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Abstract Details

Migraine and Adverse Pregnancy Outcomes: the nuMoM2b Study
Headache
P5 - Poster Session 5 (11:45 AM-12:45 PM)
15-006

To quantify the associations between self-reported migraine and adverse pregnancy outcomes (APOs).

Migraine affects up to 3 in 10 women of childbearing age and is associated with endothelial dysfunction and inflammation.  Migraine history has previously been associated with APOs, including hypertensive disorders of pregnancy (HDP), preterm delivery, and low birth weight. Few prospective studies have investigated this association in a diverse US cohort.

The Nulliparous Pregnancy Outcomes Study Monitoring Mothers-to-be (nuMoM2b) study enrolled 10,038 US participants with singleton gestation in early pregnancy and followed them through delivery. History of migraine was self-reported. We defined APO as 1 or more of the following: gestational hypertension, preeclampsia/eclampsia, preterm delivery, fetal growth restriction, or stillbirth. We calculated odds ratios (OR) and 95% confidence intervals (95%CI) for the association of migraine with APO, adjusting for age, self-reported race/ethnicity, smoking history, chronic hypertension, obesity, chronic kidney disease, pre-gestational diabetes and autoimmune disorders. In secondary analyses, we calculated associations between migraine and individual APOs.

Of the 9169 participants included in the analysis, 1,752 (19.1%) reported migraine at the first study visit. Age and BMI did not differ between migraineurs and non-migraineurs. Migraineurs had higher proportions of self-identified White race, smoking, autoimmune and chronic kidney disease. After adjustment, migraineurs had increased odds of any APO (adjusted OR 1.28, 95% CI 1.13, 1.45). For individual APOs, migraineurs had higher odds of HDP (adjusted OR 1.18, 95% CI 1.05, 1.34) and preterm delivery (adjusted OR 1.41, 95% CI 1.15, 1.72), but not fetal growth restriction or stillbirth.

 

In this prospective cohort study in a large, diverse US population, migraine was independently associated with increased odds of APO. Migraine is an under-recognized risk factor for APO, especially HDP and preterm delivery, and patients who report migraine history may warrant closer monitoring during pregnancy.

Authors/Disclosures
Gular Mammadli, MD (Columbia University Irving Medical Center)
PRESENTER
Dr. Mammadli has nothing to disclose.
Eliza C. Miller, MD (University of Pittsburgh) Dr. Miller has received personal compensation in the range of $10,000-$49,999 for serving as an Expert Witness for medical malpractice cases. The institution of Dr. Miller has received research support from National Institutes of Health. Dr. Miller has a non-compensated relationship as a member of ASA Advisory Council with American Heart Association/American Stroke Association that is relevant to AAN interests or activities.
Sarah E. Vollbracht, MD (New York-Presbyterian Queens/Weill Cornell) Dr. Vollbracht has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Biohaven Pharmaceuticals. Dr. Vollbracht has received personal compensation in the range of $500-$4,999 for serving on a Speakers Bureau for Allergan.
No disclosure on file
No disclosure on file
No disclosure on file
Marianna S. Yugrakh, MD (Columbia University) The institution of Dr. Yugrakh has received research support from Teva.
No disclosure on file
No disclosure on file
No disclosure on file
Natalie Bello (Cedars-Sinai Medical Center) Natalie Bello has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for CRF. The institution of Natalie Bello has received research support from NIH.
No disclosure on file
No disclosure on file
No disclosure on file