Evidence map›Paper›PMID 38495781›Full record

ReviewAffective science2024

Why the Single-N Design Should Be the Default in Affective Neuroscience.

Håkan Fischer, Mats E Nilsson, Natalie C Ebner

Abstract readReview
In one paragraph

Review in Affective science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Article
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  4. Review
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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

3 authors.

Håkan FischerDepartment of Psychology, Stockholm University, 106 91 Stockholm, Sweden.ORCID 0000-0001-6710-1744
Mats E NilssonDepartment of Psychology, Stockholm University, 106 91 Stockholm, Sweden.
Natalie C EbnerDepartment of Psychology, University of Florida, Gainesville, FL 32611 USA.

Funding

Characterizing and Modulating Neurocognitive Processes of Learning to Trust and Distrust in Aging (Diversity Supplement)R01AG072658 · NIA · UNIVERSITY OF FLORIDA · PI Natalie C Ebner, Nichole Lighthall · 2022 to 2026
$3.6M
Uncovering and Surveilling Financial Deception Risk in Aging (Diversity Supplement to 1R01AG057764-01A1)R01AG057764 · NIA · UNIVERSITY OF FLORIDA · PI EBNER, NATALIE C, SPRENG, ROBERT NATHAN · 2018 to 2022
$2.5M
Mechanisms of Oxytocin's Analgesia in Older Adults (Diversity Supplement)R01AG059809 · NIA · UNIVERSITY OF FLORIDA · PI CRUZ-ALMEIDA, YENISEL, EBNER, NATALIE C · 2018 to 2022
$1.8M
The potential of oxytocin to reduce opioid abuse liability and pain among older adultsR21DA056813 · NIDA · UNIVERSITY OF FLORIDA · PI BERRY, MEREDITH, CRUZ-ALMEIDA, YENISEL · 2023 to 2024
$419k
NIA NIH HHS R01 AG057764NIA NIH HHS R01 AG059809NIA NIH HHS R01 AG072658NIDA NIH HHS R21 DA056813
6 · The paper itself

Abstract

Many studies in affective neuroscience rely on statistical procedures designed to estimate population averages and base their main conclusions on group averages. However, the obvious unit of analysis in affective neuroscience is the individual, not the group, because emotions are individual phenomena that typically vary across individuals. Conclusions based on group averages may therefore be misleading or wrong, if interpreted as statements about emotions of an individual, or meaningless, if interpreted as statements about the group, which has no emotions. We therefore advocate the Single-N design as the default strategy in research on emotions, testing one or several individuals extensively with the primary purpose of obtaining results at the individual level. In neuroscience, the equivalent to the Single-N design is deep imaging, the emerging trend of extensive measurements of activity in single brains. Apart from the fact that individuals react differently to emotional stimuli, they also vary in shape and size of their brains. Group-based analysis of brain imaging data therefore refers to an "average brain" that was activated in a way that may not be representative of the physiology of any of the tested individual brains, nor of how these brains responded to the experimental stimuli. Deep imaging avoids such group-averaging artifacts by simply focusing on the individual brain. This methodological shift toward individual analysis has already opened new research areas in fields like vision science. Inspired by this, we call for a corresponding shift in affective neuroscience, away from group averages, and toward experimental designs targeting the individual.

Indexed as

Brain imagingEmotionMethodsPsychophysics approach

Identifiers

PMID38495781
PMCPMC10942943

What OpenQuestion holds

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LicenceCC BY
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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.