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Rigshospitalet - a part of Copenhagen University Hospital
E-pub ahead of print

The rheumatoid arthritis gene expression signature among women who improve or worsen during pregnancy - a pilot study

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OBJECTIVE: To assess whether gene expression signatures associated with rheumatoid arthritis (RA) before pregnancy differ between women who improve or worsen during pregnancy, and determine whether these expression signatures are altered during pregnancy when RA improves or worsens.

METHODS: Clinical data and blood samples were collected before pregnancy (T0) and at the third trimester (T3) from 11 RA and 5 healthy women. RA disease activity was assessed using the Clinical Disease Activity Index (CDAI). At each time-point, RA-associated gene expression signatures were identified using differential expression analysis of RNA sequencing profiles between RA and healthy women.

RESULTS: Of the women with RA, 6 improved by T3 (RAimproved), 3 worsened (RAworsened) and 2 were excluded. At T0, mean CDAI scores were similar in both groups (RAimproved: 11.2±9.8; RAworsened: 13.8±6.7; Wilcoxon-rank test: p=0.6). In the RAimproved group, 89 genes were differentially expressed at T0 (q<0.05 and fold-change (FC)≥2) compared to healthy women. When RA improved at T3, 65 of 89 (73%) of these no longer displayed RA-associated expression. In the RAworsened group, a largely different RA gene expression signature (429 genes) was identified at T0. When RA disease activity worsened at T3, 207 of 429 (48%) lost their differential expression, while an additional 157 genes became newly differentially expressed.

CONCLUSION: In our pilot dataset, pre-pregnancy RA expression signatures differed between women who subsequently improved or worsened during pregnancy, suggesting that inherent genomic differences perhaps influence how pregnancy impacts disease activity. Further, these RA signatures were altered during pregnancy, as disease activity changed.

Original languageEnglish
JournalJournal of Rheumatology
Publication statusE-pub ahead of print - 2021

Bibliographical note


ID: 61790980