferrin21; (2) periodic measurements of serum Al levels may not reflect low and chronic exposures to Al sources22; (3) currently, bone Al intoxication (as a rare diagnosis) is mainly diagnosed by measurements of serum Al levels in cohorts of patients with CKD, and not by bone tissue analysis2333. Table 1 summarizes the main studies on renal osteodystrophy in recent decades and its relationship with the active search for Al intoxication on bone biopsies through the gold standard technique (solochrome azurine staining). Of note, most studies did not perform (or did not report) this technique for the diagnosis of bone Al accumulation, despite performing bone biopsy and histologic analysis.

Table 1
Summary of studies related to incidence of bone al accumulation with study period, country, and ethnicity. Most of the studies did not provide information on this diagnosis (highlighted in black bold: na)

As most studies did not provide information on the incidence of bone Al accumulation, in our opinion, the only way to know the true global prevalence of this condition in the current era is to systematically perform staining with solochrome azurine associated with staining with Pearls for iron detection in all bone samples from a representative sample of patients with CKD.

Until new evidence becomes available, we believe that nephrologists should consider bone Al accumulation as a possible diagnosis, even in asymptomatic patients with CKD under dialysis. An active search for Al detection in all bone biopsy samples from patients with CKD is advised. We must keep in mind that there is an established treatment for Al accumulation in bone34.

The standards for water quality in hemodialysis should have a “zero” Al limit as an ideal target. In addition, we propose a list of research gaps and key directions for research on this subject (Chart 1).

Chart 1
Proposed list information gaps and key directions for future research

Conclusion

Our opinion is that bone Al accumulation should be considered as a potential frequent diagnosis, even nowadays. We urge other colleagues to actively search for this diagnosis in patients with CKD under dialysis in other geographic regions, including those who are presumably free of Al accumulation. Only then can we determine whether this is a restricted problem or a problem that chronically affects a larger population and with negative impact on clinical outcomes.

Meanwhile, efforts to improve the quality of water used for hemodialysis would be desirable, at least at local level, including reducing the allowed concentration of this metal in water to levels close to zero and increasing the frequency of measurements.

Acknowledgments

A. L. Mendes, for Figure 1 first draft; the authors acknowledge the Brazilian Society of Nephrology (BSN) to the support for the Brazilian Registry of Bone Biopsy – REBRABO.

References

  • 1. Dunea G. Dialysis dementia: an epidemic that came and went. ASAIO J. 2001;47(3):192–4. doi: http://dx.doi.org/10.1097/00002480-200105000-00002. PubMed PMID: 11374754.
    » https://doi.org/10.1097/00002480-200105000-00002
  • 2. Fernandez-Martın JL, Canteros A, Serrano M, González-Carcedo A, Díaz-Corte C, Cannata Andía JB. Prevention of aluminium exposure through dialysis fluids. Analysis of changes in the last 8 years. Nephrol Dial Transplant. 1998;13(Suppl. 3):78–81. doi: http://dx.doi.org/10.1093/ndt/13.suppl_3.78. PubMed PMID: 9568827.
    » https://doi.org/10.1093/ndt/13.suppl_3.78
  • 3. Smith GD, Winney RJ, McLean A, Robson JS. Aluminium-related osteomalacia: response to reverse osmosis water treatment. Kidney Int. 1987;32(1):96–101. doi: http://dx.doi.org/10.1038/ki.1987.177. PubMed PMID: 3626303.
    » https://doi.org/10.1038/ki.1987.177
  • 4. Malluche HH. Aluminum and bone disease in chronic renal failure. Nephrol Dial Transplant. 2002;17(Suppl 2):21–4. doi: http://dx.doi.org/10.1093/ndt/17.suppl_2.21. PubMed PMID: 11904354.
    » https://doi.org/10.1093/ndt/17.suppl_2.21
  • 5. Carbonara CEM, Reis LMD, Quadros KRDS, Roza NAV, Sano R, Carvalho AB, et al. Renal osteodystrophy and clinical outcomes: data from the Brazilian Registry of Bone Biopsies—REBRABO. J Bras Nefrol. 2020;42(2):138–46. doi: http://dx.doi.org/10.1590/2175-8239-jbn-2019-0045. PubMed PMID: 32756862.
    » https://doi.org/10.1590/2175-8239-jbn-2019-0045
  • 6. Carbonara CEM, Roza NAV, Reis LMD, Carvalho AB, Jorgetti V, Oliveira RB. Overview of renal osteodystrophy in Brazil: a cross-sectional study. Braz J Nephrol. 2023;45(2):257–64. doi: http://dx.doi.org/10.1590/2175-8239-jbn-2022-0146pt. PubMed PMID: 37158484.
    » https://doi.org/10.1590/2175-8239-jbn-2022-0146pt
  • 7. Carbonara CEM, Roza NAV, Quadros KRS, França RA, Esteves ABA, Pavan CR, et al. Effect of aluminum accumulation on bone and cardiovascular risk in the current era. PLoS One. 2023;18(4):e0284123. doi: http://dx.doi.org/10.1371/journal.pone.0284123. PubMed PMID: 37079520.
    » https://doi.org/10.1371/journal.pone.0284123
  • 8. Himmelfarb J, Vanholder R, Mehrotra R, Tonelli M. The current and future landscape of dialysis. Nat Rev Nephrol. 2020;16(10):573–85. doi: http://dx.doi.org/10.1038/s41581-020-0315-4. PubMed PMID: 32733095.
    » https://doi.org/10.1038/s41581-020-0315-4
  • 9. Remuzzi G, Mendis S, Tonelli M. The contribution of chronic kidney disease to the global burden of major noncommunicable diseases. Kidney Int. 2011;80(12):1258–70. doi: http://dx.doi.org/10.1038/ki.2011.368. PubMed PMID: 21993585.
    » https://doi.org/10.1038/ki.2011.368
  • 10. Garcia-Garcia G, Jha V, World Kidney Day Steering Committee. CKD in disadvantaged populations. Kidney Int. 2015;87(2):251–3. doi: http://dx.doi.org/10.1038/ki.2014.369. PubMed PMID: 25635713.
    » https://doi.org/10.1038/ki.2014.369
  • 11. Jha V, Wang AY, Wang H. The impact of CKD identification in large countries: the burden of illness. Nephrol Dial Transplant. 2012;27(Suppl 3):iii32–8. doi: http://dx.doi.org/10.1093/ndt/gfs113. PubMed PMID: 23115140.
    » https://doi.org/10.1093/ndt/gfs113
  • 12. Prasad N, Jha V. Hemodialysis in Asia. Kidney Dis. 2015;1(3):165–77. doi: http://dx.doi.org/10.1159/000441816. PubMed PMID: 27536677.
    » https://doi.org/10.1159/000441816
  • 13. Sola L, Levin NW, Johnson DW, Pecoits-Filho R, Aljubori HM, Chen Y, et al. Development of a framework for minimum and optimal safety and quality standards for hemodialysis and peritoneal dialysis. Kidney Int Suppl. 2020;10(1):e55–62. doi: http://dx.doi.org/10.1016/j.kisu.2019.11.009. PubMed PMID: 32149009.
    » https://doi.org/10.1016/j.kisu.2019.11.009
  • 14. Bohrer D, Bertagnolli DC, Oliveira SM, Nascimento PC, de Carvalho LM, Pomblum SG. Drugs as a hidden source of aluminium for chronic renal patients. Nephrol Dial Transplant. 2007;22(2):605–11. doi: http://dx.doi.org/10.1093/ndt/gfl569. PubMed PMID: 17035374.
    » https://doi.org/10.1093/ndt/gfl569
  • 15. Drueke TB. Intestinal absorption of aluminum in renal failure. Nephrol Dial Transplant. 2002;17(Suppl 2):13–6. doi: http://dx.doi.org/10.1093/ndt/17.suppl_2.13. PubMed PMID: 11904352.
    » https://doi.org/10.1093/ndt/17.suppl_2.13
  • 16. Meira RD, Carbonara CEM, Quadros KRDS, Santos CUD, Schincariol P, Pêssoa GS, et al. The enigma of aluminum deposition in bone tissue from a patient with chronic kidney disease: a case report. J Bras Nefrol. 2018;40(2):201–5. doi: http://dx.doi.org/10.1590/2175-8239-jbn-3882. PubMed PMID: 29927461.
    » https://doi.org/10.1590/2175-8239-jbn-3882
  • 17. National Kidney Foundation. K/DOQI clinical practice guidelines for bone metabolism and disease in chronic kidney disease. Am J Kidney Dis. 2003;42(4, Suppl 3):S1–201. PubMed PMID: 14520607.
  • 18. Brasil. Resolução da Diretoria Colegiada – RDC n° 11, de 13 de Março de 2014. Dispõe sobre os Requisitos de Boas Práticas de Funcionamento para os Serviços de Diálise e dá outras providências. Diário Oficial da União [Internet]; Brasília; 2014. [cited 2023 Dec 20]. Available from: https://bvsms.saude.gov.br/bvs/saudelegis/anvisa/2014/rdc0011_13_03_2014.pdf
    » https://bvsms.saude.gov.br/bvs/saudelegis/anvisa/2014/rdc0011_13_03_2014.pdf
  • 19. Hsu CW, Weng CH, Chan MJ, Lin-Tan DT, Yen TH, Huang WH. Association between serum aluminum level and uremic pruritus in hemodialysis patients. Sci Rep. 2018;8(1):17251. doi: http://dx.doi.org/10.1038/s41598-018-35217-6. PubMed PMID: 30467375.
    » https://doi.org/10.1038/s41598-018-35217-6
  • 20. Hsu CW, Weng CH, Lee CC, Lin-Tan DT, Chen KH, Yen TH, et al. Association of low serum aluminum level with mortality in hemodialysis patients. Ther Clin Risk Manag. 2016;12:1417–24. doi: http://dx.doi.org/10.2147/TCRM.S113829. PubMed PMID: 27695338.
    » https://doi.org/10.2147/TCRM.S113829
  • 21. El Hage Chahine J-M, Hémadi M, Ha-Duong NT. Uptake and release of metal ions by transferrin and interaction with receptor 1. Biochim Biophys Acta. 2012;1820(3):334–47. doi: http://dx.doi.org/10.1016/j.bbagen.2011.07.008. PubMed PMID: 21872645.
    » https://doi.org/10.1016/j.bbagen.2011.07.008
  • 22. Cannata-Andia JB. Reconsidering the importance of long-term low-level aluminum exposure in renal failure patients. Semin Dial. 2001;14(1):5–7. doi: http://dx.doi.org/10.1046/j.1525-139x.2001.00002.x. PubMed PMID: 11208028.
    » https://doi.org/10.1046/j.1525-139x.2001.00002.x
  • 23. Díaz López JB, Jorgetti V, Caorsi H, Ferreira A, Palma A, Menendez P, et al. Epidemiology of renal osteodystrophy in Iberoamerica. Nephrol Dial Transplant. 1998;13(Suppl 3):41–5. doi: http://dx.doi.org/10.1093/ndt/13.suppl_3.41. PubMed PMID: 9568819.
    » https://doi.org/10.1093/ndt/13.suppl_3.41
  • 24. Sprague SM, Bellorin-Font E, Jorgetti V, Carvalho AB, Malluche HH, Ferreira A, et al. Diagnostic accuracy of bone turnover markers and bone histology in patients with CKD treated by dialysis. Am J Kidney Dis. 2016;67(4):559–66. doi: http://dx.doi.org/10.1053/j.ajkd.2015.06.023. PubMed PMID: 26321176.
    » https://doi.org/10.1053/j.ajkd.2015.06.023
  • 25. Malluche HH, Mawad HW, Monier-Faugere MC. Renal osteodystrophy in the first decade of the new millennium: analysis of 630 bone biopsies in black and white patients. J Bone Miner Res. 2011;26(6):1368–76. doi: http://dx.doi.org/10.1002/jbmr.309. PubMed PMID: 21611975.
    » https://doi.org/10.1002/jbmr.309
  • 26. Moore C, Yee J, Malluche HH, Rao DS, Monier-Faugere MC, Adams E, et al. Relationship between bone histology and markers of bone and mineral metabolism in African-American hemodialysis patients. Clin J Am Soc Nephrol. 2009;4(9):1484–93. doi: http://dx.doi.org/10.2215/CJN.01770408. PubMed PMID: 19713297.
    » https://doi.org/10.2215/CJN.01770408
  • 27. Jørgensen HS, Ferreira AC, D’Haese P, Haarhaus M, Vervloet M, Lafage-Proust MH, et al. Bone histomorphometry for the diagnosis of renal osteodystrophy: a call for harmonization of reference. Kidney Int. 2022;102(2):431–4. doi: http://dx.doi.org/10.1016/j.kint.2022.04.030. PubMed PMID: 35643374.
    » https://doi.org/10.1016/j.kint.2022.04.030
  • 28. Salam S, Gallagher O, Hughes D, Khwaja A, Eastell R. The role of static bone histomorphometry in diagnosing renal osteodystrophy. Bone. 2021;142:115689. doi: http://dx.doi.org/10.1016/j.bone.2020.115689. PubMed PMID: 33065356.
    » https://doi.org/10.1016/j.bone.2020.115689
  • 29. Carbonara CEM, Barreto J, Roza NAV, Quadro KRS, Reis LM, Carvalho AB, et al. Renal osteodystrophy and clinical outcomes: a prospective cohort study. J Braz Nephrol. 2023;46(2):e20230119. doi: https://doi.org/10.1590/2175-8239-JBN-2023-0119en.
    » https://doi.org/10.1590/2175-8239-JBN-2023-0119en
  • 30. Gentry J, Webb J, Davenport D, Malluche HH. Serum phosphorus adds to value of serum parathyroid hormone for assessment of bone turnover in renal osteodystrophy. Clin Nephrol. 2016;86(7):9–17. doi: http://dx.doi.org/10.5414/CN108823. PubMed PMID: 27191663.
    » https://doi.org/10.5414/CN108823
  • 31. Lavigne F, Desbiens LC, Garneau G, Côté F, Mac-Way F. Iliac crest bone biopsy by interventional radiologists to improve access to bone biopsy in chronic kidney disease populations: technical note and a case series. J Nephrol. 2021;34(3):901–6. doi: http://dx.doi.org/10.1007/s40620-020-00798-x. PubMed PMID: 32656748.
    » https://doi.org/10.1007/s40620-020-00798-x
  • 32. Aaltonen L, Koivuviita N, Seppänen M, Burton IS, Kröger H, Löyttyniemi E, et al. Bone histomorphometry and 18F-sodium fluoride positron emission tomography imaging: comparison between only bone turnover-based and unified tmv-based classification of renal osteodystrophy. Calcif Tissue Int. 2021;109(6):605–14. doi: http://dx.doi.org/10.1007/s00223-021-00874-9. PubMed PMID: 34137924.
    » https://doi.org/10.1007/s00223-021-00874-9
  • 33. Novel-Catin E, Pelletier S, Fouque D, Roux JP, Chapurlat R, D’Haese P, et al. Quantitative histomorphometric analysis of halved iliac crest bone biopsies yield comparable ROD diagnosis as full 7.5mm wide samples. Bone. 2020;138:115460. doi: http://dx.doi.org/10.1016/j.bone.2020.115460. PubMed PMID: 32485361.
    » https://doi.org/10.1016/j.bone.2020.115460
  • 34. Oliveira RB, Barreto FC, Nunes LA, Custódio MR. Aluminum intoxication in chronic kidney disease. J Bras Nefrol. 2021;43(4, Suppl 1):660–4. doi: http://dx.doi.org/10.1590/2175-8239-jbn-2021-s110. PubMed PMID: 34910802.
    » https://doi.org/10.1590/2175-8239-jbn-2021-s110

Publication Dates

  • Publication in this collection
    29 Apr 2024
  • Date of issue
    Jul-Sep 2024

History

  • Received
    05 Feb 2024
  • Accepted
    22 Mar 2024
location_on
Sociedade Brasileira de Nefrologia Rua Machado Bittencourt, 205 - 5ºandar - conj. 53 - Vila Clementino - CEP:04044-000 - São Paulo SP, Telefones: (11) 5579-1242/5579-6937, Fax (11) 5573-6000 - São Paulo - SP - Brazil
E-mail: bjnephrology@gmail.com
rss_feed Acompanhe os números deste periódico no seu leitor de RSS
Acessibilidade / Reportar erro