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. 2024 Oct 23;11(6):e200328. doi: 10.1212/NXI.0000000000200328

Table.

Cohort Characteristics of Pregnancies Resulting in Live Births

Preconception DMT
OCR (n = 73) RTX (n = 24) NAT (n = 419) NAT-A (n = 82)a NAT-C (n = 82)a DMF (n = 164) Low (n = 1,329) p b
Pregnancy duration, median (IQR), weeks 39.0 (38.0–40.0) 38.1 (36.7–38.8) 38.7 (36.7–40.0) 38.9 (37.6–39.8) 38.0 (35.5–39.1) 39.0 (37.6–40.0) 39.0 (37.3–40.0) 0.052
Age at start of pregnancy, median (IQR), y 33.8 (30.7–37.3) 33.3 (29.1–35.0) 31.5 (28.6–34.4) 32.5 (28.5–35.3) 31.9 (29.4–34.0) 31.4 (28.4–34.2) 31.5 (28.2–34.6) 0.005
Time from first symptoms to start of pregnancy, median (IQR), y 7.10 (3.90–10.5) 6.16 (4.24–9.96) 7.41 (4.21–11.7) 7.59 (4.01–11.9) 8.59 (5.27–12.6) 5.70 (2.96–9.18) 5.83 (3.25–9.51) <0.001
DMT used before, median (IQR), n 1 (0,2) 1 (0,2) 1 (1,2) 1 (0,2) 2 (1,2) 1 (0,2) 0 (0,1) <0.001
EDSS score at start of pregnancy, n (%)c <0.001
 <2 25 (34.2) 12 (50) 198 (47.3) 39 (47.6) 41 (50.0) 95 (57.9) 674 (50.8)
 ≥2 28 (38.4) 7 (29.2) 122 (29.1) 21 (25.6) 24 (29.3) 28 (17.1) 213 (16.0)
 Missing 20 (27.4) 5 (20.8) 99 (23.6) 22 (26.8) 17 (20.7) 41 (25.0) 441 (33.2)
EDSS score at start of pregnancy, median (IQR)c 2 (1,2.5) 1.5 (0.5–2) 1.5 (1,2) 1 (0,2) 1.5 (1,2) 1 (1,1.5) 1 (0,1.5) <0.001
Range 0,5 0,6 0,6 0,3 0,6 0,6 0,6.5
ARR in 1 y before pregnancy, mean (SD) 0.14 (0.53) 0.13 (0.45) 0.11 (0.48) 0.05 (0.25) 0.11 (0.38) 0.20 (1.06) 0.24 (0.72) <0.001
DMT prepregnancy duration, median (IQR), mo 9.95 (5.82–18.1) 16.7 (9.27–24.8) 18.1 (9.10–32.0) 24.8 (9.91–38.2) 16.0 (6.22–30.4) 14.1 (8.07–24.8) 23.5 (10.7–44.8) <0.001
DMT washout, median (IQR), mo 1.87 (0–4.76) 3.43 (0.74–5.03)d 0 (0–0) 0 (0–1.32) 0 (0–0.821) <0.001
DMT duration into pregnancy, median (IQR), mo 0 (0–0.460) 0 (0–0)d 0.89 (0–6.42) 0.21 (0–1.13) 0.49 (0–1.35) <0.001
DMT initiated after delivery, n (%)e
 Ocrelizumab 43 (58.9) 1 (4.2) 12 (2.9) 0 0 2 (1.2) 1 (0.1)
 Natalizumab 2 (2.7) 0 304 (72.6) 82 (100) 82 (100) 6 (3.7) 18 (1.4)
 Dimethyl fumarate 0 0 3 (0.7) 0 0 76 (46.3) 25 (1.9)
 Lowf 1 (1.4) 1 (4.2) 9 (2.1) 0 0 9 (5.5) 719 (54.1)
 Sphingosine-1-phosphate modulatorg 1 (1.4) 0 14 (3.3) 0 0 4 (2.4) 38 (2.9)
 Rituximab 0 18 (75) 2 (0.5) 0 0 0 1 (0.1)
 Ofatumumab 2 (2.7) 1 (4.2) 1 (0.2) 0 0 1 (0.6) 0
 Alemtuzumab 0 0 9 (2.1) 0 0 0 1 (0.1)
 Cladribine 0 0 3 (0.7) 0 0 0 1 (0.1)
 None 24 (32.9) 3 (12.5) 62 (14.8) 0 0 66 (40.2) 525 (39.5)
Time to DMT initiation after delivery, median (IQR), moh 1.41 (0.49–3.02) 1.63 (0.77–1.91)d 0.89 (0.10–2.30) 2.25 (0.49–4.39) 2.43 (0.44–5.03) <0.001

Abbreviations: ARR = annualized relapse rate; DMF = dimethyl fumarate; DMT = disease-modifying therapy; EDSS = Expanded Disability Status Scale; IQR = interquartile range; NAT = natalizumab; OCR = ocrelizumab, RTX = rituximab.

a

NAT-A (active natalizumab strategy of continuation to ≥28 weeks of gestation and reinitiation within 1 month after delivery) and NAT-C (conservative strategy of cessation ≤4 weeks of gestation and reinitiation more than 1 month after delivery) were subset from the overall natalizumab (NAT) cohort.

b

Comparisons were between OCR, RTX, NAT, DMF, and low-efficacy DMT groups.

c

Calculated from women with available EDSS scores closest to start of pregnancy (within 1 year).

d

Data available for 16 of 24 women in the RTX cohort.

e

In the 6-mo postpartum period.

f

Low-efficacy DMT initiated in the postpartum period include interferon-beta, glatiramer acetate, teriflunomide, azathioprine, and mycophenolate.

g

Sphingosine-1-phosphate modulators include fingolimod and siponimod.

h

Women who initiated either preconception DMT or other DMTs.