Evidence map›Paper›PMID 32291962›Full record

ArticleAlzheimer's & dementia : the journal of the Alzheimer's Association2020

Neurovascular and immune mechanisms that regulate postoperative delirium superimposed on dementia.

Ping Wang, Ravikanth Velagapudi, Cuicui Kong, Ramona M Rodriguiz, William C Wetsel, Ting Yang, Miles Berger, Harris A Gelbard, Carol A Colton, Niccolò Terrando

Open access · hybridAbstract read
In one paragraph

Article in Alzheimer's & dementia : the journal of the Alzheimer's Association, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed, 1 pooled it
9.1field-weighted citation impact, top 2% 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

77 citing papers in PubMed, 1 synthesis or guideline pooled it, 119 citations in OpenAlex.

  1. Pooled it
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  8. Animal models of delirium: a narrative review.Translational psychiatry · 2026
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17 more citing papers are in PubMed but not listed here.

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

10 authors at 4 institutions in 1 country.

Ping WangDepartment of Anesthesiology, Duke University Medical Center, Durham, North Carolina, USA.
Ravikanth VelagapudiDepartment of Anesthesiology, Duke University Medical Center, Durham, North Carolina, USA.
Cuicui KongDepartment of Anesthesiology, Duke University Medical Center, Durham, North Carolina, USA.
Ramona M RodriguizDepartment of Psychiatry and Behavioral Sciences, Mouse Behavioral and Neuroendocrine Analysis Core Facility, Duke University Medical Center, Durham, North Carolina, USA.
William C WetselDepartment of Psychiatry and Behavioral Sciences, Mouse Behavioral and Neuroendocrine Analysis Core Facility, Duke University Medical Center, Durham, North Carolina, USA.
Ting YangDepartment of Medicine, Division of Nephrology, Duke University Medical Center, Durham, North Carolina, USA.
Miles BergerDepartment of Anesthesiology, Duke University Medical Center, Durham, North Carolina, USA.
Harris A GelbardCenter for Neurotherapeutics Discovery, University of Rochester Medical Center, Rochester, New York, USA.
Carol A ColtonDepartment of Neurology, Duke University Medical Center, Durham, North Carolina, USA.
Niccolò TerrandoDepartment of Anesthesiology, Duke University Medical Center, Durham, North Carolina, USA.
Duke University Hospital · USDuke Medical Center · USDuke University · USUniversity of Rochester Medical Center · US

Funding

Resource Core 3 - Metabolomics CoreP30AG028716 · NIA · DUKE UNIVERSITY · PI Sarah B. Peskoe · 2006 to 2026
$24.6M
Regional Biocontainment Laboratory (RBL)UC6AI058607 · NIAID · DUKE UNIVERSITY · PI WILLIAMS, R SANDERS · 2003 to 2005
$16.3M
Neurovascular dysfunction in delirium superimposed on dementiaR01AG057525 · NIA · DUKE UNIVERSITY · PI Niccolo Terrando · 2017 to 2026
$6.7M
Neuro-inflammation in Postoperative Cognitive Dysfunction: CSF and fMRI StudiesK76AG057022 · NIA · DUKE UNIVERSITY · PI BERGER, MILES · 2017 to 2022
$1.4M
Lightsheet Imaging SystemS10OD020010 · OD · DUKE UNIVERSITY · PI CAMERON, LISA A. · 2016 to 2016
$597k
Bioelectronic rescue of cognitive impairment after surgeryR21AG055877 · NIA · DUKE UNIVERSITY · PI TERRANDO, NICCOLO · 2018 to 2019
$436k
Targeting microbially-derived juvenile protective factors to resolve neuroinflammation and deliriumR03AG064260 · NIA · DUKE UNIVERSITY · PI TERRANDO, NICCOLO, WISCHMEYER, PAUL E · 2019 to 2020
$322k
NIAID NIH HHS UC6 AI058607NIA NIH HHS K76 AG057022NIA NIH HHS P30 AG028716NIA NIH HHS R01 AG057525NIA NIH HHS R03 AG064260NIA NIH HHS R21 AG055877NIH HHS S10 OD020010
6 · The paper itself

Abstract

objectiveThe present work evaluates the relationship between postoperative immune and neurovascular changes and the pathogenesis of surgery-induced delirium superimposed on dementia. BACKGROUND AND RATIONALE: Postoperative delirium is a common complication in many older adults and in patients with dementia including Alzheimer's disease (AD). The course of delirium can be particularly debilitating, while its pathophysiology remains poorly defined. HISTORICAL EVOLUTION: As of 2019, an estimated 5.8 million people of all ages have been diagnosed with AD, 97% of whom are >65 years of age. Each year, many of these patients require surgery. However, anesthesia and surgery can increase the risk for further cognitive decline. Surgery triggers neuroinflammation both in animal models and in humans, and a failure to resolve this inflammatory state may contribute to perioperative neurocognitive disorders as well as neurodegenerative pathology. UPDATED HYPOTHESIS: We propose an immunovascular hypothesis whereby dysregulated innate immunity negatively affects the blood-brain interface, which triggers delirium and thereby exacerbates AD neuropathology. EARLY EXPERIMENTAL DATA: We have developed a translational model to study delirium superimposed on dementia in APPSwDI/mNos2 FUTURE EXPERIMENTS AND VALIDATION STUDIES: Future research should determine the extent to which prevention of surgery-induced microgliosis and/or neurovascular unit dysfunction can prevent or ameliorate postoperative memory and attention deficits in animal models. Translational human studies should evaluate perioperative indices of innate immunity and neurovascular integrity and assess their potential link to perioperative neurocognitive disorders. MAJOR CHALLENGES FOR THE HYPOTHESIS: Understanding the complex relationships between delirium and dementia will require mechanistic studies aimed at evaluating the role of postoperative neuroinflammation and blood-brain barrier changes in the setting of pre-existing neurodegenerative and/or aging-related pathology. LINKAGE TO OTHER MAJOR THEORIES: Non-resolving inflammation with vascular disease that leads to cognitive impairments and dementia is increasingly important in risk stratification for AD in the aging population. The interdependence of these factors with surgery-induced neuroinflammation and cognitive dysfunction is also becoming apparent, providing a strong platform for assessing the relationship between postoperative delirium and longer term cognitive dysfunction in older adults.

Indexed as

InflammationPostoperative ComplicationsAnimalsBlood-Brain BarrierBrainCognition DisordersDeliriumDementiaDisease Models, AnimalHumansMiceNeurocognitive Disordersinflammationinnate immunityneuroinflammationneurovascular unitsurgeryvascular

Identifiers

PMID32291962
PMCPMC7317948
OpenAlexW3015680881

What OpenQuestion holds

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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.