Evaluation of the age-specific relationship between PTH and vitamin D metabolites

IF 2.1 Q3 ENDOCRINOLOGY & METABOLISM
Alexandra Povaliaeva , Artem Zhukov , Viktor Bogdanov , Axenia Bondarenko , Oleg Senko , Anna Kuznetsova , Maxim Kodryan , Vitaliy Ioutsi , Ekaterina Pigarova , Liudmila Rozhinskaya , Natalia Mokrysheva
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引用次数: 0

Abstract

A commonly used method for determining vitamin D sufficiency is the suppression of excess PTH secretion. Conventionally, the main circulating vitamin D metabolite 25(OH)D is used for this assessment, however, the cut-off data for this parameter vary widely in the literature. The role of other metabolites as markers of vitamin D status is actively debated. The aim of our study was to assess the relationship between PTH, age and parameters characterizing vitamin D status, both “classical” – 25(OH)D3, and “non-classical” – 24,25(OH)2D3 and 25(OH)D3/24,25(OH)2D3 (vitamin D metabolite ratio, VMR). This prospective non-controlled cohort study included 162 apparently healthy Caucasian adult volunteers. When PTH was binarized according to the median value, at VMR < 14.9, 25(OH)D3 > 9.7 ng/mL and 24,25(OH)2D3 > 0.64 ng/mL there was a pronounced relationship between PTH and age (p = 0.001, p = 0.023 and p = 0.0134 respectively), with the prevalence of higher PTH levels in older individuals and vice versa. Moreover, at an age of <40.3 years, there was a pronounced relationship between PTH and VMR (p < 0.001), and similarly at an age of <54.5 years, there was a pronounced relationship between PTH and 25(OH)D3 (p = 0.002) as well as between PTH and 24,25(OH)2D3 (p = 0.0038): in younger people, higher PTH values prevailed only in the range of vitamin D insufficiency, while in the older age group this relationship was not demonstrated and PTH values were in general above the median. VMR controlled the correlation between PTH and age more strongly than metabolites 25(OH)D3 and 24,25(OH)2D3 (p = 0.0012 vs. p > 0.05 and p = 0.0385 respectively). The optimal threshold was found equal to 11.7 for VMR such that the relationship between PTH and age in the subset of participants with VMR < 11.7 was characterized by a correlation coefficient of ρ = 0.68 (p < 0.001), while the cohort with VMR > 11.7 was characterized by a very weak correlation coefficient of ρ = 0.12 (p = 0.218), which is non-significant. In summary, our findings suggest that the relationship between PTH and vitamin D is age-dependent, with a greater susceptibility to elevated PTH among older individuals even with preserved renal function, likely due to the resistance to vitamin D function. We propose VMR can be considered as a potential marker of vitamin D status. These findings require confirmation in larger population-based studies.

评估 PTH 与维生素 D 代谢物之间的特定年龄关系
确定维生素 D 是否充足的常用方法是抑制过多的 PTH 分泌。传统上,主要的循环维生素 D 代谢物 25(OH)D 被用于这一评估,但文献中该参数的临界数据差异很大。关于其他代谢物作为维生素 D 状态标志物的作用,目前还存在激烈的争论。我们的研究旨在评估 PTH、年龄和表征维生素 D 状态的参数之间的关系,包括 "经典"--25(OH)D3 和 "非经典"--24,25(OH)2D3 和 25(OH)D3/24,25(OH)2D3(维生素 D 代谢物比值,VMR)。这项前瞻性非对照队列研究包括 162 名表面健康的高加索成年志愿者。当根据中值对 PTH 进行二值化处理时,VMR 为 14.9,25(OH)D3 为 9.7 纳克/毫升,24,25(OH)2D3 为 0.64 纳克/毫升,PTH 与年龄之间存在明显的关系(分别为 p = 0.001、p = 0.023 和 p = 0.0134),年龄越大,PTH 水平越高,反之亦然。此外,在年龄为 40.3 岁时,PTH 与 VMR 之间存在明显的关系(p = 0.001);同样,在年龄为 54.5 岁时,PTH 与 25(OH)D3 之间存在明显的关系(p = 0.002)以及 PTH 和 24,25(OH)2D3 之间的关系(p = 0.0038):在年轻人中,只有在维生素 D 不足的范围内才会出现较高的 PTH 值,而在老年人群中,这种关系并不明显,PTH 值一般都高于中位数。VMR 比代谢物 25(OH)D3 和 24,25(OH)2D3(分别为 p = 0.0012 vs. p > 0.05 和 p = 0.0385)更能控制 PTH 与年龄之间的相关性。VMR 的最佳阈值为 11.7,因此,在 VMR 为 11.7 的参与者中,PTH 与年龄之间的相关系数为 ρ = 0.68(p = 0.001),而 VMR 为 11.7 的参与者中,PTH 与年龄之间的相关系数为 ρ = 0.12(p = 0.218),相关性很弱,不显著。总之,我们的研究结果表明,PTH 和维生素 D 之间的关系与年龄有关,即使肾功能保持良好,老年人也更容易出现 PTH 升高,这可能是由于维生素 D 功能的阻力所致。我们建议将 VMR 视为维生素 D 状态的潜在标志物。这些发现需要在更大规模的人群研究中得到证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Bone Reports
Bone Reports Medicine-Orthopedics and Sports Medicine
CiteScore
4.30
自引率
4.00%
发文量
444
审稿时长
57 days
期刊介绍: Bone Reports is an interdisciplinary forum for the rapid publication of Original Research Articles and Case Reports across basic, translational and clinical aspects of bone and mineral metabolism. The journal publishes papers that are scientifically sound, with the peer review process focused principally on verifying sound methodologies, and correct data analysis and interpretation. We welcome studies either replicating or failing to replicate a previous study, and null findings. We fulfil a critical and current need to enhance research by publishing reproducibility studies and null findings.
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