The establishment of specific reference intervals for serum transthyretin tetramer, misfolded proteins, and protein misfolding rate and its application in evaluating transthyretin amyloidosis patients

IF 2.9 3区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY Clinica Chimica Acta Pub Date : 2025-04-15 Epub Date: 2025-03-03 DOI:10.1016/j.cca.2025.120218
Tingting Wang , Ming Wu , Ying Wang , Ying Li , Xueting Cui , Xiaoyu Sun , Qiuhua Yu , Yunfeng Cao , Yu Liu , Zhuang Tian
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Abstract

Background

To accurately assess disease risk, specific reference intervals for transthyretin (TTR) tetramers, misfolded proteins, and protein misfolding rates are essential. This study aimed to establish reference intervals using a robust and traceable ultrahigh performance liquid chromatography (UPLC) method and to evaluate the distribution of these biomarkers in patients with transthyretin amyloidosis (ATTR).

Methods

Serum samples from 331 healthy Chinese individuals were included. Participants were stratified into two age groups: <60 years and ≥ 60 years. The reference intervals were determined following the Clinical and Laboratory Standards Institute (CLSI) EP28-A3.

Results

The established reference intervals for TTR tetramers, misfolded proteins, and protein misfolding rates revealed significant age- and sex-specific variations. In the < 60 years age group, the TTR tetramer reference intervals were 3.01–6.30 μmol/L for males and 2.62–5.39 μmol/L for females. Corresponding reference intervals for misfolded proteins were 0.24–1.43 μmol/L for males and 0.33–1.39 μmol/L for females, with protein misfolding rate upper limits of 26.32 % and 27.47 %, respectively. In the ≥ 60 years age group, TTR tetramer reference intervals from 2.56–5.48 μmol/L for males and 2.36–5.10 μmol/L for females. Misfolded protein reference intervals were 0.28–2.03 μmol/L for males and 0.29–1.59 μmol/L for females, while protein misfolding rate upper limits were 33.69 % for males and 30.64 % for females.

Conclusions

This study successfully established detailed, age- and sex-specific reference intervals for TTR tetramers, misfolded proteins, and protein misfolding rates, providing valuable references for clinical practice and further investigations into disease risk associated with TTR biomarkers.
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血清转甲状腺素四聚体、错误折叠蛋白、蛋白质错误折叠率特异性参考区间的建立及其在转甲状腺素淀粉样变患者评价中的应用
为了准确评估疾病风险,转甲状腺素(TTR)四聚体、错误折叠蛋白和蛋白质错误折叠率的特定参考区间是必不可少的。本研究旨在利用稳健、可追溯的超高高效液相色谱(UPLC)方法建立参考区间,并评估这些生物标志物在转甲状腺糖蛋白淀粉样变性(ATTR)患者中的分布。方法选取331名中国健康人群的血清样本。参与者被分为两个年龄组:60岁和≥60岁。参考区间按照临床和实验室标准协会(CLSI) EP28-A3确定。结果TTR四聚体、错误折叠蛋白和蛋白质错误折叠率的参考区间显示出明显的年龄和性别差异。在<;60岁年龄组,男性TTR四聚体参考区间为3.01 ~ 6.30 μmol/L,女性为2.62 ~ 5.39 μmol/L。错误折叠蛋白的参考区间雄性为0.24 ~ 1.43 μmol/L,雌性为0.33 ~ 1.39 μmol/L,错误折叠率上限分别为26.32%和27.47%。≥60岁年龄组,男性TTR四聚体参考区间为2.56 ~ 5.48 μmol/L,女性为2.36 ~ 5.10 μmol/L。错误折叠蛋白参考区间男性为0.28 ~ 2.03 μmol/L,女性为0.29 ~ 1.59 μmol/L,蛋白质错误折叠率上限男性为33.69%,女性为30.64%。本研究成功建立了TTR四聚体、错误折叠蛋白和蛋白质错误折叠率的详细的、年龄和性别特异性参考区间,为临床实践和进一步研究TTR生物标志物相关的疾病风险提供了有价值的参考。
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来源期刊
Clinica Chimica Acta
Clinica Chimica Acta 医学-医学实验技术
CiteScore
10.10
自引率
2.00%
发文量
1268
审稿时长
23 days
期刊介绍: The Official Journal of the International Federation of Clinical Chemistry and Laboratory Medicine (IFCC) Clinica Chimica Acta is a high-quality journal which publishes original Research Communications in the field of clinical chemistry and laboratory medicine, defined as the diagnostic application of chemistry, biochemistry, immunochemistry, biochemical aspects of hematology, toxicology, and molecular biology to the study of human disease in body fluids and cells. The objective of the journal is to publish novel information leading to a better understanding of biological mechanisms of human diseases, their prevention, diagnosis, and patient management. Reports of an applied clinical character are also welcome. Papers concerned with normal metabolic processes or with constituents of normal cells or body fluids, such as reports of experimental or clinical studies in animals, are only considered when they are clearly and directly relevant to human disease. Evaluation of commercial products have a low priority for publication, unless they are novel or represent a technological breakthrough. Studies dealing with effects of drugs and natural products and studies dealing with the redox status in various diseases are not within the journal''s scope. Development and evaluation of novel analytical methodologies where applicable to diagnostic clinical chemistry and laboratory medicine, including point-of-care testing, and topics on laboratory management and informatics will also be considered. Studies focused on emerging diagnostic technologies and (big) data analysis procedures including digitalization, mobile Health, and artificial Intelligence applied to Laboratory Medicine are also of interest.
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