Data comparing the efficacy of alfacalcidol to that of calcitriol in managing secondary hyperparathyroidism in patients with chronic kidney disease (CKD) is scarce. We sought to compare the efficacy of both drugs in managing hyperparathyroidism in patients with CKD. A retrospective observational cohort study conducted from January 2022 to March 2023 included adults with CKD stages 3 to 5 (non-dialysis) who received alfacalcidol for 3 months followed by calcitriol for another 3 months. Assessments were done at baseline and after 3 months of each treatment. The primary outcome was iPTH suppression, and the secondary outcome was total serum calcium levels. A total of 70 patients were included, with 34 (48.6%) being male. The cohort's mean age was 65.5 ± 15 years. CKD stage 3 comprised 47.1% of the sample. The median dose of alfacalcidol was 0.5 (0.25-0.8) µg compared to 0.5 (0.25-0.5) µg for calcitriol ( = .001). Alfacalcidol did not significantly suppress iPTH levels, with median values of 13.31 (8.23-24.4) pg/mL at baseline and 12.5 (8.86-24.7) pg/mL after 3 months ( = .937). In contrast, calcitriol significantly reduced iPTH levels from 12.5 (8.86-24.7) pg/mL to 10.7 (5.7-19) pg/mL ( = .017). Additionally, alfacalcidol did not significantly increase calcium levels, while calcitriol did. Throughout the study period, albumin values, the follow-up times, and the use of phosphate binders or non-active vitamin D remained consistent for each drug. The multivariate Generalized Estimating Equations indicated that baseline iPTH [ = 0.041, 95% CI (0.03- 0.05); < .001], calcitriol [ = -0.278, 95% CI (-0.5 to -0.06); = .014], daily dose of the study drug [ = -0.45, 95% CI (-0.7 to -0.2); < .001], and baseline phosphorus level [ = 0.354, 95% CI (0.004-0.7); = .047] were independent factors associated with iPTH suppression. Calcitriol, at significantly lower doses, was more effective than alfacalcidol in suppressing iPTH levels and increasing calcium levels over 3 months. A randomized controlled study is needed to confirm these findings.
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http://dx.doi.org/10.1177/00185787251322428 | DOI Listing |
Balkan J Med Genet
December 2024
Laboratory of Medical Biology - Genetics, Faculty of Medicine, School of Health Sciences, Aristotle University, Thessaloniki, Greece.
Primary hyperparathyroidism (PHPT) is a common endocrine disorder characterized by the overactivity of the parathyroid glands. While a few genes have been linked to a predisposition for PHPT, the genetic foundation of the disease remains unclear, despite it being the third most prevalent endocrine disorder. This pilot study aimed to investigate, for the first time, the potential association between specific variants in Annexin A2 (-rs7170178, rs17191344, rs11633032), Mediator Complex Subunit 12 (-rs1057519912), Calmodulin 1 (-rs12885713), and Mitogen-Activated Protein Kinase 1 (-rs1057519911) genes with PHPT.
View Article and Find Full Text PDFIndian J Otolaryngol Head Neck Surg
February 2025
Department of General Surgery, Amrita Institute of Medical Sciences, Amrita Hospitals, Kochi, Kerala India.
Despite the popularity of auto analyzers in urban areas of the country the incidence of asymptomatic hyperparathyroidism has not markedly increased and symptomatic diseases are regularly seen in all major institutions. The present single-institution analysis of proven hyperparathyroidism in the last 16 years was aimed at comparing the demographic, clinical, and pathological characteristics of symptomatic and asymptomatic primary hyperparathyroidism and comparing those with the asymptomatic diseases seen in developed countries. A retrospective chart review of 332 patients was done and 29 (8.
View Article and Find Full Text PDFEur J Endocrinol
March 2025
Department of Medicine, Division of Nephrology and Hypertension, University Hospitals of Geneva, Geneva, Switzerland.
Introduction: Primary hyperparathyroidism (PHPT) often causes hypercalcemia and complications requiring parathyroidectomy (PTX). Anemia affects 15-50% of PHPT patients, but its mechanisms remain unclear. While parathyroid hormone (PTH) and fibroblast growth factor 23 (FGF23) contribute to anemia in secondary hyperparathyroidism (SHPT) through erythropoietin (EPO) resistance and bone marrow fibrosis, their roles in PHPT are less defined.
View Article and Find Full Text PDFIndian J Otolaryngol Head Neck Surg
February 2025
AIIMS Bathinda Punjab, Bathinda, 151001 India.
Primary hyperparathyroidism is an endocrine disorder with muti-system involvement. The clinical condition is dealt by multi-speciality department. Parathyroid adenoma is the principal cause of primary hyperparathyroidism.
View Article and Find Full Text PDFIndian J Otolaryngol Head Neck Surg
February 2025
Department of Surgery, Command Hospital Air Force Bangalore, Bangalore, Karnataka 560007 India.
Secondary hyperparathyroidism (SHPT) is a common complication in chronic kidney disease patients, necessitating effective management to prevent adverse outcomes. This study evaluates the efficacy of surgical intervention in achieving biochemical balance in SHPT patients resistant to medical therapy. The study includes 36 patients with SHPT who underwent subtotal parathyroidectomy following failed medical management.
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