Eating disorders (ED) are mental health disorders characterised by severe disturbances in eating behaviour that significantly impact an individual’s emotional, psychosocial and physical well-being (Bannatyne et al. 2018). Current diagnostic classifications of ED include anorexia nervosa (AN), bulimia nervosa (BN) and binge-eating disorder (BED) as full threshold ED. ED typically affect women of reproductive age (Easter et al. 2014).

Early childhood is a crucial time for the development of the mother–child relationship. It is during this time that children develop psychosocially, engage in social learning and express their temperament—which is a biological tendency within each child but it is shaped by complex interactions between genetic, biological and environmental factors (Shiner et al. 2012).

Risk for developmental problems in children of women with psychiatric disorder has been well documented in literature and several aspects of children’s development can be affected, including their physical, cognitive, social, emotional and behavioural development (Ramchandani and Stein 2003). Fewer studies are available regarding the impact of ED on child development.

However, the literature available suggests that children of mothers with ED have an increased risk for negative developmental outcomes, including cognitive, social and emotional disturbances (Patel et al. 2002). Research has shown that children of mothers with ED are more likely to develop an emotional disorder at the age of 7 and 10 (Micali et al. 2014a), they are more likely to show neurobehavioural dysregulation early after birth and poorer language and motor development at 1 year (Barona et al. 2017).

Furthermore, there is evidence that children of mothers with ED are more likely to develop ED themselves (Kothari et al. 2013).

Family and twin studies have consistently demonstrated that ED have a strong genetic component (Mazzeo et al. 2005); however, the environment is likely to play a crucial role in the expression of underlying genetic predispositions.

In 2005, Bulik et al. (2005) proposed a cycle of risk model for the development of AN, whereby the maternal effect of AN on their children via perinatal complications is hypothesised as being influenced by environmental factors, genetic factors and environmental factors that are highly influenced by maternal genotype (i.e. pregnancy nutrition, weight gain in utero, appearance focus and restrictive eating during childhood/adolescence). In 2009, Micali and Treasure suggested a risk model for the impact of maternal ED on child development that embraces all ED focusing on in utero mechanisms. In particular, the model explained the effect of a maternal ED in pregnancy on the foetus via nutritional factors (including protein deficiency, low folate and low iron intake) and comorbid psychopathology (i.e. comorbid anxiety and depression and in turn via increased glucocorticoids and corticotrophin-releasing hormone) which both could lead to obstetric complications (Micali and Treasure 2009). The influence of parental ED on child phenotype might likely be the result of a complex interplay between genetic (maternal and child) and environmental factors.

Understanding the mechanisms leading from maternal ED to adverse child development could help to determine both risk and protective factors that could be potentially targeted for intervention.

To date, only one recent systematic review has been published on this topic in the last several years and the authors did focus only on the most recent findings (2015 onwards) (Watson et al. 2018). Previous reviews focusing on children of mothers with ED include (Patel et al. 2002) and (Park et al. 2003). No systematic reviews have been carried out so far covering the period between 2003 and 2015 and many relevant population-based studies have been carried out over this period.

The purpose of our paper is to provide an overview of the impact of maternal ED on child development. Particularly, this review will focus on effects on developmental aspects, across the spectrum of feeding and eating behaviour, neuropsychological profile and cognitive development, psychopathology and temperament.

Methods and materials

Data source

A systematic and comprehensive search of databases, including PsychInfo, Embase and Medline, was carried out for studies published between January 1980 and September 2018. The search was performed using the following mesh terms and keywords: (‘maternal eating disorders’ or ‘maternal anorexia nervosa’ or ‘maternal bulimia nervosa’ or ‘maternal binge eating disorder’ or ‘mothers with eating disorders’ or ‘mothers with anorexia nervosa’ or ‘mothers with bulimia nervosa’ or ‘mothers with binge eating disorder’) and (‘child development’ or ‘child language development’ or ‘child feeding’ or ‘child cognitive development’ or ‘child temperament’ or ‘child psychopathology’).

Study selection

Inclusion criteria for the studies included (1) exposure (mothers) diagnosed with any ED (i.e. AN, BN and BED) either active or past, (2) the outcome was a measure of child development assessed from birth up until 12 years of age, (3) studies published in English and (4) primary studies.

Exclusion criteria for the studies included the following: studies were excluded if the aims were to investigate child eating pathology. Papers were also excluded if an intervention was assessed such as video-feedback interactional treatment.

Quality assessment and data extraction

Two authors (M.G.M. and M.B.) independently screened, extracted and cross-checked the data based on a priori exclusion and inclusion criteria. The quality of the final studies was also independently checked by both authors using the Newcastle–Ottawa Scale (NOS) for assessing the quality of non-randomised studies in meta-analyses (Table 1). The above scale includes case–control and cohort studies.

Table 1 Studies exploring the impact of maternal Eating Disorder (ED) on child development

For each study, the following data were extracted when available: demographic information, including participant characteristics (sample size ad mean age), ED type (AN, BN, BED), ED status (actual vs. recovered); measures used to certain exposure and outcome. The identified studies investigated a number of different child outcomes. After discussion between authors (M.B., M.G.M., N.M.), four domains were discussed: feeding/eating, neuropsychological profile/cognitive development, psychopathology and temperament. However, a range of studies investigated more than one outcome and were included in more than one domain (Table 1).


Search findings

A PRISMA flow diagram presents all phases of the review (Fig. 1) (Moher et al. 2009).

Fig. 1
figure 1

PRISMA flow diagram showing study selection process

Most studies used case–control (n = 17) and cohort design (n = 16) and one early study used an uncontrolled design. The majority of studies were published within the last decade (n = 25) with 59% published within the last 5 years (2013–2018).

Studies included measured various aspects of child development: feeding/eating (n = 17), cognitive development/neuropsychological profile (n = 6), psychopathology (n = 12) and infant temperament (n = 4). Five studies fit more than one domain.

Characteristics of the 34 articles included in the systematic review are shown in Table 1.

Quality assessment

The research design and content of studies was well executed with over 90% rated as strong. The four studies rated as moderate were due to (1) poor representativeness of cases, poorly defined controls and ascertainment of exposure; (2) lack of comparability of cases and controls on the basis of design or analysis (Blissett and Meyer 2006); (3) one study being uncontrolled (Hodes et al. 1997); and (4) no description of control group, no mention of history of outcome (Saltzman et al. 2016). It is worth noting that sample size was not accounted for as some studies rated as strong included small sample sizes of less than 10 (Evans and le Grange 1995). Therefore, a strong and positive overall assessment should be interpreted with caution.

Study results

Feeding outcomes (n = 17)

Given its relevance, the impact of maternal ED on children’s feeding and mealtimes is an area that has received considerable attention. Feeding the infant is a crucial task of parenting not only because it can absorb considerable part of the day in the early stages of life but also because it is one of the most important means of communication between mother and child (Silva et al. 2016).

Review of the present studies showed that mothers with ED might exhibit problems in feeding behaviours with their offspring starting from breast feeding. A number of population-based studies investigated the impact of ED on breast feeding, yielding discrepant findings (Micali et al. 2011, 2009). A large population-based study showed that women with a history of ED were more likely to start breast feeding and less likely to stop during the first year of the infant life. More specifically, mothers with BN were more likely to continue breast feeding and these differences persisted even after adjusting for confounding factors (Micali et al. 2009). A similar study found that women with ED started breast feeding their infants as often as controls; however, they were more likely to interrupt early (Torgersen et al. 2010). Conversely, Nguyen and colleagues found that mothers with a history of ED were slightly less likely to initiate breast feeding, although no longer significant after adjustment (socio-demographics, body mass index (BMI), maternal psychiatric symptoms) (Nguyen et al. 2017).

Although feeding difficulties are common in early stages of the infant’s life, mothers with AN reported increased feeding problems including exhaustion during feeding, slow feeding and no established feeding routine (Micali et al. 2011, 2009). On the other hand, infants of women with BN had higher levels of refusal to take solids in comparison to controls (Micali et al. 2009). Blisset and Meyer found similar results with some gender specificity, showing that maternal eating psychopathology predicted food refusal in girls but not boys. Symptoms of low maternal depression combined with high bulimic scores were significantly associated with food refusal in girls (Blissett and Meyer 2006). Conversely, Whelan and Cooper did not find the gender of the child to be related to maternal ED history, nor did it moderate the relationship between feeding difficulties and maternal ED (Whelan and Cooper 2000).

There is a well-known relationship between specific parenting styles in women with EDs and feeding problems in their offspring. An early study found that negative expressed emotions and more intrusive behaviours were more frequent among mothers with ED compared to controls during both mealtime and play (Stein et al. 1994). Mealtime interaction in offspring (ages 1–4) and mothers with ED compared to controls was also investigated by Waugh and Bulik (1999) who found that control mothers made more positive eating comments while mothers with ED tended to be more negative.

Differences between ED diagnoses and their impact on infant feeding problems are worth noting. Saltzman and colleagues found that maternal BED predicted use of more nonresponsive feeding practices (i.e. emotion regulation, restriction for health, pressure to eat and food as reward), indirectly through more distress responses to children’s negative emotions. Maternal BED was associated with greater use of distress responses, which indirectly predicted higher child BMI percentile through food as reward feeding practices (Saltzman et al. 2016). Also, mothers with BN or BED were more likely to report higher levels of restrictive feeding styles compared to controls (Reba-Harrelson et al. 2010), and mothers with a history of AN were more likely to use less pressuring feeding strategies compared to controls (de Barse et al. 2015).

Maternal ED can also influence nutritional intake, dietary patterns and diet quality in infants.

Easter and colleagues found that children of mothers with ED reported higher scores on the ‘health conscious/vegetarian’ dietary pattern (diet high in vegetarian foods, nuts, salad, rice, pasta and fruits) across all four time periods (ages 3, 4, 7 and 9) when compared with controls (Easter et al. 2013). Furthermore, they showed less adherence to the ‘traditional’ dietary pattern across all four time points. Energy intake was higher in the BN and AN + BN group, and this intake increased significantly over time for children of mothers with BN (Easter et al. 2013). In another study, Torgersen et al. (2015) found that mothers with BN and BED were less likely to use ‘homemade traditional food’ than ‘commercial jarred baby food’ when compared with mothers without ED; however, in women with BED, the associations were significant only before controlling for relevant confounders (Torgersen et al. 2015). Nguyen and colleagues found that children of mothers with life-time ED had higher diet quality at 1 year (Nguyen et al. 2017). Mothers with histories of ED may also be more likely to take ‘special approaches’ to feeding their children, such as limiting the amount of processed foods or eliminating other types or classes of foods (Hoffman et al. 2014).

Body image distortion, core symptoms of both AN and BN can also have an impact on feeding practices. In a recent study conducted by our team, we found that women with both past and current ED reported higher concerns about their infant being/becoming overweight compared with controls, respectively, at 8 weeks and 6 months and 6 months only postnatally. Also, women with past ED showed less awareness of infant hunger and satiety cues compared with HC at 8 weeks (Martini et al. 2018).

Cognitive development and neuropsychological profile (n = 6)

There is a growing evidence to suggest that ED are characterised by a specific neurocognitive profile including alterations in attention, visuospatial ability, memory, social cognition and executive functions, encompassing set shifting and central coherence (Giombini et al. 2018; Lang et al. 2014; Westwood et al. 2016). These profiles observed during active illness were thought to be a complex interplay between risk and protective factors, given the genetic profile and the drive to high educational achievement and perfectionism, common features of ED profile (Bardone-Cone et al. 2010). Also, these might be intermediate phenotypes, an early risk marker that are thought to lie between genetic/biological risk and actual phenotypical manifestations (Micali and Dahlgren 2016).

Research on neuropsychological profiles in children of women with ED aimed mainly at understanding both the impact of maternal ED on their children and to obtain a better understanding of intermediate endophenotypes of ED.

In the study carried out by Kothari et al. (2013), the investigation of neuropsychological profiles showed that children of mothers with AN had high full-scale and performance IQ, increased working memory (WM) capacity, better visuospatial functioning and decreased attentional control when compared to controls (Kothari et al. 2013). Another study investigating the early cognitive development (18 months and 4 years) in a sub-set of these children showed that children of women with lifetime AN had difficulties with social understanding, poorer motor skills, planning and abstract reasoning (Kothari et al. 2014). In a recent longitudinal study of children of mothers with ED, we recently found that infants of mothers with ED had poorer language and motor development compared to control mothers. Interestingly, after studying differential outcomes based on active versus past ED, we found that child cognitive difficulties were associated both with maternal active ED and past ED (Barona et al. 2017). Overall, these findings highlight early developmental difficulties in motor and cognitive development in offspring of ED mothers.

The study of later cognitive characteristics suggests a more specific pattern of strengths and difficulties across several domains of cognition, for example, higher IQ, better visuospatial performance and WM in children of mothers with lifetime AN, and poorer visuospatial functioning in children of mothers with lifetime BN (Barona et al. 2017).

Only one study to date has investigated social cognition in children of mothers with ED in mid-childhood and early adolescence, with some evidence of differences between at-risk offspring and controls. In particular, differential facial emotion processing, poorer recognition of fear, and higher scores on the social communication disorders checklist were present in children of mothers with binge eating and purging behaviours, the latter also present in children of mothers with lifetime BED (Kothari et al. 2015).

Finally, in a small longitudinal cohort study, Koubaa and colleagues found that children born to mothers with AN or BN had significantly higher Five to Fifteen (validated parent questionnaire assessing neurocognitive development) scores than controls reflecting difficulties in language and social skills (Koubaa et al. 2013).

Psychopathology (N = 12)

There is strong evidence that parental mental illness is associated with psychopathology in offspring, establishing that children of parents with psychiatric disorders are at higher risk of developing psychopathology themselves (Rasic et al. 2013). Research has also shown that familiar risk is only partly diagnosis-specific meaning that children might develop the same parental diagnosis (homotypic transmission) but may be also at risk for a range of other psychiatric disorders (heterotypic transmission) (Siegenthaler et al. 2012). However, the effect of maternal ED on their offspring psychopathology has received less attention.

Of the studies in this domain, five specifically investigated psychological/emotional development (Barbin et al. 2002; Cimino et al. 2016, 2013, 2015; Sadeh-Sharvit et al. 2016b) and seven explored general psychopathology (Barona et al. 2016; Cimino et al. 2018; Evans and le Grange 1995; Hodes et al. 1997; Micali et al. 2014a, 2014b; Reba-Harrelson et al. 2010).

A large longitudinal cohort study identified a higher risk for emotional and behavioural disorders in offspring of ED mothers at an early age (3.5 years). Specifically, the authors identified associations between maternal ED type (AN vs. BN) and child psychopathology (emotional vs. behavioural problems), as well as gender differences (Micali et al. 2014b). Emotional difficulties were found in both girls and boys of mothers with AN, while more hyperactivity and peer difficulties were found in both girls and boys of mothers with BN. This study also aimed to understand risk mechanisms and highlighted a mediating role for maternal anxiety and depression in the postpartum. These findings were confirmed and extended in a later study when the same children were aged 7, 10 and 13, where maternal EDs (both AN and BN) strongly predicted emotional and anxiety disorders (Micali et al. 2014a). A recent longitudinal study showed that maternal ED was associated with childhood psychopathology in girls and boys at age 7, both emotional and behavioural problems. Disorder and gender-specific findings across studies point to an effect of maternal lifetime AN on emotional disorders, in particular anxiety, across ages; while maternal BN seems to be associated with hyperactivity, conduct and peer problems (Barona et al. 2016).

These findings support those of case–control studies. In two longitudinal studies using the Child Behaviour Checklist (CBCL), the authors found that children of mothers with ED reported higher externalising and internalising scores from the CBCL compared to controls (Cimino et al. 2015, 2018). The emotional-adaptive profiles of children in the clinical group of mothers with ED scored significantly higher in all dimensions of the CBCL (Cimino et al. 2013). More specifically, externalising problems increased over time (Cimino et al. 2015).

The same authors carried out other two longitudinal studies aimed at investigating the emotional and behavioural profile of children of one or both parents with BED and adult–child feeding interaction (Cimino et al. 2016, 2018). They found that the children with one or both parents diagnosed with BED had higher scores on the internalising and externalising scales, and higher levels of emotional and behavioural difficulties (Cimino et al. 2016). Furthermore, children with both parents with BED showed the highest affective, anxiety, oppositional/defiant, and autism spectrum problems versus children of families with only one BED diagnosed father. Maternal BED was associated with children’s affective and autism spectrum problems, and diagnosis of BED in both parents had an effect on infants’ affective problems. Paternal BED had an effect on oppositional/defiant problems through the quality of father–infant interactions, and maternal BED had an effect on the offspring’s affective and anxiety problems through the mediation of mother–infant interactions (Cimino et al. 2018).

On the contrary, Barbin et al. did not find any difference in terms of psychological adjustment on both subscales of internalising and externalising in children of mothers with ED compared to healthy controls (Barbin et al. 2002).

In two early small studies, authors found that half of children of mothers with ED displayed psychiatric problems such hyperactivity, avoidant behaviour, enuresis, insecure attachment, depression, fears, personality problems, stuttering, violent temperament and oppositional defiant behaviour (Evans and le Grange 1995) and OCD (Hodes et al. 1997), respectively.

The latter association has also been found in a more recent large cohort study conducted by Reba-Harrelson and colleagues. The authors found that children of mothers with binge BED or BN were significantly more likely to exhibit symptoms of anxiety compared to children of control group mothers. Children of mothers with BN were also significantly more likely to exhibit obsessive-compulsive symptoms than children of non-eating-disordered mothers. All those with AN, BN or BED were significantly more likely to have children who exhibited symptoms of depression (Reba-Harrelson et al. 2010).

Likewise in a small recent study, mothers with ED reported higher levels of behavioural problems in their children compared to control mothers (Sadeh-Sharvit et al. 2016b).

Temperament (N = 4)

Temperament is defined as early appearing, biologically rooted, basic personality dimension (Bates et al. 1995). Although temperament is said to be a biological tendency within each child, environmental contexts, especially the social context, interrelate with the genetic tendencies of each child (Shiner et al. 2012).

Mothers with EDs have been shown to be more likely to describe their infant as having a difficult temperament. Compared to women with no history or current EDs, they tend to rate their children as having high levels of difficult temperament (Zerwas et al. 2012) and perceive them as having greater negative affect, that is, demonstrating more sadness, irritability and crying compared to controls (Agras et al. 1999). In a more recent large longitudinal study, we found that mothers with ED were more likely to perceive their children as having a ‘difficult temperament’ characterised by the child being less happy and active than other children their age, more restless and as having more tantrums and as being less cautious and guarded than other children their age (Barona et al. 2016). On the contrary in an early study, the authors did not observe any difference in childhood temperament between children born from ED mothers and controls (Waugh and Bulik 1999).


The literature regarding the impact of maternal ED on child development has expanded in the last decade. Albeit earlier studies focusing on small clinical samples, larger population-based samples have recently increased our knowledge on the topic.

Overall, the literature suggests that maternal ED impact on child cognitive, psychological and feeding and eating development.

Regarding feeding and eating, research shows that children of mothers with ED tend to experience more difficulties in feeding their children both in infancy and childhood. Although studies on breast feeding yield mixed results, women with ED often report difficulties with this. Throughout toddler years, difficulties such as slow feeding, small quantities feeding and not having established feeding routines emerged as common among ED mothers. Restricting parental feeding styles, negative expressed emotions and intrusive behaviours also appeared to be more frequent in ED mothers compared to controls. The most recent findings (Martini et al. 2018; Saltzman et al. 2016) are in line with earlier research (Stein et al. 1994). To date, it is not possible to disentangle the influence of genetic predisposition versus environmental factors, though likely both have a role. Future research investigating genotype–environment interface is warranted to provide further insight.

Although the current literature is less prominent, available findings shows that a maternal lifetime history of ED may have a negative impact also on children’s cognitive, psychological development and psychopathology.

Interestingly, recent studies have identified shared genetic risk between ED and other psychiatric disorders, i.e. schizophrenia and BED (Solmi et al. 2019) and AN and obsessive compulsive disorder (OCD) but also other positive genetic correlations between AN and schizophrenia and AN and neuroticism (Duncan et al. 2017; Yilmaz et al. 2018). These findings suggest that the genetic risk transmitted will impact on the behavioural, physiological and medical phenotypes expressed in children. Therefore, we might assume that children of AN women have a higher genetic risk of developing a wide range of phenotypes and psychiatric disorders such as psychosis, neuroticism, educational attainment but also lower BMI and lower risk of diabetes. Less is known on cognition and neuropsychological characteristics in offspring of ED mothers prior to the onset of psychopathology, and these might be an important focus of study in at-risk offspring, helping future prevention and early interventions.

Strengths and limitations

This systematic review has several strengths. First, it is the first systematic review summarising the existing findings from 1980 until 2018 on the impact of maternal ED on child development, and its findings can be valuable in deriving future hypothesis.

Second, the majority of studies relied on community-based or register-based samples rather than clinical samples; therefore, selection bias in the original studies is likely to be small.

Moreover, if an association between maternal ED and child development has been established in population-based studies, which are more likely to include less severe case of ED, our results are liable to be an underestimation of the effect.

However, some limitations should also have to be taken into account. Some of the studies reviewed above are single findings and need replication. Also, the vast majority of the studies explored mother–child dyad and did not involve the fathers. Although ED have a higher incidence in women than in men, gender ration is less skewed in BED than BN and AN (Hudson et al. 2007) and paternal ED can also have an impact on child development.

Studies showed a high degree of heterogeneity in the way the ED diagnosis is established, ranging from self-reported questionnaires (used in cohort studies such as ALSPAC (Easter et al. 2013; Micali et al. 2009, 2011, 2014a, 2014b, ), DNBC (Barona et al. 2016), Generation R study (de Barse et al. 2015; Nguyen et al. 2017), MoBa (Torgersen et al. 2015)) to structured interviews using both the Diagnostic and Statistical Manual (Agras et al. 1999; Cimino et al. 2016; Evans and le Grange 1995; Stein 1999; Waugh and Bulik 1999; Whelan and Cooper 2000) and SCID I (Barona et al. 2017; Cimino et al. 2015, 2018; Hoffman et al. 2014; Kothari et al. 2015; Martini et al. 2018).

It is important to point out that parental psychopathology does not always impact on child development in a negative way. This might be due to numerous factors including protective family network, child resilience, early access to mental health services, parenting abilities etc.

Future research should focus on the protective factors that moderate the relationship between maternal ED and adverse child outcomes leading to a healthy development of the child. This would shed light into mechanisms that could be potentially directed for intervention. For example, further research could introduce fathers and explore their roles in the family dynamics and in ameliorating, exacerbating or acting independently of the possible influence of a mother with ED.


In summary, maternal ED have an impact on child psychological, cognitive and eating development, and might affect the development of ED in the offspring. Despite this evidence, little is known on how genetic and environmental factors interplay and affect risk. As maternal psychopathology not always negatively affect child development, future research should focus on resilience and on which protective factors have impact on positive outcome. These factors can be then used as therapeutic and preventative targets.