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Biochemical Clusters as Substitutes of Bone Biopsies in Kidney Transplant Patients.

dc.contributor.authorFerreira, Ana Carina
dc.contributor.authorMendes, Marco
dc.contributor.authorSilva, Cecília
dc.contributor.authorCotovio, Patrícia
dc.contributor.authorAires, Inês
dc.contributor.authorNavarro, David
dc.contributor.authorCaeiro, Fernando
dc.contributor.authorSalvador, Rute
dc.contributor.authorCorreia, Bruna
dc.contributor.authorCabral, Guadalupe
dc.contributor.authorNolasco, Fernando
dc.contributor.authorFerreira, Aníbal
dc.date.accessioned2025-07-24T10:05:23Z
dc.date.available2025-07-24T10:05:23Z
dc.date.issued2024-03
dc.description.abstractBone and mineral metabolism abnormalities are frequent in kidney transplant recipients and have been associated with cardiovascular morbidity. The primary aim of this study was to analyse the association between routine clinically available biochemical evaluation, non-routine histomorphometric bone evaluation, and vascular disease in kidney transplanted patients. A cross-sectional analysis was performed on 69 patients, 1-year after kidney transplantation. Laboratory analysis, radiography of hands and pelvis, bone biopsy, bone densitometry, and coronary CT were performed. One-year post-transplantation, nearly one-third of the patients presented with hypercalcemia, 16% had hypophosphatemia, 39.3% had iPTH levels > 150 pg/mL, 20.3% had BALP levels > 40 U/L, and 26.1% had hypovitaminosis D. Evaluation of extraosseous calcifications revealed low Adragão and Agatston scores. We divided patients into three clusters, according to laboratory results routinely used in clinical practice: hypercalcemia and hyperparathyroidism (Cluster1); hypercalcemia and high BALP levels (Cluster2); hypophosphatemia and vitamin D deficiency (Cluster 3). Patients in clusters 1 and 2 had higher cortical porosity (p = 0.001) and osteoid measurements, although there was no difference in the presence of abnormal mineralization, or low volume. Patients in cluster 2 had a higher BFR/BS (half of the patients in cluster 2 had high bone turnover), and most patients in cluster 1 had low or normal bone turnover. Cluster 3 has no differences in volume, or turnover, but 60% of the patients presented with pre-osteomalacia. All three clusters were associated with high vascular calcifications scores. Vascular calcifications scores were not related to higher bone mineral density. Instead, an association was found between a higher Adragão score and the presence of osteoporosis at the femoral neck (p = 0.008). In conclusion, inferring bone TMV by daily clinical biochemical analysis can be misleading, and bone biopsy is important for assessing both bone turnover and mineralization after kidney transplantation, although hypophosphatemia combined with vitamin D deficiency is associated with abnormal mineralization. The presence of hypercalcemia with high levels of PTH or high levels of BALP, or hypophosphatemia and vitamin D deficiency should remind us to screen vascular calcification status of patients.Clinical Research: ClinicalTrials.gov ID NCT02751099.eng
dc.identifier.citationCalcif Tissue Int . 2024 Mar;114(3):267-275
dc.identifier.doi10.1007/s00223-023-01173-1
dc.identifier.other38253933
dc.identifier.urihttp://hdl.handle.net/10400.17/5115
dc.language.isoen
dc.peerreviewedyes
dc.publisherSpringerlink
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.subjectBiochemical analysis
dc.subjectBone biopsies
dc.subjectMineralization defects
dc.subjectVascular calcifications
dc.subjectHCC NEF
dc.titleBiochemical Clusters as Substitutes of Bone Biopsies in Kidney Transplant Patients.
dc.typetext
dspace.entity.typePublication
oaire.citation.endPage275
oaire.citation.issue3
oaire.citation.startPage267
oaire.citation.volume114
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85

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