Evidence map›Paper›PMID 30836325›Full record

ArticleNeuroImage. Clinical2019

Divergent patterns of loss of interpersonal warmth in frontotemporal dementia syndromes are predicted by altered intrinsic network connectivity.

Gianina Toller, Winson F Z Yang, Jesse A Brown, Kamalini G Ranasinghe, Suzanne M Shdo, Joel H Kramer, William W Seeley, Bruce L Miller, Katherine P Rankin

Abstract read
In one paragraph

Article in NeuroImage. Clinical, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Review
  3. High-frequency assessment of mood, personality, and cognition in healthy younger, healthy older and adults with cognitive impairment.Neuropsychology, development, and cognition. Section B, Aging, neuropsychology and cognition · 2024
    Article
  4. Article
  5. Semantic knowledge of social interactions is mediated by the hedonic evaluation system in the brain.Cortex; a journal devoted to the study of the nervous system and behavior · 2023
    Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
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

9 authors.

Gianina TollerDepartment of Neurology, Memory and Aging Center, Weill Institute for Neurosciences, University of California, San Francisco, USA. Electronic address: gianina.toller@ucsf.edu.
Winson F Z YangDepartment of Neurology, Memory and Aging Center, Weill Institute for Neurosciences, University of California, San Francisco, USA. Electronic address: winson.yang@alumni.maastrichtuniversity.nl.
Jesse A BrownDepartment of Neurology, Memory and Aging Center, Weill Institute for Neurosciences, University of California, San Francisco, USA. Electronic address: jesse.brown@ucsf.edu.
Kamalini G RanasingheDepartment of Neurology, Memory and Aging Center, Weill Institute for Neurosciences, University of California, San Francisco, USA. Electronic address: kamalini.ranasinghe@ucsf.edu.
Suzanne M ShdoDepartment of Neurology, Memory and Aging Center, Weill Institute for Neurosciences, University of California, San Francisco, USA. Electronic address: suzanne.shdo@ucsf.edu.
Joel H KramerDepartment of Neurology, Memory and Aging Center, Weill Institute for Neurosciences, University of California, San Francisco, USA. Electronic address: joel.kramer@ucsf.edu.
William W SeeleyDepartment of Neurology, Memory and Aging Center, Weill Institute for Neurosciences, University of California, San Francisco, USA. Electronic address: bill.seeley@ucsf.edu.
Bruce L MillerDepartment of Neurology, Memory and Aging Center, Weill Institute for Neurosciences, University of California, San Francisco, USA. Electronic address: bruce.miller@ucsf.edu.
Katherine P RankinDepartment of Neurology, Memory and Aging Center, Weill Institute for Neurosciences, University of California, San Francisco, USA. Electronic address: kate.rankin@ucsf.edu.

Funding

TDP-43 Loss-of-Function: Biology to BiomarkersP01AG019724 · NIA · UNIVERSITY OF PENNSYLVANIA · PI BRUCE L MILLER · 2002 to 2026
$67.2M
PrPSc SPECIFIC INTERACTION WITH NOVEL PrP-Fc FUSION PROTEINSP50AG023501 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MILLER, BRUCE L · 2004 to 2018
$27.1M
Mechanisms of Executive Decline in Normal AgingR01AG032289 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Kaitlin B Casaletto, JOEL H KRAMER · 2009 to 2026
$8.3M
Biological Predictors Of Brain Aging Trajectories Diversity Supplement: African American Outreach And The Intersection Between Social Determinants Of Health And Biomarkers Of Degenerative DiseaseRF1AG032289 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KRAMER, JOEL H · 2020 to 2021
$5.3M
Attention and Semantic Evaluation as Predictors of Empathy in Healthy Aging and Frontotemporal DementiaRF1AG029577 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI RANKIN, KATHERINE P · 2019 to 2019
$4.0M
Measuring Altered Social Behavior in Neurodegenerative DiseaseR01AG029577 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI RANKIN, KATHERINE P · 2008 to 2018
$3.6M
Neurophysiological Assessments of Network Dysfunction in Alzheimer's DiseaseK08AG058749 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI RANASINGHE, KAMALINI GAYATHREE · 2019 to 2023
$859k
Patient-tailored network prediction of neurodegenerative disease progressionK01AG055698 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BROWN, JESSE AARON · 2017 to 2022
$779k
Neuroanatomy of social Function in FTDK23AG021606 · NIA · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI RANKIN, KATHERINE P · 2003 to 2005
$204k
NIA NIH HHS K01 AG055698NIA NIH HHS K08 AG058749NIA NIH HHS K23 AG021606NIA NIH HHS P01 AG019724NIA NIH HHS P50 AG023501NIA NIH HHS R01 AG029577NIA NIH HHS R01 AG032289NIA NIH HHS RF1 AG029577NIA NIH HHS RF1 AG032289
6 · The paper itself

Abstract

Loss of warmth is well-documented in behavioral variant frontotemporal dementia (bvFTD) and semantic variant primary progressive aphasia (svPPA) at a group level, and has been linked to salience (SN) and semantic-appraisal (SAN) network atrophy. However, clinical observations of individual patients show much greater heterogeneity, thus measuring this clinical variability and identifying the underlying neurologic mechanisms is a critical step for understanding the symptom profile of any one patient. We used reliable change indexes with premorbid and current informant-based evaluations to characterize patterns of change on the warmth subscale of the Interpersonal Adjective Scale (IAS) questionnaire in 132 patients (21 bvFTD, 19 svPPA, 22 nonfluent variant primary progressive aphasia [nfvPPA], 37 Alzheimer's disease [AD]) and 33 healthy older adults. We investigated whether individual differences in warmth change were reflected in SN or SAN functional connectivity, or structural volume of individual brain regions in these two networks. Though one subset of patients showed significant drop in warmth to abnormally low levels (bvFTD: 38%; svPPA: 21%; nfvPPA: 5%; AD: 11%), a second subset significantly dropped but remained within the clinically normal range (bvFTD: 33%; svPPA: 21%; nfvPPA: 9%; AD: 5%), and a third subset did not drop and stayed in the clinically normal range (bvFTD: 29%; svPPA: 58%; nfvPPA: 86%; AD: 84%). Furthermore, interpersonal warmth score was strongly predicted by SN functional connectivity (p < .01), but not by SAN functional connectivity or by structural volume in these networks. Our results extend earlier group-level findings by showing wide individual variability in degree of disease-related reduction of interpersonal warmth and SN functional connectivity in bvFTD and svPPA, and highlight new approaches to revealing how brain connectivity predicts behavior on an individual patient level. Our findings suggest that measures of interpersonal warmth can provide important clinical information about changes in underlying brain networks, and help clinicians and clinical researchers better identify which bvFTD and svPPA patients are at greater risk for interpersonal disruption.

Indexed as

Social SkillsAgedFemaleFrontotemporal DementiaHumansMaleMiddle AgedNerve NetPredictive Value of TestsBehavioral variant frontotemporal dementiaInterpersonal warmthResting-state fMRISalience networkSemantic-appraisal networkSemantic variant primary progressive aphasia

Identifiers

PMID30836325
PMCPMC6403437

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.