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During the congress, E-Posters will be accessible to all participants on the congress website 24/7, as well as in the E-poster stations in the congress center.
Preparing your E-Poster
Please review the E-Poster format requirements carefully when preparing your E-Poster. Should your E-Poster not meet the mentioned requirements, it may not be displayed as described above.
E-Poster Submission Deadline
Please prepare and upload your E-Poster no later than March 14, 2026 11.59PM CET. After this date, you will no longer be able to prepare and upload your E-poster and it will not be displayed and accessible on the congress website.
Please follow the instructions below to input your abstract title.
Abstract titles should be brief and reflect the content of the abstract.
Renal osteodystrophy (ROD) exhibits varying characteristics among different populations. Variable genetic and environmental factors and prescription patterns may explain these differences. Egyptian ROD is not sufficiently studied. Although bone biopsy is the gold standard tool, no single study has reported the actual ROD spectrum based on bone biopsy in Egypt or Africa.
The ISN-sistership program enabled us to create an Egyptian bone biopsy consortium that provided a nationwide specialized CKD-MBD service. Bone biopsies were planned based on clinical indications as bone pain, osteoporosis, or fractures that are not explained by non-invasive tools. In addition to basic clinical data, novel bone turnover biomarkers were done. Bone biopsies were analyzed under the supervision of experts from the University of Kentucky, USA.
Over 2 years, 14 patients consented to bone biopsy; all on HD. Adynamic bone disease (ABD) was the most common type of ROD in our cohort (50%). Unexpectedly, various degrees of +ve aluminum (AL) staining were present in 13 patients (93%) as shown in Table 1, despite the nonuse of AL-based phosphate binders.
To define a significant amount of AL toxicity, (AL+ve) group, 30% of the trabecular bone-osteoid interface stained with aluminum special stains was used as a cut-off point. AL+ve group included 8 patients (57%). Other biopsy findings are noted in Table 1 and Figures 2 and 3.
AL-induced suppression of bone cells was evident by low turnover biomarkers in patients with significant AL accumulation. Moreover, FGF-23 levels were significantly elevated in the AL+ group with a median of 2626 pg./mL compared to 1096 pg./mL in the AL- group (p-value = 0.041), as shown in Figure 4.
To conclude, AL bone disease is not extinct yet. 93% of the biopsied patients for clinical indications had variable degrees of positive aluminum staining, and 57% had significant aluminum accumulation. AL bone disease should be kept in its place in our differential diagnosis list of renal osteodystrophy.