RT Journal Article
SR Electronic
T1 Gene Expression Pathways across Multiple Tissues in Antineutrophil Cytoplasmic Antibody-associated Vasculitis Reveal Core Pathways of Disease Pathology
JF The Journal of Rheumatology
JO J Rheumatol
FD The Journal of Rheumatology
SP 609
OP 615
DO 10.3899/jrheum.180455
VO 46
IS 6
A1 Marcia A. Friedman
A1 Dongseok Choi
A1 Stephen R. Planck
A1 James T. Rosenbaum
A1 Cailin H. Sibley
YR 2019
UL http://www.jrheum.org/content/46/6/609.abstract
AB Objective. To identify commonalities in gene expression data across all antineutrophil cytoplasmic antibody (ANCA)–associated vasculitis (AAV) tissues thus far characterized.Methods. Gene expression data were collected from the 3 AAV tissues thus far characterized (orbit, peripheral leukocytes, and sinus brushings). These data were analyzed to identify commonly expressed genes and disease pathways. The pathways data were adjusted for multiple comparisons using a combined local false discovery rate, which estimates the probability of a false discovery of a given pathway in all 3 tissues analyzed.Results. Only 4 genes were upregulated in all 3 tissues — IL1RN, TLR2, SLC11A1, and MMP9. After multiple comparison adjustments, the network pathway analysis revealed 28 pathways associated with all 3 tissues. The most strongly associated pathway for all 3 tissues was the neutrophil degranulation pathway [multidimensional local false discovery (md-locfdr) = 1.05 × 10−12], followed by the osteoclast differentiation (md-locfdr = 3.8 × 10−05), cell surface interactions at the vascular wall (md-locfdr = 4.2 × 10−04), signaling by interleukins (md-locfdr = 6.1 × 10−04), and phagosome (md-locfdr = 0.003) pathways. There were no downregulated genes or pathways common to all 3 tissues.Conclusion. This analysis identified individual genes and pathways of disease common to all AAV tissues thus far characterized. The use of a network pathway analysis allowed us to identify pathologic mechanisms that were not readily apparent in the commonly expressed genes alone. Many of these pathways are consistent with current theories about infectious drivers and the crossroads of innate and adaptive immune mechanisms. In addition, this analysis highlights novel pathways, such as vessel wall interactions and platelet activation, which require further investigation.