Evidence map›Paper›PMID 36459376›Full record

ArticleBehavior research methods2023

A new approach to diagnosing and researching developmental prosopagnosia: Excluded cases are impaired too.

Edwin J Burns, Elizabeth Gaunt, Betiel Kidane, Lucy Hunter, Jaylea Pulford

Open access · hybridAbstract read
In one paragraph

Article in Behavior research methods, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
5.2field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

20 citing papers in PubMed, 45 citations in OpenAlex.

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  8. Face naming and recollection represent key memory deficits in developmental prosopagnosia.Cortex; a journal devoted to the study of the nervous system and behavior · 2024
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  9. Poor face recognition predicts social anxiety in autism: A short report.Autism : the international journal of research and practice · 2024
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  13. Measure twice, cut once: Moving toward more inclusive, principled criteria for diagnosing developmental prosopagnosia.Cortex; a journal devoted to the study of the nervous system and behavior · 2024
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  14. Perceptual heterogeneity in developmental prosopagnosia is continuous, not categorical.Cortex; a journal devoted to the study of the nervous system and behavior · 2024
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  19. What is the prevalence of developmental prosopagnosia? An empirical assessment of different diagnostic cutoffs.Cortex; a journal devoted to the study of the nervous system and behavior · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Edwin J BurnsDepartment of Psychology, Edge Hill University, Ormskirk, UK. edwinjamesburns@gmail.com.ORCID 0000-0002-5938-5457
Elizabeth GauntDepartment of Psychology, Edge Hill University, Ormskirk, UK.
Betiel KidaneDepartment of Psychology, Edge Hill University, Ormskirk, UK.
Lucy HunterDepartment of Psychology, Edge Hill University, Ormskirk, UK.
Jaylea PulfordDepartment of Psychology, Edge Hill University, Ormskirk, UK.
Edge Hill University · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Developmental prosopagnosia is characterized by severe, lifelong difficulties when recognizing facial identity. Unfortunately, the most common diagnostic assessment (Cambridge Face Memory Test) misses 50-65% of individuals who believe that they have this condition. This results in such excluded cases' absence from scientific knowledge, effect sizes of impairment potentially overestimated, treatment efficacy underrated, and may elicit in them a negative experience of research. To estimate their symptomology and group-level impairments in face processing, we recruited a large cohort who believes that they have prosopagnosia. Matching prior reports, 56% did not meet criteria on the Cambridge Face Memory Test. However, the severity of their prosopagnosia symptoms and holistic perception deficits were comparable to those who did meet criteria. Excluded cases also exhibited face perception and memory impairments that were roughly one standard deviation below neurotypical norms, indicating the presence of objective problems. As the prosopagnosia index correctly classified virtually every case, we propose it should be the primary method for providing a diagnosis, prior to subtype categorization. We present researchers with a plan on how they can analyze these excluded prosopagnosia cases in their future work without negatively impacting their traditional findings. We anticipate such inclusion will enhance scientific knowledge, more accurately estimate effect sizes of impairments and treatments, and identify commonalities and distinctions between these different forms of prosopagnosia. Owing to their atypicalities in visual perception, we recommend that the prosopagnosia index should be used to screen out potential prosopagnosia cases from broader vision research.

Indexed as

Facial RecognitionProsopagnosiaHumansPattern Recognition, VisualRecognition, PsychologyVisual PerceptionApperceptiveAssociativeCriteriaDiagnosingProsopagnosiaProsopamnesiaSingle-case analysis

Identifiers

PMID36459376
PMCPMC9718472
OpenAlexW4310781802

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.