The Impact of Cholecaciferol Supplementation on Bone Mineral Density in Long-Term Kidney Transplant Recipients

被引:4
作者
Battaglia, Yuri [1 ,2 ]
Bellasi, Antonio [3 ]
Esposito, Pasquale [4 ]
Bortoluzzi, Alessandra [5 ]
Rotondi, Silverio [6 ]
Andreucci, Michele [7 ]
Fiorini, Fulvio [8 ]
Russo, Domenico [9 ]
Storari, Alda [10 ]
机构
[1] Univ Verona, Dept Med, I-37129 Verona, Italy
[2] Pederzoli Hosp, Nephrol & Dialysis Unit, I-37019 Verona, Italy
[3] Ente Osped Cantonale, Nephrol Unit, CH-6900 Lugano, Switzerland
[4] Univ Genoa, IRCCS Osped Policlin San Martino, Div Nephrol Dialysis & Transplantat, I-16132 Genoa, Italy
[5] Univ Ferrara, Dept Med Sci, Rheumatol Unit, I-44124 Ferrara, Italy
[6] Sapienza Univ Rome, Dept Translat & Precis Med, I-00185 Rome, Italy
[7] Magna Graecia Univ Catanzaro, Dept Hlth Sci, Nephrol & Dialysis Unit, I-88100 Catanzaro, Italy
[8] Santa Maria della Misericordia Hosp, Div Nephrol & Dialysis, I-45100 Rovigo, Italy
[9] Univ Federico II, Dept Publ Hlth, I-80100 Naples, Italy
[10] St Anna Univ Hosp, Nephrol & Dialysis Unit, I-44124 Ferrara, Italy
关键词
bone mineral disease; vitamin D; kidney transplantation; Z-score; T-score; femoral neck; lumbar vertebral bodies; DEXA; KDIGO guidelines; VITAMIN-D; DISEASE; BIOPSIES; THERAPY;
D O I
10.3390/biom13040629
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Although reduced bone mineral density (BMD) is associated with a higher risk of fractures, morbidity, and mortality in kidney transplant patients (KTRs), there is no consensus on optimal treatment for the alterations of BMD in this population. This study aims at assessing the effect of cholecalciferol supplementation on BMD over a follow-up period of 2 years in a cohort of long-term KTRs. Patients with age >= 18 years were included and divided into two subgroups based on treatment with bisphosphonate and/or calcimimetics and/or active vitamin D sterols (KTRs-treated) or never treated with the above medications (KTRs-free). BMD was evaluated at lumbar vertebral bodies (LV) and right femoral neck (FN) with standard DEXA at the beginning and end of the study. According to World Health Organization (WHO) criteria, results were expressed as T-score and Z-score. Osteoporosis and osteopenia were defined as T score <= -2.5 SD and T score < -1 and >-2.5 SD, respectively. Cholecalciferol was supplemented at a dose of 25,000 IU/week over 12 weeks followed by 1500 IU/day. KTRs-free (n. 69) and KTRs-treated (n. 49) consecutive outpatients entered the study. KTRs-free were younger (p < 0.05), with a lower prevalence of diabetes (p < 0.05) and of osteopenia at FN (46.3 % vs. 61.2 %) compared to KTRs-treated. At the entry none of the study subjects had a sufficient level of cholecalciferol; Z-score and T-score at LV and FN were not different between groups. At the end of the study period, serum cholecalciferol concentration was significantly increased in both groups (p < 0.001); the KTRs-free group presented an improvement in both T-score and Z-score at LV (p < 0.05) as well as a lower prevalence of osteoporotic cases (21.7% vs. 15.9%); in contrast, no changes were recorded in KTR-treated individuals. In conclusion, supplementation with cholecalciferol ameliorated Z-score and T-score at LV in long-term KTRs who had been never treated with active or inactive vitamin D sterols, bisphosphonates, and calcimimetics. Future endeavours are needed to confirm these preliminary findings.
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页数:10
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