The global antiphospholipid syndrome score in women with systemic lupus erythematosus and adverse pregnancy outcomes

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

  • K. Schreiber
  • M. Radin
  • I. Cecchi
  • E. Rubini
  • D. Roccatello
  • Jacobsen, Søren
  • M. J. Cuadrado
  • S. Sciascia

Objective To validate the global antiphospholipid syndrome score (GAPSS) in a cohort of women with systemic lupus erythematosus (SLE) and antiphospholipid antibodies (aPL). Methods This retrospective study included 143 women ever pregnant with SLE who presented in our outpatient clinic were included. Data on cardiovascular risk factors and aPL status were retrospectively collected and their individual GAPSS score was calculated. Results Significantly higher GAPSS values were found in women with any placental medicated complication (such as foetal death, placental abruption, prematurity, pre-eclampsia or intrauterine growth restriction (IUGR)) (GAPSS 8.2±3.0 vs. 3.5±3.0, p<0.001). Significantly higher GAPSS values were also found in those with recurrent miscarriages (RM) <10 weeks, foetal death, placental abruption, prematurity, pre-eclampsia or IUGR) (GAPSS 8.3±4.5 vs. 3.2±2.6, p<0.001). Patients with 3 or more consecutive early miscarriages (<10 weeks), foetal death, miscarriage <10 weeks gestation, premature birth (<34 weeks), pre-eclampsia (<34 weeks), stillbirth, and placental infarction had significantly higher GAPSS values compared to those without previous pregnancy complications. The odds ratio of having any pregnancy morbidity when having a GAPSS value ≥8 was 20 compared to those with a GAPSS of ≤1 (p<0.001). Conclusion Women with a history of aPL-related pregnancy complications had higher GAPSS values in this retrospective cohort compared to women without pregnancy complications. This study is the first step to assess the clinical utility of the GAPSS score in pregnancy. A prospective validation is needed.

OriginalsprogEngelsk
TidsskriftClinical and Experimental Rheumatology
Vol/bind39
Udgave nummer5
Sider (fra-til)1071-1076
Antal sider6
ISSN0392-856X
DOI
StatusUdgivet - 2021

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