Evidence map›Paper›PMID 35562013›Full record

ReviewBrain research bulletin2022

Subcortical control of the default mode network: Role of the basal forebrain and implications for neuropsychiatric disorders.

David D Aguilar, James M McNally

Open access · hybridAbstract readReview
In one paragraph

Review in Brain research bulletin, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 7% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
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  8. Combined Dysfunction of the Amygdala and Nucleus Basalis Underlies Visual Hallucinations in Parkinson's Disease.Movement disorders : official journal of the Movement Disorder Society · 2025
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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

2 authors at 1 institution in 1 country.

David D AguilarVA Boston Healthcare System, West Roxbury, MA, USA; Department of Psychiatry, Harvard Medical School, Boston, MA, USA. Electronic address: David_Aguilar@hms.harvard.edu.
James M McNallyVA Boston Healthcare System, West Roxbury, MA, USA; Department of Psychiatry, Harvard Medical School, Boston, MA, USA. Electronic address: James_McNally@hms.harvard.edu.
Harvard University · US

Funding

Subcortical influence on the respiratory coordination of cortical neurodynamicsrelated to cognitionR21MH125242 · NIMH · HARVARD MEDICAL SCHOOL · PI MCKENNA, JAMES TIMOTHY, MCNALLY, JAMES M · 2021 to 2022
$363k
Tuning cortical E/I balance for translational modeling of psychiatric disordersI01BX004500 · VA · VA BOSTON HEALTH CARE SYSTEM · PI JAMES M MCNALLY · 2019 to 2026
–
BLRD VA I01 BX004500NIMH NIH HHS R21 MH125242
6 · The paper itself

Abstract

The precise interplay between large-scale functional neural systems throughout the brain is essential for performance of cognitive processes. In this review we focus on the default mode network (DMN), one such functional network that is active during periods of quiet wakefulness and believed to be involved in introspection and planning. Abnormalities in DMN functional connectivity and activation appear across many neuropsychiatric disorders, including schizophrenia. Recent evidence suggests subcortical regions including the basal forebrain are functionally and structurally important for regulation of DMN activity. Within the basal forebrain, subregions like the ventral pallidum may influence DMN activity and the nucleus basalis of Meynert can inhibit switching between brain networks. Interactions between DMN and other functional networks including the medial frontoparietal network (default), lateral frontoparietal network (control), midcingulo-insular network (salience), and dorsal frontoparietal network (attention) are also discussed in the context of neuropsychiatric disorders. Several subtypes of basal forebrain neurons have been identified including basal forebrain parvalbumin-containing or somatostatin-containing neurons which can regulate cortical gamma band oscillations and DMN-like behaviors, and basal forebrain cholinergic neurons which might gate access to sensory information during reinforcement learning. In this review, we explore this evidence, discuss the clinical implications on neuropsychiatric disorders, and compare neuroanatomy in the human vs rodent DMN. Finally, we address technological advancements which could help provide a more complete understanding of modulation of DMN function and describe newly identified BF therapeutic targets that could potentially help restore DMN-associated functional deficits in patients with a variety of neuropsychiatric disorders.

Indexed as

Basal ForebrainSchizophreniaBrainBrain MappingDefault Mode NetworkHumansMagnetic Resonance ImagingNerve NetParvalbuminsWakefulnessParvalbuminsBrain networksCholinergic neuronsFunctional magnetic resonance imagingMedial frontoparietal networkParvalbuminSchizophrenia

Identifiers

PMID35562013
PMCPMC9290753
OpenAlexW4280530526

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.