Comparison of second and third-generation parathyroid hormone assays at a tertiary hospital in South Africa.

IF 1.2 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
African Journal of Laboratory Medicine Pub Date : 2025-08-30 eCollection Date: 2025-01-01 DOI:10.4102/ajlm.v14i1.2700
Nokuthula Nhlapo, Doreen Jacob, Siyabonga Khoza, Mpho R Maphayi
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引用次数: 0

Abstract

Background: Parathyroid hormone (PTH) measurement is key for diagnosing parathyroid disorders, and for management of chronic kidney disease. Available PTH assays include second (intact PTH) and third (PTH 1-84) generations. Data comparing interchangeable use are insufficient.

Objective: The objective of this study was to compare intact and 1-84 PTH assays to determine the difference in analytical performance and impact on clinical interpretation.

Methods: A method comparison was done on residual samples with PTH requests (06 April 2022 - 21 September 2022) from a tertiary hospital in South Africa. Parathyroid hormone was measured using both intact PTH and 1-84 PTH assays. Clinical performance was compared in the diagnosis of hypo- and hyperparathyroidism, and in pre-dialysis and dialysis chronic kidney disease patients.

Results: Among 481 samples, intact PTH had a higher median concentration than PTH 1-84 (9.85 pmol/L vs. 8.51 pmol/L, p < 0.0001), but the two showed good correlation (r = 0.994, p < 0.0001). Regression analysis revealed systematic (intercept = 0.887 pmol/L [95% confidence interval: 0.788 - 1.005]) and proportional differences (slope = 0.713 pmol/L, [95% confidence interval: 0.703 - 0.723]), with increased deviations at higher concentrations. The average bias was 18.5%, exceeding allowable limits. Among the 276 patients (170 women, 106 men, age range: 18-89 years) included in the clinical study, interpretation was unchanged.

Conclusion: A bias was observed between the PTH assays, indicating that they should not be used interchangeably. However, no changes in clinical interpretation were observed when one assay was used over the other.

What this study adds: The study confirms the recommendation by Kidney Disease: Improving Global Outcomes for the use of assay-specific upper limit of normal instead of generic cut-off in dialysis patients. This study further highlights the need for standardisation of PTH assays.

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南非一家三级医院第二代和第三代甲状旁腺激素测定的比较。
背景:甲状旁腺激素(PTH)测量是诊断甲状旁腺疾病和治疗慢性肾脏疾病的关键。可用的PTH检测包括第二代(完整PTH)和第三代(PTH 1-84)。比较可互换使用的数据不足。目的:本研究的目的是比较完整和1-84甲状旁腺激素测定,以确定分析性能的差异和对临床解释的影响。方法:对南非某三级医院(2022年4月6日- 2022年9月21日)PTH请求残留样本进行方法比较。甲状旁腺激素采用完整PTH和1-84 PTH测定。比较透析前和透析后慢性肾病患者甲状旁腺功能低下和甲状旁腺功能亢进诊断的临床表现。结果:在481份样本中,完整PTH的中位浓度高于PTH 1-84 (9.85 pmol/L vs. 8.51 pmol/L, p < 0.0001),但两者具有良好的相关性(r = 0.994, p < 0.0001)。回归分析显示系统差异(截距= 0.887 pmol/L[95%置信区间:0.788 ~ 1.005])和比例差异(斜率= 0.713 pmol/L,[95%置信区间:0.703 ~ 0.723]),浓度越高,偏差越大。平均偏差为18.5%,超出允许范围。在纳入临床研究的276例患者(女性170例,男性106例,年龄范围:18-89岁)中,解释不变。结论:观察到甲状旁腺激素测定之间存在偏差,表明它们不应互换使用。然而,当使用一种检测方法时,没有观察到临床解释的变化。本研究补充的内容:该研究证实了《肾脏疾病:改善全球结局》(Kidney Disease: improvement Global Outcomes)的建议,即在透析患者中使用测定特异性的正常上限,而不是通用的临界值。本研究进一步强调了甲状旁腺激素检测标准化的必要性。
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
African Journal of Laboratory Medicine
African Journal of Laboratory Medicine MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
1.70
自引率
9.10%
发文量
53
审稿时长
12 weeks
期刊介绍: The African Journal of Laboratory Medicine, the official journal of ASLM, focuses on the role of the laboratory and its professionals in the clinical and public healthcare sectors,and is specifically based on an African frame of reference. Emphasis is on all aspects that promote and contribute to the laboratory medicine practices of Africa. This includes, amongst others: laboratories, biomedical scientists and clinicians, medical community, public health officials and policy makers, laboratory systems and policies (translation of laboratory knowledge, practices and technologies in clinical care), interfaces of laboratory with medical science, laboratory-based epidemiology, laboratory investigations, evidence-based effectiveness in real world (actual) settings.
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