Impact of pregnancy on progression of preclinical autoimmune disorders: a prospective cohort study

Rheumatology (Oxford)Published Prospective cohort study

Main finding · Progression to definite autoimmune diseaseResult — go to the resultAdjusted odds ratio 4.9 95% CI 2.4–10

Authors' conclusion

Among women with suspected autoimmune disease during pregnancy, additional viable pregnancies and diagnosis of preeclampsia were independently associated with an increased rate of progression to definite rheumatic disorder.

Study context

Population
Women with symptoms and laboratory findings suggestive of autoimmune disorder, enrolled in the first trimester of pregnancy
Participants
208 women
Exposure
One or more subsequent viable pregnancies vs no subsequent pregnancies
  • Subsequent pregnanciesn = 102
  • No subsequent pregnanciesn = 106reference
Outcome
Progression to definite autoimmune (rheumatic) disease
Follow-up
5 years
Methodological details5-year follow-up, multinomial logistic regression adjusted for confounders
  • 5-year follow-up
  • Multinomial logistic regression adjusted for confounders

Main finding

Progression to definite autoimmune disease

Adjusted odds ratio

4.9

95% CI 2.4–10

Events by group

Subsequent pregnanciesvs No subsequent pregnancies
aOR 4.9 (95% CI 2.4–10)

As reported in the abstract

Observational data: associations, not effects.

Further findings

Status at end of follow-up (all subjects) · 5 years

Negative
81 (38.9%)
Non-criteria rheumatic status
53 (25.5%)
Definite rheumatic disease
74 (35.6%)
Undifferentiated connective tissue disease
43
SLE
5
SS
3
APS
10
Miscellaneous autoimmune disorders
12

Time from enrolment to definite diagnosis

Median, months (IQR 18-42)
28

Preeclampsia (index or subsequent pregnancy) as risk factor for progression to definite autoimmune disease

aOR
4.3 (95% CI 1.2, 14.8)
  • Additional and independent risk factor

Original publication

Impact of pregnancy on progression of preclinical autoimmune disorders: a prospective cohort study. Rheumatology (Oxford). Published 7 November 2022. doi:10.1093/rheumatology/keac637

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