Cleavage of cystatin C is not associated with multiple sclerosis

被引:29
作者
Del Boccio, Piero
Pieragostino, Damiana
Lugaresi, Alessandra
Di Ioia, Maria
Pavone, Barbara
Travaglini, Daniela
D'Aguanno, Simona
Bernardini, Sergio
Sacchetta, Paolo
Federici, Giorgio
Di Ilio, Carmine
Gambi, Domenico
Urbani, Andrea
机构
[1] Univ G dAnnunzio, Ctr Excellence Aging, CeSI, Fdn G Dannunzio, I-66100 Chieti, Italy
[2] Univ G Dannunzio Chieti & Pescare, Dipartimento Sci BioMed, Chieti, Italy
[3] IRCCS, Fdn S Lucia, Ctr Europeo Ric Cervello, Rome, Italy
[4] Univ G Dannunzio Chieti & Pescare, Dipartimento Oncol & Neurosci, Chieti, Italy
[5] Univ Roma Tor Vergata, Dipartimento Med Interna, Rome, Italy
关键词
D O I
10.1002/ana.20968
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Recently, Irani and colleagues proposed a C-terminal cleaved isoform cystatin C (12.5kDa) in cerebrospinal fluid as a marker of multiple sclerosis. In this study, we demonstrate that the 12.5kDa product of cystatin C is formed by degradation of the first eight N-terminal residues. Moreover, such a degradation is not specific in the cerebrospinal fluid of multiple sclerosis, but rather is given by an inappropriate sample storage at -20 degrees C. We conclude that the use of the 12.5kDa product of cystatin C in cerebrospinal fluid might lead to a fallacious diagnosis of multiple sclerosis. Preanalytical validation procedure is mandatory for proteomics investigations.
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收藏
页码:201 / 204
页数:4
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