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CONTRIBUTI SCIENTIFICI – Scientific Papers

Volume:

Biochimica Clinica, 48 (3) pag 239-246

Pubblicato on-line:

June 5, 2024

DOI:

10.19186/BC_2024.029

Scarica in PDF:
Autenticazione richiesta

Transtiretina e Proteina legante il retinolo 4: una valutazione analitica del metodo immunonefelometrico

AUTORI

Veronica Musetti1, Chiara Sanguinetti2, Silvia Masotti3, Carmen Corciulo3, Federico Bigazzi3, Concetta Prontera3, Vincenzo Castiglione1,3, Alberto Aimo1,3, Giuseppe Vergaro1,3, Michele Emdin1,3, Maria Franzini2
1Centro di ricerca interdisciplinare Health Science, Scuola Superiore Sant’Anna, Pisa
2Dipartimento di Ricerca traslazionale e Nuove tecnologie in Medicina e Chirurgia, Università di Pisa
3Fondazione Toscana G. Monasterio, Pisa

ABSTRACT

Transthyretin and Retinol binding protein 4: analytical evaluation of the immunonephelometric method

Introduction: transthyretin cardiac amyloidosis (ATTR-CA) is a progressive disease in which circulating levels of TTR contribute to risk stratification of disease progression and represent a biomarker of response to therapy. Aim of this study is to evaluate the analytical characteristics of the nephelometric method used to measure TTR and Retinol binding protein 4 (RBP4).
Methods: paired serum (S) and plasma lithium heparin (Li-ep) samples from healthy subjects and patients with ATTR-CA were collected. Reproducibility analysis, based on the CSLI EP05-A3 protocol, was conducted using S and Li-ep pools where TTR and RBP4 were measured on the automated system Atellica NEPH 630 (Siemens Healthineers). S and Li-ep pools were analysed also by a native electrophoresis on 4-20% polyacrylamide gel associated with western-blot for TTR and RBP4.
Results: no differences were observed in the measurement of TTR and RBP4 in Li-ep and S. The nephelometric method had a similar analytical performance in both matrices (CV% repeatability Li-ep and S: TTR 1.92 and 2.52; RBP4 2.25 and 1.49; CV% within lab-precision: TTR 2.40 and 2.90; RBP4 2.30 and 2.14). Electrophoresis highlighted the presence of high molecular weight forms, TTR tetramers bound to 1 or 2 RBP4 and TTR trimers and dimers in both matrices.
Conclusion: measurement of circulating TTR and RBP4 can be performed on both Li-ep and S. The evaluation of the nephelometric assay showed suitable performances to use it in the clinical context of ATTR-CA. Electrophoretic investigations revealed the presence of several TTR circulating forms, thus further studies are necessary to understand which one is quantified by nephelometry.

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