# Pregnancy outcomes in idiopathic inflammatory myopathies: a Portuguese multicentre study

**Authors:** Ana Rita Lopes, Ana Teodósio Chícharo, Raquel Campanilho-Marques, Catarina Abreu, Sara Dias Rodrigues, Inês Santos, Filipa Paramés, Sofia C. Barreira, Maria Pulido-Valente, Luísa Pinto, Ana Rita Cruz-Machado, Susana Capela

PMC · DOI: 10.3389/fmed.2025.1724170 · Frontiers in Medicine · 2025-12-19

## TL;DR

This study examines pregnancy outcomes in women with inflammatory myopathies, finding that disease activity is a major factor in adverse outcomes.

## Contribution

The study provides new insights into the relationship between disease activity and adverse pregnancy outcomes in idiopathic inflammatory myopathies.

## Key findings

- Adverse pregnancy outcomes occurred in 50% of cases, primarily linked to disease flares.
- Anti-Jo-1 positivity was associated with more severe outcomes like stillbirth and fetal growth restriction.
- Remission at conception did not fully prevent obstetric complications in some pregnancies.

## Abstract

Idiopathic inflammatory myopathies (IIM) are rare autoimmune diseases that may complicate pregnancy, but evidence remains scarce. Disease activity at conception and during gestation, together with autoantibody profiles, are considered major determinants of adverse pregnancy outcomes (APOs).

We conducted a retrospective multicentre study of 12 pregnancies in 10 women with IIM followed at four Portuguese tertiary centers (2009–2025). Demographic, clinical, immunological, therapeutic, maternal, and perinatal data were collected from medical records. Disease activity was assessed by clinical features, laboratory data, modified skin Disease Activity Score, and Manual Muscle Testing-8.

Phenotypes included overlap myositis (n = 4), antisynthetase syndrome (n = 3), dermatomyositis (n = 3), immune-mediated necrotising myopathy (n = 1), and polymyositis (n = 1). Myositis-specific/associated autoantibodies were detected in 91.7% of the cases, most frequently anti-Ro52 and anti-Jo-1. Disease remission at conception was documented in nine pregnancies (75.0%). Overall, APOs occurred in six pregnancies (50.0%): four miscarriages, one stillbirth, and one fetal growth restriction (FGR) with a small-for-gestational-age neonate. Of the 12 pregnancies, seven resulted in live births. All APOs occurred in pregnancies with disease flares, none occurred when disease remained stable. Among pregnancies with known preconception status, APOs occurred both in pregnancies conceived under active disease and in some conceived during remission. The most severe outcomes (stillbirth, FGR) occurred in one mother with antisynthetase syndrome and markedly elevated anti-Jo-1 titres. No cases of preeclampsia, eclampsia, congenital anomalies, or neonatal lupus were observed.

In this cohort, APOs were frequent, particularly among pregnancies complicated by disease activity. Although remission at conception was common, it did not fully prevent flares or obstetric complications. Anti-Jo-1 positivity appeared to cluster among the more severe cases, suggesting potential clinical relevance for monitoring. Multidisciplinary care and preconception optimization remain essential. Larger multicentre registries will be crucial to improving understanding and management of pregnancy in IIM.

## Linked entities

- **Diseases:** idiopathic inflammatory myopathies (MONDO:0020122), antisynthetase syndrome (MONDO:0019344), dermatomyositis (MONDO:0016367), polymyositis (MONDO:0019127), preeclampsia (MONDO:0005081), eclampsia (MONDO:0001754), neonatal lupus (MONDO:0018360)

## Full-text entities

- **Genes:** TRIM21 (tripartite motif containing 21) [NCBI Gene 6737] {aka RNF81, RO52, Ro/SSA, SSA, SSA1, TRIM21/Ro52}
- **Diseases:** dermatomyositis (MESH:D003882), necrotising myopathy (MESH:D019283), polymyositis (MESH:D017285), preeclampsia (MESH:D011225), congenital anomalies (MESH:D000013), autoimmune diseases (MESH:D001327), IIM (MESH:D009220), skin Disease (MESH:D012871), antisynthetase syndrome (MESH:C537778), FGR (MESH:D005317), stillbirth (MESH:D050497), eclampsia (MESH:D004461), neonatal lupus (MESH:C536397)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

30 references — full list in the complete paper: https://tomesphere.com/paper/PMC12758025/full.md

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Source: https://tomesphere.com/paper/PMC12758025