Gastroenterology
Volume 129, Issue 2 , Pages 454-463, August 2005

Celiac Disease and Risk of Adverse Fetal Outcome: A Population-Based Cohort Study

  • Jonas F. Ludvigsson

      Affiliations

    • Pediatric Department, Örebro University Hospital, Örebro, Sweden
    • Clinical Epidemiology Unit, Department of Medicine, Karolinska University Hospital, Karolinska Institute, Stockholm, Sweden
    • Corresponding Author InformationAddress requests for reprints to: Jonas F. Ludvigsson, Pediatric Dept, Örebro University Hospital, Örebro 70185, Sweden.fax: (46) 19-187915.
  • ,
  • Scott M. Montgomery

      Affiliations

    • Clinical Epidemiology Unit, Department of Medicine, Karolinska University Hospital, Karolinska Institute, Stockholm, Sweden
    • Clinical Research Center, Örebro University Hospital, Linkoping, Sweden
  • ,
  • Anders Ekbom

      Affiliations

    • Clinical Epidemiology Unit, Department of Medicine, Karolinska University Hospital, Karolinska Institute, Stockholm, Sweden
    • Harvard Medical School, Boston, Massachusetts

Received 27 January 2005; accepted 4 May 2005.

Background & Aims: Studies of maternal celiac disease (CD) and fetal outcome are inconsistent, and low statistical power is likely to have contributed to this inconsistency. We investigated the risk of adverse outcomes in women with CD diagnosed prior to pregnancy and in women who did not receive a diagnosis of CD until after the delivery. Methods: A national register-based cohort study restricted to women aged 15–44 years with singleton live born infants was used. We identified 2078 offspring to women who had received a diagnosis of CD (1964–2001): 1149 offspring to women diagnosed prior to birth and 929 offspring to women diagnosed after infant birth. Main outcome measures were: intrauterine growth retardation, low birth weight (<2500 g), very low birth weight (<1500 g), preterm birth (<37 gestational weeks), very preterm birth (<30 gestational weeks), and caesarean section. Results: Undiagnosed CD was associated with an increased risk of intrauterine growth retardation (OR = 1.62; 95% CI: 1.22–2.15), low birth weight (OR = 2.13; 95% CI: 1.66–2.75), very low birth weight (OR = 2.45; 95% CI: 1.35–4.43), preterm birth (OR = 1.71; 95% CI: 1.35–2.17), and caesarean section (OR = 1.82; 95% CI: 1.27–2.60). In contrast, a diagnosis of CD made before the birth was not associated with these adverse fetal outcomes. Conclusions: Undiagnosed maternal CD is a risk factor for unfavorable fetal outcomes, but the risks are reduced when CD has been diagnosed. CD diagnosed prior to pregnancy does not constitute a great a risk as undiagnosed CD.

Abbreviations used in this paper:  AOR, adjusted odds ratio, CD, celiac disease, IUGR, intrauterine growth retardation, LBW, low birth weight, VLBW, very low birth weight

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 Supported by grants from The Örebro Society of Medicine, The Sven Jerring Foundation, Karolinska Institute funds, The Swedish Society of Medicine, the Swedish Research Council, the Majblomman Foundation, and Örebro University Hospital (to J.F.L. [for manuscript preparation]).

PII: S0016-5085(05)01100-5

doi:10.1053/j.gastro.2005.05.065

Gastroenterology
Volume 129, Issue 2 , Pages 454-463, August 2005