Reliable typing of systemic amyloidoses through proteomic analysis of subcutaneous adipose tissue

被引:145
作者
Brambilla, Francesca [2 ]
Lavatelli, Francesca [3 ]
Di Silvestre, Dario [2 ]
Valentini, Veronica
Rossi, Rossana [2 ]
Palladini, Giovanni [4 ]
Obici, Laura
Verga, Laura [6 ]
Mauri, Pierluigi [2 ]
Merlini, Giampaolo [1 ,4 ,5 ]
机构
[1] Fdn IRCCS Policlin San Matteo, Amyloid Res & Treatment Ctr, I-27100 Pavia, Italy
[2] Consiglio Nazl Ric Ist Tecnol Biomed, Milan, Italy
[3] Univ Pavia, Biomed Informat Lab, I-27100 Pavia, Italy
[4] Univ Pavia, Dept Biochem, I-27100 Pavia, Italy
[5] Policlin San Matteo, Fdn Ist Ricovero & Cura Carattere Sci, Clin Chem Labs, I-27100 Pavia, Italy
[6] Policlin San Matteo, Fdn Ist Ricovero & Cura Carattere Sci, Dept Pathol, I-27100 Pavia, Italy
关键词
PROTEIN IDENTIFICATION TECHNOLOGY; RNA DEGRADOSOME COMPOSITION; ESCHERICHIA-COLI; FAT TISSUE; DEPOSITS; AL;
D O I
10.1182/blood-2011-07-365510
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Considering the important advances in treating specific types of systemic amyloidoses, unequivocal typing of amyloid deposits is now essential. Subcutaneous abdominal fat aspiration is the easiest, most common diagnostic procedure. We developed a novel, automated approach, based on Multidimensional Protein Identification Technology, for typing amyloidosis. Fat aspirates were obtained from patients with the most common systemic amyloidoses (AL lambda, AL kappa, transthyretin, and reactive amyloidosis), with Congo red score more than or equal to 3+, and nonaffected controls. Peptides from extracted and digested proteins were analyzed by Multidimensional Protein Identification Technology. On semiquantitative differential analysis (patients vs controls) of mass spectrometry data, specific proteins up-represented in patients were identified and used as deposit biomark-ers. An algorithm was developed to classify patients according to type and abundance of amyloidogenic proteins in samples; in all cases, proteomic characterization was concordant with fibril identification by immunoelectron microscopy and consistent with clinical presentation. Our approach allows reliable amyloid classification using readily available fat aspirates. (Blood. 2012;119(8):1844-1847)
引用
收藏
页码:1844 / 1847
页数:4
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