Evidence map›Paper›PMID 41425214›Full record

ArticleFrontiers in sleep2025

Performance evaluation of a novel screening tool for depressive episodes in COMISA: a comparative analysis with standard neuropsychometric assessments.

Archie Defillo, Massimiliano Grassi, Silvia Daccò, Jennifer L Martin, Daniela Caldirola, Giampaolo Perna

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Article in Frontiers in sleep, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Archie DefilloClinical Research and Development Department, Medibio Limited, Savage, MN, United States.
Massimiliano GrassiClinical Research and Development Department, Medibio Limited, Savage, MN, United States.
Silvia DaccòClinical Research and Development Department, Medibio Limited, Savage, MN, United States.
Jennifer L MartinVA Greater Los Angeles Healthcare System, University of California, Los Angeles, Los Angeles, CA, United States.
Daniela CaldirolaDepartment of Biomedical Sciences, Humanitas University, Milan, Italy.
Giampaolo PernaDepartment of Biomedical Sciences, Humanitas University, Milan, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Insomnia and obstructive sleep apnea (OSA) are each linked to elevated risks of depression. When comorbid (COMISA), these risks increase further, highlighting the need for effective depression screening. This study evaluated the screening accuracy of a novel software, MEB-001, for detecting current major depressive episode (cMDE) in individuals identified as with and without suspected COMISA (sCOMISA). Methods: We conducted a retrospective sub-analysis from a prospective multicenter study at U.S. sleep clinics, including 296 adults who underwent routine polysomnography (PSG). Electrocardiogram and electroencephalogram signals, along with items 1 and 2 of the self-report depression screener Patient Health Questionnaire, 9 items (PHQ-9), were used to generate MEB-001 screening output. The Mini International Neuropsychiatric Interview (MINI) served as the diagnostic reference for cMDE. Sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) were calculated for MEB-001 and PHQ-9 (cut-off ≥10), with subgroup comparisons conducted using Fisher's exact and McNemar's tests ( Results: MINI identified cMDE in 15.5% of participants (16.9% in sCOMISA; 14.2% in non-COMISA). Against the MINI, MEB-001 achieved 84.8% sensitivity, 72.0% specificity, 35.8% PPV, and 96.3% NPV in the full cohort; PHQ-9 ≥10 showed similar performance (89.1, 68.4, 34.2, and 97.2%, respectively). MEB-01's performance did not differ between sCOMISA and non-sCOMISA (all Discussion: MEB-001 demonstrated consistent cMDE screening performance comparable to the PHQ-9, supporting its potential utility in sleep clinic settings.

Indexed as

comorbid insomnia and sleep apnea (COMISA)current major depressive episode (cMDE)depressioninsomniamini-international neuropsychiatric interviewobstructive sleep apnea (OSA)patient health questionnaire-9 (PHQ-9)

Identifiers

PMID41425214
PMCPMC12713888

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.