Evidence map›Paper›PMID 27888772›Full record

ArticlePsychoneuroendocrinology2017

Adrenocortical sensitivity, moderated by ongoing stress, predicts drinking intensity in alcohol-dependent men.

Bryon Adinoff, David Leonard, Julianne Price, Martin A Javors, Robrina Walker, E Sherwood Brown, Hong Xiao, Uma Rao

Open access · greenAbstract read
In one paragraph

Article in Psychoneuroendocrinology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 42% 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

5 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
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

8 authors at 3 institutions in 1 country.

Bryon AdinoffVA North Texas Health Care System, Dallas, TX, USA; Department of Psychiatry, University of Texas Southwestern Medical Center, Dallas, TX, USA. Electronic address: Bryon.adinoff@utsouthwestern.edu.
David LeonardDavid Leonard Statistical Consulting, Wichita Falls, TX, USA.
Julianne PriceDepartment of Psychiatry, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Martin A JavorsDepartment of Psychiatry, University of Texas Health Science Center, 7703 Floyd Curl Drive, San Antonio, TX 78229, USA.
Robrina WalkerDepartment of Psychiatry, University of Texas Southwestern Medical Center, Dallas, TX, USA.
E Sherwood BrownDepartment of Psychiatry, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Hong XiaoFairway Family Medicine, Carrollton, TX, USA.
Uma RaoCenter for Behavioral Health Research, University of Tennessee, Knoxville, TN, USA; Department of Pediatrics and Vanderbilt Kennedy Center, Vanderbilt University Medical Center, Nashville, TN, USA.
The University of Texas Southwestern Medical Center · USThe University of Texas Health Science Center at San Antonio · USVanderbilt University Medical Center · US

Funding

UT Southwestern Center for Translational Medicine (UL1/KL2/TL1)UL1TR001105 · NCATS · UT SOUTHWESTERN MEDICAL CENTER · PI TOTO, ROBERT DANIEL · 2013 to 2017
$24.5M
UT-Southwestern Clinical and Translational Alliance for Research (UT-STAR) (TL1)UL1TR000451 · NCATS · UT SOUTHWESTERN MEDICAL CENTER · PI TOTO, ROBERT DANIEL · 2012 to 2012
$6.3M
Risk for Substance Abuse in Depressed AdolescentsR01MH062464 · NIMH · UT SOUTHWESTERN MEDICAL CENTER · PI RAO, UMA · 2001 to 2006
$2.4M
Stress Response and Smoking Cessation in Depressed YouthR01DA015131 · NIDA · UT SOUTHWESTERN MEDICAL CENTER · PI RAO, UMA · 2003 to 2007
$2.4M
Markers of Risk for Nicotine Dependence in YoungstersR01DA014037 · NIDA · UT SOUTHWESTERN MEDICAL CENTER · PI RAO, UMA · 2001 to 2006
$1.9M
Stress, HPA Axis Dysfunction, and Relapse in AlcoholismU01AA016668 · NIAAA · UT SOUTHWESTERN MEDICAL CENTER · PI ADINOFF, BRYON H. · 2007 to 2011
$1.7M
Treatment Prediction in Adolescent and Adult DepressionR01MH068391 · NIMH · UT SOUTHWESTERN MEDICAL CENTER · PI RAO, UMA · 2004 to 2012
$1.7M
Stress and Risk for Substance Abuse in AdolescentsR01DA017804 · NIDA · UT SOUTHWESTERN MEDICAL CENTER · PI RAO, UMA · 2004 to 2008
$1.6M
Neuronal Risk Markers for Nicotine Dependence in YouthR01DA017805 · NIDA · UT SOUTHWESTERN MEDICAL CENTER · PI RAO, UMA · 2004 to 2010
$1.4M
NCATS NIH HHS UL1 TR000451NCATS NIH HHS UL1 TR001105NIAAA NIH HHS U01 AA016668NIDA NIH HHS R01 DA014037NIDA NIH HHS R01 DA015131NIDA NIH HHS R01 DA017804NIDA NIH HHS R01 DA017805NIMH NIH HHS R01 MH062464NIMH NIH HHS R01 MH068391
6 · The paper itself

Abstract

Allostatic load from both environmental stressors and persistent glucocorticoid secretion has been associated with disease severity in alcohol dependence. Heightened relapse risk and/or drinking severity, in particular, may be a reaction to alcohol- and withdrawal-induced changes in physiological stress response systems coupled with ongoing life stress, although their shared contributions upon drinking severity have not been assessed. To investigate the combined contribution of hypothalamic-pituitary-adrenal (HPA) reactivity and environmental stressors (e.g., ongoing life stress) to relapse severity in alcohol-dependent men following treatment, plasma adrenocorticotropin (ACTH) and cortisol were obtained in 4-6 weeks abstinent alcohol-dependent men (n=41) following a psychosocial stressor [the Trier Social Stress Test (TSST)] and two pharmacological provocations [ovine corticotropin releasing factor (oCRH) and cosyntropin]. Following treatment discharge, drinking outcomes (primary outcome: drinks per drinking day (DDD); secondary outcomes: total drinks and drinking days) were assessed weekly and ongoing life stress was assessed biweekly for 24 weeks following treatment discharge. Generalized estimating equation models of drinking severity were fit with basal and stimulated ACTH and cortisol concentrations as predictors and ongoing life stress as the moderator. Greater levels of life stress were independently associated with greater drinking intensity (DDD and total drinks) but not frequency (days drinking). Higher basal cortisol:ACTH or provoked cortisol:ACTH ratios were strongly associated with greater post-treatment DDD in individuals who experienced higher levels of ongoing stress. In conclusion, ongoing life stress is associated with post-treatment drinking intensity in alcohol dependent men; stress also strengthens the relationship between adrenocortical sensitivity and post-treatment drinking. Physiological measures of allostatic load and environmental stressors conjointly increase relapse intensity.

Indexed as

AlcoholismHypothalamo-Hypophyseal SystemPituitary-Adrenal SystemSeverity of Illness IndexStress, PsychologicalAdrenocorticotropic HormoneAdultDrinking BehaviorHumansHydrocortisoneMaleMiddle AgedYoung AdultAdrenocorticotropic HormoneHydrocortisoneAlcoholismCortisolHPARelapseStress

Identifiers

PMID27888772
PMCPMC5272781
OpenAlexW2547199382

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.