Detail
Článek
Článek online
FT
Medvik - BMČ
  • Je něco špatně v tomto záznamu ?

Assessment of Intrathecal Free Light Chain Synthesis: Comparison of Different Quantitative Methods with the Detection of Oligoclonal Free Light Chains by Isoelectric Focusing and Affinity-Mediated Immunoblotting

D. Zeman, P. Kušnierová, Z. Švagera, F. Všianský, M. Byrtusová, P. Hradílek, B. Kurková, O. Zapletalová, V. Bartoš,

. 2016 ; 11 (11) : e0166556. [pub] 20161115

Jazyk angličtina Země Spojené státy americké

Typ dokumentu srovnávací studie, časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc17023499

OBJECTIVES: We aimed to compare various methods for free light chain (fLC) quantitation in cerebrospinal fluid (CSF) and serum and to determine whether quantitative CSF measurements could reliably predict intrathecal fLC synthesis. In addition, we wished to determine the relationship between free kappa and free lambda light chain concentrations in CSF and serum in various disease groups. METHODS: We analysed 166 paired CSF and serum samples by at least one of the following methods: turbidimetry (Freelite™, SPAPLUS), nephelometry (N Latex FLC™, BN ProSpec), and two different (commercially available and in-house developed) sandwich ELISAs. The results were compared with oligoclonal fLC detected by affinity-mediated immunoblotting after isoelectric focusing. RESULTS: Although the correlations between quantitative methods were good, both proportional and systematic differences were discerned. However, no major differences were observed in the prediction of positive oligoclonal fLC test. Surprisingly, CSF free kappa/free lambda light chain ratios were lower than those in serum in about 75% of samples with negative oligoclonal fLC test. In about a half of patients with multiple sclerosis and clinically isolated syndrome, profoundly increased free kappa/free lambda light chain ratios were found in the CSF. CONCLUSIONS: Our results show that using appropriate method-specific cut-offs, different methods of CSF fLC quantitation can be used for the prediction of intrathecal fLC synthesis. The reason for unexpectedly low free kappa/free lambda light chain ratios in normal CSFs remains to be elucidated. Whereas CSF free kappa light chain concentration is increased in most patients with multiple sclerosis and clinically isolated syndrome, CSF free lambda light chain values show large interindividual variability in these patients and should be investigated further for possible immunopathological and prognostic significance.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc17023499
003      
CZ-PrNML
005      
20180503095009.0
007      
ta
008      
170720s2016 xxu f 000 0|eng||
009      
AR
024    7_
$a 10.1371/journal.pone.0166556 $2 doi
035    __
$a (PubMed)27846293
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xxu
100    1_
$a Zeman, David, $d 1972- $7 mzk2018988719 $u Institute of Laboratory Diagnostics, University Hospital Ostrava, 17. listopadu 1790, 708 52 Ostrava-Poruba, Czech Republic. Clinic of Neurology, University Hospital Ostrava, 17. listopadu 1790, 708 52 Ostrava-Poruba, Czech Republic.
245    10
$a Assessment of Intrathecal Free Light Chain Synthesis: Comparison of Different Quantitative Methods with the Detection of Oligoclonal Free Light Chains by Isoelectric Focusing and Affinity-Mediated Immunoblotting / $c D. Zeman, P. Kušnierová, Z. Švagera, F. Všianský, M. Byrtusová, P. Hradílek, B. Kurková, O. Zapletalová, V. Bartoš,
520    9_
$a OBJECTIVES: We aimed to compare various methods for free light chain (fLC) quantitation in cerebrospinal fluid (CSF) and serum and to determine whether quantitative CSF measurements could reliably predict intrathecal fLC synthesis. In addition, we wished to determine the relationship between free kappa and free lambda light chain concentrations in CSF and serum in various disease groups. METHODS: We analysed 166 paired CSF and serum samples by at least one of the following methods: turbidimetry (Freelite™, SPAPLUS), nephelometry (N Latex FLC™, BN ProSpec), and two different (commercially available and in-house developed) sandwich ELISAs. The results were compared with oligoclonal fLC detected by affinity-mediated immunoblotting after isoelectric focusing. RESULTS: Although the correlations between quantitative methods were good, both proportional and systematic differences were discerned. However, no major differences were observed in the prediction of positive oligoclonal fLC test. Surprisingly, CSF free kappa/free lambda light chain ratios were lower than those in serum in about 75% of samples with negative oligoclonal fLC test. In about a half of patients with multiple sclerosis and clinically isolated syndrome, profoundly increased free kappa/free lambda light chain ratios were found in the CSF. CONCLUSIONS: Our results show that using appropriate method-specific cut-offs, different methods of CSF fLC quantitation can be used for the prediction of intrathecal fLC synthesis. The reason for unexpectedly low free kappa/free lambda light chain ratios in normal CSFs remains to be elucidated. Whereas CSF free kappa light chain concentration is increased in most patients with multiple sclerosis and clinically isolated syndrome, CSF free lambda light chain values show large interindividual variability in these patients and should be investigated further for possible immunopathological and prognostic significance.
650    _2
$a studie případů a kontrol $7 D016022
650    _2
$a demyelinizační nemoci $x krev $x mok mozkomíšní $x diagnóza $7 D003711
650    _2
$a ELISA $x přístrojové vybavení $x metody $7 D004797
650    _2
$a lidé $7 D006801
650    _2
$a imunoblotting $x přístrojové vybavení $x metody $7 D015151
650    _2
$a imunoglobuliny - kappa-řetězce $x biosyntéza $x krev $x mok mozkomíšní $7 D007145
650    _2
$a imunoglobuliny - lambda-řetězce $x biosyntéza $x krev $x mok mozkomíšní $7 D007146
650    _2
$a isoelektrická fokusace $x přístrojové vybavení $x metody $7 D007525
650    _2
$a roztroušená skleróza $x krev $x mok mozkomíšní $x diagnóza $7 D009103
650    _2
$a nefelometrie a turbidimetrie $x přístrojové vybavení $x metody $7 D009391
650    _2
$a odchylka pozorovatele $7 D015588
650    _2
$a ROC křivka $7 D012372
650    _2
$a reprodukovatelnost výsledků $7 D015203
655    _2
$a srovnávací studie $7 D003160
655    _2
$a časopisecké články $7 D016428
700    1_
$a Kušnierová, Pavlína $u Institute of Laboratory Diagnostics, University Hospital Ostrava, 17. listopadu 1790, 708 52 Ostrava-Poruba, Czech Republic.
700    1_
$a Švagera, Zdeněk $u Institute of Laboratory Diagnostics, University Hospital Ostrava, 17. listopadu 1790, 708 52 Ostrava-Poruba, Czech Republic.
700    1_
$a Všianský, František $u Institute of Laboratory Diagnostics, University Hospital Ostrava, 17. listopadu 1790, 708 52 Ostrava-Poruba, Czech Republic.
700    1_
$a Byrtusová, Monika $u Institute for Healthcare Disciplines, St. Elisabeth University of Health and Social Work in Bratislava, Palackého 1, P.O. Box 104, 810 00 Bratislava, Slovak Republic.
700    1_
$a Hradílek, Pavel $u Clinic of Neurology, University Hospital Ostrava, 17. listopadu 1790, 708 52 Ostrava-Poruba, Czech Republic.
700    1_
$a Kurková, Barbora $u Clinic of Neurology, University Hospital Ostrava, 17. listopadu 1790, 708 52 Ostrava-Poruba, Czech Republic.
700    1_
$a Zapletalová, Olga $u Clinic of Neurology, University Hospital Ostrava, 17. listopadu 1790, 708 52 Ostrava-Poruba, Czech Republic.
700    1_
$a Bartoš, Vladimír $u Institute of Laboratory Diagnostics, University Hospital Ostrava, 17. listopadu 1790, 708 52 Ostrava-Poruba, Czech Republic.
773    0_
$w MED00180950 $t PloS one $x 1932-6203 $g Roč. 11, č. 11 (2016), s. e0166556
856    41
$u https://pubmed.ncbi.nlm.nih.gov/27846293 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20170720 $b ABA008
991    __
$a 20180503095129 $b ABA008
999    __
$a ok $b bmc $g 1239180 $s 984412
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2016 $b 11 $c 11 $d e0166556 $e 20161115 $i 1932-6203 $m PLoS One $n PLoS One $x MED00180950
LZP    __
$a Pubmed-20170720

Najít záznam

Citační ukazatele

Pouze přihlášení uživatelé

Možnosti archivace

Nahrávání dat ...