Table 1

Characteristics of study population

CharacteristicsControl
(n=10)
Pre-eclampsia
(N=11)
SLE
(N=10)
SLE+pre-eclampsia
(N=4)
Maternal
 Age at delivery (mean; SD)35.5 (4.12)29 (4.98)31.7 (5.93)31.5 (7.77)
Race
 White (not Hispanic)5 (50%)6 (55%)7 (70%)4 (100%)
 African/African–American2 (20%)1 (9%)2 (20%)0
 Asian2 (20%)3 (27%)00
 Hispanic01 (9%)1 (10%)0
 Multiracial1 (10%)000
 Delivery by caesarean- section9 (90%)9 (82%)7 (70%)1 (25%)
 SLE active during pregnancy*n/an/a1 (10%)1 (25%)
Medications during pregnancy†
 Azathioprinen/an/a4 (40%)0
 Hydroxychloroquinen/an/a5 (50%)0
 SQ heparin and/or 81 mg aspirinn/an/a6 (60%)4 (100%)
 Daily prednisone4 (40%)2 (60%)
 APSn/an/a‡3 (30%)1 (25%)
 ANA+1 (9%)10 (100%)4 (100%)
 APLAb+5 (50%)1 (25%)
 ENA+4 (40%)1 (25%)
Child
 Weight, g (mean; SD)3505 (264.82)2020.36 (1055.97)2920.1 (699.33)1495 (1190.4)§
 Gestational age, weeks (median; IQR)39.15 (0.35)35 (8.4)36.39 (2.55)30 (5.88)¶
 Duration ROM (median; IQR)n/a0 (0)1 (511)94 (94)
  • *SLE activity: increase in prednisone dose >10 mg/day or new requirement for intravenous steroids.

  • †Medications included if they were given for duration of pregnancy; steroids included for indication SLE treatment; dexamethasone given for indication of congenital heart block was not included, although two patients with SLE received it for this indication.

  • ‡Not routinely performed in patients with non-rheumatic disease.

  • §Normal versus pre-eclampsia; normal versus SLE+pre-eclampsia (p=0.0015and 0.0137), respectively.

  • ¶Normal versus pre-eclampsia; normal versus SLE; normal versus SLE+pre-eclampsia (p=0.034, 0.0019, and 0.0105), respectively.

  • ANA, antinuclear antibody; APLAb, antiphospholipid antibodies; APS, antiphospholipid antibody syndrome; NA, not applicable; ROM, rupture of membranes; SLE, systemic lupus erythematosus; SQ, subcutaneous.