Related Experiment Video
Updated: Jun 30, 2025

Design and Implementation of an fMRI Study Examining Thought Suppression in Young Women with, and At-risk, for Depression
Published on: May 19, 2015
Early childhood-onset rumination syndrome is clinically distinct from adolescent-onset rumination syndrome
Dennis M Yang1,2, Julia Sabella1,2, Ashley Kroon Van Diest3
1Department of Pediatrics, Division of Gastroenterology, Hepatology, and Nutrition, Nationwide Children's Hospital, Columbus, Ohio, USA.
Insights
Early-onset rumination syndrome (RS) in children presents differently than adolescent-onset RS, with distinct sex distributions and comorbidities. Early-onset RS shows a different clinical course and may have a unique pathogenesis.
Area of Science:
- Pediatric Gastroenterology
- Child Psychology
- Clinical Epidemiology
Background:
- Rumination syndrome (RS) in early childhood is understudied and difficult to manage.
- Understanding the differences between early-onset (EO) and adolescent-onset (AO) RS is crucial for effective treatment.
- This study aims to delineate the distinct characteristics and outcomes of these two patient groups.
Purpose of the Study:
- To compare the clinical characteristics, severity, and treatment outcomes of early-onset (EO) versus adolescent-onset (AO) rumination syndrome (RS) in children.
- To identify potential differences in pathogenesis and natural history between EO and AO RS.
Main Methods:
- An ambidirectional cohort study was conducted.
- Patients were categorized into EO (symptom onset ≤5 years, diagnosis ≤12 years) and AO (onset >12 years) groups.
- Demographics, clinical features, severity indicators, and outcomes were compared between the two groups.
Main Results:
- 49 EO and 52 AO RS patients were analyzed.
- EO RS showed a male predominance, while AO RS was predominantly female (p=0.016).
- EO patients had higher rates of developmental delay (24% vs. 8%) and lower rates of depression (0% vs. 23%) and anxiety (14% vs. 40%) compared to AO patients.
- EO RS presented with greater regurgitation frequency but lower vomiting frequency, leading to less meal skipping, reduced need for tube feeding, and less weight loss compared to AO RS.
- EO RS symptoms significantly improved over time, with reduced regurgitation and vomiting frequencies at follow-up.
Conclusions:
- Early-onset rumination syndrome is clinically distinct from adolescent-onset RS.
- Differences are observed in sex distribution, comorbid conditions (developmental delay, depression, anxiety), and initial presentation severity.
- The distinct clinical profiles suggest potentially different underlying pathogenesis and natural history for EO and AO RS.
Objectives:
Rumination syndrome (RS) beginning in early childhood or infancy is understudied and challenging to treat. Our objective is to compare the characteristics and outcomes of early-onset (EO) and adolescent-onset (AO) patients with RS.
Methods:
We conducted an ambidirectional cohort study of children diagnosed with RS at our institution. Patients were included in two groups: EO (RS symptom onset ≤5 years and diagnosis ≤12 years) and AO (onset >12 years). Patient characteristics, severity, and outcomes were compared between the groups.
Results:
We included 49 EO and 52 AO RS patients. The median ages of symptom onset and diagnosis in EO were 3.5 and 6 years, respectively; AO, 14.5 and 15 years. EO RS had a slight male predominance while AO was predominantly female (p = 0.016). EO patients were more likely to have developmental delay (24% vs. 8%, p = 0.029) and less likely to have depression (0% vs. 23%, p < 0.001) or anxiety (14% vs. 40%, p = 0.004). At baseline, EO RS was less severe than AO RS: EO RS had greater regurgitation frequency (p < 0.001) but lower vomiting frequency (p = 0.001), resulting in less meal skipping (p < 0.001), reliance on tube feeding or parenteral nutrition (p < 0.001), and weight loss (p = 0.035). EO RS symptoms improved over time: at follow-up, patients had lower regurgitation (p < 0.001) and vomiting frequency (p < 0.001) compared to baseline.
Conclusion:
EO RS is clinically distinct from AO RS, with differences in sex distribution, comorbid conditions, and severity of initial presentation. The pathogenesis and natural history of EO RS may be distinct from that of AO RS.
Related Concept Videos
Oppositional Defiant Disorder
Diagnostic Criteria and...
Revisionist Views of Adolescent and Adult Cognition
Cognitive Development During Adolescence
Autism Spectrum Disorder
These core symptoms manifest differently among individuals, ranging from mild to severe. The disorder's complexity extends beyond its clinical presentation, encompassing a diverse range of biological, cognitive, and sociocultural influences.
Depressive Disorders: MDD and Dysthymia
Piaget's Stage 4 of Cognitive Development
Abstract Reasoning and Hypothetical-Deductive Thinking
Unlike the concrete operational...

