Evidence map›Paper›PMID 22869065›Full record

Trial reportArchives of neurology2012

Effects of growth hormone–releasing hormone on cognitive function in adults with mild cognitive impairment and healthy older adults: results of a controlled trial.

Laura D Baker, Suzanne M Barsness, Soo Borson, George R Merriam, Seth D Friedman, Suzanne Craft, Michael V Vitiello

Registry-linked trialOpen access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Archives of neurology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00257712 (GHRH), which is not on this map. Cited by 74 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed, 3 pooled it
5.2field-weighted citation impact, top 4% 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.

NCT00257712 phase2completednot on this map

GHRH: Cognition in Aging and MCI

TypeinterventionalSponsorUniversity of WashingtonRan2006 to 2011Enrolled151ConditionsAging, Mild Cognitive ImpairmentArmsTH9507 human growth hormone releasing hormone (GHRH)
3 · Its place in the literature

Who cites it

74 citing papers in PubMed, 3 syntheses or guidelines pooled it, 133 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Trial
  6. Trial
  7. Trial
  8. Trial
  9. Trial
  10. Article
  11. Article
  12. Review
  13. Article
  14. Plasma proteomic analysis identifies proteins and pathways related to Alzheimer's risk.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
  15. GHRH and its analogues in central nervous system diseases.Reviews in endocrine & metabolic disorders · 2025
    Review
  16. Review
  17. Review
  18. Review
  19. Review
  20. Review

14 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Laura D BakerDepartment of Psychiatry and Behavioral Science, University of Washington School of Medicine, USA. ldbaker@uw.edu
Suzanne M Barsness
Soo Borson
George R Merriam
Seth D Friedman
Suzanne Craft
Michael V Vitiello
University of Washington · USSeattle Children's Hospital · US

Funding

ZIPRASIDONE IN NORMAL HEPATIC FUNCTION SUBJECTS &IN HEPATIC DYSFUCTIN SUBJECTSM01RR000037 · NCRR · UNIVERSITY OF WASHINGTON · PI PIHOKER, CATHERINE · 1985 to 2007
$33.8M
GHRH: COGNITION IN AGING AND MILD COGNITIVE IMPAIRMENTR01AG025515 · NIA · UNIVERSITY OF WASHINGTON · PI VITIELLO, MICHAEL V. · 2005 to 2009
$2.5M
GHRH: Cellular Integrity in Aging and Mild Cognitive ImpairmentR01AG030484 · NIA · SEATTLE CHILDREN'S HOSPITAL · PI FRIEDMAN, SETH DAVID · 2009 to 2011
$835k
NCRR NIH HHS M01 RR000037NIA NIH HHS AG025515NIA NIH HHS AG030484NIA NIH HHS R01 AG025515NIA NIH HHS R01 AG030484PHS HHS ULRR025014
6 · The paper itself

Abstract

backgroundGrowth hormone–releasing hormone(GHRH), growth hormone, and insulin like growth factor 1 have potent effects on brain function, their levels decrease with advancing age, and they likely play a role in the pathogenesis of Alzheimer disease. Previously, we reported favorable cognitive effects of short-term GHRH administration in healthy older adults and provided preliminary evidence to suggest a similar benefit in adults with mild cognitive impairment (MCI).

objectiveTo examine the effects of GHRH on cognitive function in healthy older adults and in adults with MCI.

designRandomized,double-blind,placebo-controlled trial.

settingClinical Research Center, University of Washington School of Medicine in Seattle.

participantsA total of 152 adults (66 with MCI) ranging in age from 55 to 87 years (mean age, 68 years); 137 adults (76 healthy participants and 61 participants with MCI) successfully completed the study.

interventionParticipants self-administered daily subcutaneous injections of tesamorelin (Theratechnologies Inc),a stabilized analog of human GHRH (1 mg/d), or placebo 30 minutes before bedtime for 20 weeks. At baseline, at weeks 10 and 20 of treatment, and after a 10-week washout(week 30), blood samples were collected, and parallel versions of a cognitive battery were administered. Before and after the 20-week intervention, participants completed an oral glucose tolerance test and a dual-energy x-ray absorptiometry scan to measure body composition.

main outcome measuresPrimary cognitive outcomes were analyzed using analysis of variance and included 3 composites reflecting executive function, verbal memory, and visual memory. Executive function was assessed with Stroop Color-Word Interference,Task Switching, the Self-Ordered Pointing Test, and Word Fluency, verbal memory was assessed with Story Recall and the Hopkins Verbal Learning Test,and visual memory was assessed with the Visual-Spatial Learning Test and Delayed Match-to-Sample.

resultsThe intent-to-treat analysis indicated a favorable effect of GHRH on cognition (P=.03), which was comparable in adults with MCI and healthy older adults.The completer analysis showed a similar pattern, with a more robust GHRH effect (P=.002). Subsequent analyses indicated a positive GHRH effect on executive function (P=.005) and a trend showing a similar treatment-related benefit in verbal memory(P=.08). Treatment with GHRH increased insulin like growth factor 1 levels by 117 %(P.001), which remained within the physiological range, and reduced percent body fat by 7.4%(P.001). Treatment with GHRH increased fasting insulin levels within the normal range by 35%in adults with MCI (P.001) but not in healthy adults. Adverse events were mild and were reported by 68%of GHRH treated adults and 36% of those who received placebo.

conclusionsTwenty weeks of GHRH administration had favorable effects on cognition in both adults with MCI and healthy older adults. Longer-duration treatment trials are needed to further examine the therapeutic potential of GHRH administration on brain health during normal aging and “pathological aging.”

trial registrationclinicaltrials.gov Identifier: NCT00257712

Indexed as

Absorptiometry, PhotonAffectAgedAged, 80 and overBody CompositionCase-Control StudiesCognitive DysfunctionDouble-Blind MethodExecutive FunctionFemaleFollow-Up StudiesGlucose Tolerance TestGrowth Hormone-Releasing HormoneHormonesHumansInsulin-Like Growth Factor IGrowth Hormone-Releasing HormoneHormonesInsulin-Like Growth Factor I

Identifiers

PMID22869065
PMCPMC3764914
OpenAlexW2133969927

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.