Z Gastroenterol 2020; 58(08): e157
DOI: 10.1055/s-0040-1716155
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Serum IgG4 levels outperform IgG4/IgG RNA ratio in differential diagnosis of IgG4-related disease

L Schulte
Universitätsklinik Ulm, Innere Medizin 1, Ulm, Deutschland
,
F Arnold
Universitätsklinik Ulm, Innere Medizin 1, Ulm, Deutschland
,
F Siegel
Universitätsklinik Ulm, Innere Medizin 1, Ulm, Deutschland
,
J Backhus
Universitätsklinik Ulm, Innere Medizin 1, Ulm, Deutschland
,
L Perkhofer
Universitätsklinik Ulm, Innere Medizin 1, Ulm, Deutschland
,
A Beutel
Universitätsklinik Ulm, Innere Medizin 1, Ulm, Deutschland
,
M Müller
Universitätsklinik Ulm, Innere Medizin 1, Ulm, Deutschland
,
A Kleger
Universitätsklinik Ulm, Innere Medizin 1, Ulm, Deutschland
› Institutsangaben
 

IgG4-related disease (IgG4-RD) is a chronic inflammatory-fibrosing disorder affecting virtually any organ, but most frequently the pancreaticobiliary system. Differential diagnosis is challenging due to a highly variable clinical presentation and relies on multiple diagnostic criteria rather than on single markers. Previously, qPCR-based measurements of the IgG4/IgG mRNA ratio that originate from dominant IgG4+ B-cell receptor (BCR) clones have been propagated as a critical endeavor to fill this diagnostic gap. In the current study, we demonstrated in concordance with de Vires et al. on independent cohorts and with different methodological setups that IgG4/IgG mRNA ratio is prone to false-positive results, which could cause misdiagnosis of pancreaticobiliary cancer. Furthermore, we found superior test accuracy of serum IgG4 levels, likewise not a perfect biomarker itself. Therefore, our study questions the clinical benefit of IgG4/IgG mRNA ratios in the differential diagnosis of IgG4-RD in support of de Vires et al. but concurrently underpins the necessity for more reliable biomarkers to differentially diagnose IgG4-RD.



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Artikel online veröffentlicht:
08. September 2020

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