Favaro Angela, Tenconi Elena, Santonastaso Paolo
Department of Neurosciences, University of Padua, Padua, Italy.
Arch Gen Psychiatry. 2006 Jan;63(1):82-8. doi: 10.1001/archpsyc.63.1.82.
Few prospective studies to date have investigated the role of obstetric complications in anorexia nervosa, and no study to our knowledge exists for this in bulimia nervosa.
To explore the role of obstetric complications in the development of eating disorders.
A blind analysis of the obstetric records of a sample of subjects with anorexia nervosa, with bulimia nervosa, and normal subjects was performed. All of the subjects included in the study belong to the same population birth cohort and were born in the 2 obstetric wards of Padua Hospital, Padua, Italy, between January 17, 1971, and December 30, 1979.
Part of the sample of subjects with eating disorders and all of the controls took part in a prevalence study carried out in 2 randomly selected areas of Padua. In addition, all of the subjects with anorexia nervosa and bulimia nervosa of the same birth cohort who were referred to an outpatient specialist unit were included. The final sample comprised 114 subjects with anorexia nervosa, 73 with bulimia nervosa, and 554 control subjects.
Several complications, such as maternal anemia (P = .03), diabetes mellitus (P = .04), preeclampsia (P = .02), placental infarction (P = .001), neonatal cardiac problems (P = .007), and hyporeactivity (P = .03), were significant independent predictors of the development of anorexia nervosa. The risk of developing anorexia nervosa increased with the total number of obstetric complications. In addition, an increasing number of complications significantly anticipated the age at onset of anorexia nervosa (P = .03). The obstetric complications significantly associated with bulimia nervosa were the following: placental infarction (P = .10), neonatal hyporeactivity (P = .005), early eating difficulties (P = .02), and a low birth weight for gestational age (P = .009). Being shorter for gestational age significantly differentiated subjects with bulimia nervosa from both those with anorexia nervosa (P = .04) and control subjects (P = .05).
A significantly higher risk of eating disorders was found for subjects with specific types of obstetric complications. An impairment in neurodevelopment could be implicated in the pathogenesis of eating disorders.
迄今为止,很少有前瞻性研究调查产科并发症在神经性厌食症中的作用,据我们所知,尚无关于神经性贪食症的此类研究。
探讨产科并发症在饮食失调发展中的作用。
对一组神经性厌食症患者、神经性贪食症患者和正常受试者的产科记录进行盲法分析。研究纳入的所有受试者均来自同一出生队列人群,于1971年1月17日至1979年12月30日在意大利帕多瓦市帕多瓦医院的两个产科病房出生。
部分饮食失调患者样本和所有对照参与了在帕多瓦市随机选择的两个区域进行的患病率研究。此外,还纳入了同一出生队列中所有转诊至门诊专科单位的神经性厌食症和神经性贪食症患者。最终样本包括114例神经性厌食症患者、73例神经性贪食症患者和554例对照受试者。
几种并发症,如母亲贫血(P = 0.03)、糖尿病(P = 0.04)、先兆子痫(P = 0.02)、胎盘梗死(P = 0.001)、新生儿心脏问题(P = 0.007)和反应低下(P = 0.03),是神经性厌食症发展的显著独立预测因素。神经性厌食症的发病风险随产科并发症总数的增加而增加。此外,并发症数量的增加显著预示了神经性厌食症的发病年龄(P = 0.03)。与神经性贪食症显著相关的产科并发症如下:胎盘梗死(P = 0.10)、新生儿反应低下(P = 0.005)、早期进食困难(P = 0.02)和小于胎龄儿(P = 0.009)。小于胎龄在区分神经性贪食症患者与神经性厌食症患者(P = 0.04)和对照受试者(P = 0.05)方面具有显著差异。
发现患有特定类型产科并发症的受试者患饮食失调的风险显著更高。神经发育受损可能与饮食失调的发病机制有关。