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出生特征与生命历程中进食障碍的关联:来自瑞典 1975-1998 年出生的 200 万男性和女性的研究结果。

Associations between birth characteristics and eating disorders across the life course: findings from 2 million males and females born in Sweden, 1975-1998.

出版信息

Am J Epidemiol. 2014 Apr 1;179(7):852-63. doi: 10.1093/aje/kwt445. Epub 2014 Feb 18.

Abstract

Birth characteristics predict a range of major physical and mental disorders, but findings regarding eating disorders are inconsistent and inconclusive. This total-population Swedish cohort study identified 2,015,862 individuals born in 1975-1998 and followed them for anorexia nervosa, bulimia nervosa, and eating disorder not otherwise specified until the end of 2010. We examined associations with multiple family and birth characteristics and conducted within-family analyses to test for maternal-level confounding. In total, 1,019 males and 15,395 females received an eating disorder diagnosis. Anorexia nervosa was independently predicted by multiple birth (adjusted hazard ratio = 1.33, 95% confidence interval: 1.15, 1.53) for twins or triplets vs. singletons) and lower gestational age (adjusted hazard ratio = 0.96, 95% confidence interval: 0.95, 0.98) per extra week of gestation, with a clear dose-response pattern. Within-family analyses provided no evidence of residual maternal-level confounding. Higher birth weight for gestational age showed a strong, positive dose-response association with bulimia nervosa (adjusted hazard ratio = 1.15, 95% confidence interval: 1.09, 1.22, per each standard-deviation increase), again with no evidence of residual maternal-level confounding. We conclude that some perinatal characteristics may play causal, disease-specific roles in the development of eating disorders, including via perinatal variation within the normal range. Further research into the underlying mechanisms is warranted. Finally, several large population-based studies of anorexia nervosa have been conducted in twins; it is possible that these studies considerably overestimate prevalence.

摘要

出生特征可预测一系列主要的身心障碍,但有关饮食失调的发现结果不一致且没有定论。这项全人群瑞典队列研究纳入了 1975 年至 1998 年出生的 2015862 名个体,并对他们进行随访,直至 2010 年底,随访终点为神经性厌食症、神经性贪食症和未特定的饮食失调。我们研究了多种家庭和出生特征与这些疾病的相关性,并进行了基于家庭的分析,以检验母源性混杂的影响。共有 1019 名男性和 15395 名女性被诊断为饮食失调。与单胎妊娠相比,双胞胎或三胞胎(调整后的危险比=1.33,95%置信区间:1.15,1.53)以及每额外妊娠一周的胎龄(调整后的危险比=0.96,95%置信区间:0.95,0.98)与神经性厌食症的发生呈独立相关,且存在明确的剂量-反应关系。基于家庭的分析并未提供母源性混杂残留的证据。出生体重与胎龄比与神经性贪食症呈强烈的正剂量-反应关系(调整后的危险比=1.15,95%置信区间:1.09,1.22,每增加一个标准差),且同样不存在母源性混杂残留的证据。我们的结论是,一些围产期特征可能在饮食失调的发展中发挥特定病因的作用,包括在正常范围内的围产期变化。有必要对潜在的机制进行进一步研究。最后,几项针对神经性厌食症的大型双胞胎人群研究已经开展;这些研究可能大大高估了患病率。

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