Background Antroduodenal manometry (ADM) is the gold standard for diagnosing myopathy and neuropathy in patients with upper gastrointestinal (GI) disorders. However, ADM is invasive and costly. Body surface gastric mapping (BSGM) has emerged as a non-invasive test to assess gastric function. This study evaluates the correlation between BSGM and ADM in children. Methods Clinically indicated ADM was performed using high-resolution water-perfused motility catheters, with simultaneous BSGM. Real-time symptoms were tracked using a validated symptom logging app at 15-min intervals, and Nausea Severity Scale (NSS) scores recorded. Protocols involved a 2 hour fast, provocative testing, a meal, and over 1 hr of postprandial recordings. ADM tracings were categorized into neuropathy, myopathy, postprandial hypomotility, or normal. BSGM metrics included principal gastric frequency, BMI-adjusted amplitude, and Rhythm Index. Gastric emptying data were also evaluated. Results Fifteen subjects were recruited (13 female; ages 10-19 years, BMI 20.6+/-3.5 kg/m2). ADM results showed neuropathy (n=4), myopathy (n=1), post-prandial hypomotility (n=4), and normal motility (n=6). Patients with neuropathy had lower rhythm stability (0.16+/-0.03 vs 0.38+/-0.17; p=.001), accompanied by higher nausea scores (8.2+/-1.2 vs 3.15+/-2.9; p<.001) and bloating (7.3+/-0.9 vs 2.1+/-2.0; p<.001). ADM neuropathy correlated completely with dysrhythmia on BSGM. Normal ADM were consistent with normal BSGM in 83.3% of cases. Delayed gastric emptying did not correlate with a neuropathic diagnosis. Conclusion: Dysrhythmic BSGM phenotype reliably identified gastrointestinal neuropathy with identical results to ADM, with significant correlations to nausea and bloating severity. This study supports considering BSGM as an actionable biomarker when performing ADM is not feasible.
Competing Interest StatementG.O. and A.G. hold grants and intellectual property in Gastrointestinal Electrophysiology. G.O, A.G., S.C., and G.S. are shareholders and or employees of Alimetry. The remaining authors have no conflicts of interest to declare.
Funding StatementThe study did not receive any external funding
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The details of the IRB/oversight body that provided approval or exemption for the research described are given below:
The Children's Hospital of Philadelphia Institutional Review Board gave ethical approval for this work
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I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).
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Data AvailabilityAll data produced in the present study are available upon reasonable request to the authors
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