Evidence map›Paper›PMID 32147052›Full record

ArticleComplementary therapies in medicine2020

Autonomically-mediated decrease in microvascular blood flow due to mental stress and pain in sickle cell disease: A target for neuromodulatory interventions.

Sarah R Martin, Payal Shah, Christopher Denton, Lonnie K Zeltzer, Saranya Veluswamy, Michael C K Khoo, Thomas D Coates

Open access · greenAbstract read
In one paragraph

Article in Complementary therapies in medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Analysis ofFrontiers in pain research (Lausanne, Switzerland) · 2022
    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

7 authors at 3 institutions in 1 country.

Sarah R MartinPediatric Pain Research Program, Division of Hematology-Oncology, Department of Pediatrics, David Geffen School of Medicine at UCLA, 650 Charles E. Young S., #12-096 CHS, Los Angeles, CA, 90095, USA.
Payal ShahDivision of Hematology, Children's Center for Cancer and Blood Diseases, Children's Hospital Los Angeles, Keck School of Medicine, University of Southern California, 4650 Sunset Blvd, Mailstop #64, Los Angeles, CA, 90027, USA.
Christopher DentonDivision of Hematology, Children's Center for Cancer and Blood Diseases, Children's Hospital Los Angeles, Keck School of Medicine, University of Southern California, 4650 Sunset Blvd, Mailstop #64, Los Angeles, CA, 90027, USA.
Lonnie K ZeltzerPediatric Pain Research Program, Division of Hematology-Oncology, Department of Pediatrics, David Geffen School of Medicine at UCLA, 650 Charles E. Young S., #12-096 CHS, Los Angeles, CA, 90095, USA.
Saranya VeluswamyDivision of Hematology, Children's Center for Cancer and Blood Diseases, Children's Hospital Los Angeles, Keck School of Medicine, University of Southern California, 4650 Sunset Blvd, Mailstop #64, Los Angeles, CA, 90027, USA.
Michael C K KhooDepartment of Biomedical Engineering, Viterbi School of Engineering, University of Southern California, Corwin D. Denney Research Center, 1042 Downey Way, Los Angeles, CA, 90089, USA.
Thomas D CoatesDivision of Hematology, Children's Center for Cancer and Blood Diseases, Children's Hospital Los Angeles, Keck School of Medicine, University of Southern California, 4650 Sunset Blvd, Mailstop #64, Los Angeles, CA, 90027, USA. Electronic address: TCoates@chla.usc.edu.
Children's Hospital of Los Angeles · USUniversity of California, Los Angeles · USUniversity of Southern California · US

Funding

TrainingP41EB001978 · NIBIB · UNIVERSITY OF SOUTHERN CALIFORNIA · PI KHOO, MICHAEL C K · 2003 to 2017
$18.1M
Neuromodulatory Mechanisms and Regional Autonomic Dysregulation in the Development of Pain in Sickle Cell Disease PatientsU01HL117718 · NHLBI · CHILDREN'S HOSPITAL OF LOS ANGELES · PI COATES, THOMAS DUANE, KHOO, MICHAEL C K · 2013 to 2017
$9.6M
A laboratory-based hypnosis intervention on psychophysiological markers of pain responsivity in adolescents with and without sickle cell diseaseF32HL139114 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MARTIN, SARAH R · 2017 to 2020
$192k
NHLBI NIH HHS F32 HL139114NHLBI NIH HHS U01 HL117718NIBIB NIH HHS P41 EB001978
6 · The paper itself

Abstract

Pain and vaso-occlusive crises (VOC) are hallmark complications of sickle cell disease (SCD) and result in significant physical and psychosocial impairment. The variability in SCD pain frequency and triggers for the transition from steady state to VOC are not well understood. This paper summarizes the harmful physiological effects of pain and emotional stressors on autonomically-mediated vascular function in individuals with SCD and the effects of a cognitive, neuromodulatory intervention (i.e. hypnosis) on microvascular blood flow. We reviewed recent studies from the authors' vascular physiology laboratory that assessed microvascular responses to laboratory stressors in individuals with SCD. Results indicate that participants with SCD exhibit marked neurally mediated vascular reactivity in response to pain, pain-related fear, and mental stress. Further, pilot study results show that engagement in hypnosis may attenuate harmful microvascular responses to pain. The collective results demonstrate that autonomically-mediated vascular responses to pain and mental stress represent an important SCD intervention target. This ongoing work provides physiological justification for the inclusion of cognitive, neuromodulatory and complementary treatments in SCD disease management and may inform the development of targeted, integrative interventions that prevent the enhancement of autonomic vascular dysfunction in SCD.

Indexed as

MicrocirculationAnemia, Sickle CellHumansHypnosisPainPain ManagementStress, PsychologicalAnxietyAutonomic nervous systemHypnosisNeuromodulatory treatmentPainSickle cell diseaseStressVasoconstrictionVaso-occlusive crises

Identifiers

PMID32147052
PMCPMC7640987
OpenAlexW3005984622

What OpenQuestion holds

Textmetadata
LicenceTDM
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.