4.7 Article

Influence of pregnancy on neuromyelitis optica spectrum disorder

期刊

NEUROLOGY
卷 78, 期 16, 页码 1264-1267

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/WNL.0b013e318250d812

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资金

  1. Korea Healthcare Technology RD Project
  2. Ministry for Health and Welfare, Republic of Korea [A080588-28]
  3. National Specialised Commissioning Group for NMO
  4. Bayer Schering Pharma
  5. Biogen Idec
  6. Mitsubishi Chemical Medience Corporation
  7. Ministry of Education, Science and Technology of Japan
  8. Eisai Inc.
  9. Mitsubishi Tanabe Pharma Corporation
  10. Astellas Pharma Inc.
  11. Takeda Pharmaceutical Company Limited
  12. Asahi Kasei Kuraray Medical Co., Ltd.
  13. Biogen Idec Japan
  14. Asahi Kasei Kuraray Medical Co.
  15. Ministry of Education, Science and Technology
  16. Ministry of Health, Labor and Welfare of Japan
  17. Merck Serono
  18. Novartis
  19. Teva
  20. Bayer Schering
  21. Ministry for Health, Welfare and Family Affairs
  22. Grants-in-Aid for Scientific Research [22229008] Funding Source: KAKEN

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Objective: To investigate the influence of pregnancy on patients with neuromyelitis optica spectrum disorder (NMOSD). Methods: A total of 190 women with NMOSD were enrolled from 7 referral hospitals in 4 countries. We reviewed medical records and used a structured questionnaire to investigate gravidity, parity, and the number of relapses during the 2 years before pregnancy, during each trimester of pregnancy, during the first and second trimesters after delivery, and for 6 months thereafter. The annualized relapse rate (ARR) was calculated for each period. Results: Of the 190 women with NMOSD, 40 patients experienced 54 informative pregnancies, and all of them were seropositive for aquaporin-4 antibody. Fourteen patients developed the first symptoms of NMOSD either during the pregnancy (3 patients) or within a year after delivery or abortion (8 and 3 patients, respectively). Twenty-six patients experienced 40 pregnancies after the onset of NMOSD (26 deliveries and 14 abortions [1 spontaneous and 13 elective]). There was one preterm delivery with birth defects and no stillbirths. The ARR during pregnancy did not differ from that before pregnancy, but it increased significantly during the first and second trimesters after delivery (5.3 and 3.7 times, respectively). Moreover, 77% of the deliveries were associated with postpartum relapses. Conclusion: The significantly increased relapse rate and numerous cases of NMOSD onset after pregnancy suggest that delivery adversely affects the course of NMOSD. Prospective studies are needed to confirm our findings. Neurology (R) 2012;78:1264-1267

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