Munn-Chernoff Melissa A, Keel Pamela K, Klump Kelly L, Grant Julia D, Bucholz Kathleen K, Madden Pamela A F, Heath Andrew C, Duncan Alexis E
Department of Psychiatry and Midwest Alcoholism Research Center, Washington University School of Medicine, St. Louis, Missouri.
Department of Psychology, Florida State University, Tallahassee, Florida.
Int J Eat Disord. 2015 Sep;48(6):601-6. doi: 10.1002/eat.22378. Epub 2015 Mar 25.
Purging disorder (PD) was recently included as an otherwise specified feeding or eating disorder (OSFED) in the DSM-5; however, limited information is available on its prevalence, and its etiology is unknown.
Data from 1,790 monozygotic and 1,440 dizygotic European American female twins (age range = 18-29 years) from the Missouri Adolescent Female Twin Study were used to investigate prevalence and familial influences for PD. A structured clinical interview assessed lifetime DSM-IV criteria for eating disorders and PD. After adjustment for age, twin correlations and biometrical twin models were used to estimate familial (i.e., genetic plus shared environmental) influences on PD.
One hundred and twenty one (3.77%; 95% CI: 3.14, 4.49) women met criteria for lifetime PD. Twin correlations suggested that genetic, shared environmental, and nonshared environmental factors influenced liability to PD. Nonshared environmental factors accounted for 56% [35%, 79%] of the variance in PD. Although familial effects accounted for a significant proportion of variance (44% [21%, 65%]), it was not possible to disentangle the independent contributions of additive genetic effects (20% [0%, 65%]) and shared environmental effects (24% [0%, 57%]).
PD is a prevalent form of eating pathology. Familial factors are relevant to the development of PD but do not demonstrate the magnitude of heritable factors found for other eating disorders.
清除障碍(PD)最近在《精神疾病诊断与统计手册》第5版(DSM - 5)中被列为其他特定的喂养或进食障碍(OSFED);然而,关于其患病率的信息有限,且病因不明。
来自密苏里青少年女性双胞胎研究的1790对同卵和1440对异卵欧美女性双胞胎(年龄范围 = 18 - 29岁)的数据用于调查PD的患病率和家族影响。采用结构化临床访谈评估进食障碍和PD的终生DSM - IV标准。在对年龄进行调整后,使用双胞胎相关性和双生子模型来估计家族(即遗传加共享环境)对PD的影响。
121名(3.77%;95%置信区间:3.14,4.49)女性符合终生PD的标准。双胞胎相关性表明,遗传、共享环境和非共享环境因素影响了患PD的易感性。非共享环境因素占PD变异的56%[35%,79%]。虽然家族效应占变异的很大比例(44%[21%,65%]),但无法区分加性遗传效应(20%[0%,65%])和共享环境效应(24%[0%,57%])的独立贡献。
PD是一种常见的进食病理学形式。家族因素与PD的发展相关,但未显示出其他进食障碍中发现的遗传因素的程度。