Evidence map›Paper›PMID 27429957›Full record

ArticleMolecular neuropsychiatry2016

Leukocyte telomere length predicts SSRI response in major depressive disorder: A preliminary report.

Christina M Hough, F Saverio Bersani, Synthia H Mellon, Elissa S Epel, Victor I Reus, Daniel Lindqvist, Jue Lin, Laura Mahan, Rebecca Rosser, Heather Burke and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular neuropsychiatry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

20 citing papers in PubMed, 42 citations in OpenAlex.

  1. Structural MRI-Based Measures of Accelerated Brain Aging do not Moderate the Acute Antidepressant Response in Late-Life Depression.The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry · 2022
    Trial
  2. Article
  3. The researcher's guide to selecting biomarkers in mental health studies.BioEssays : news and reviews in molecular, cellular and developmental biology · 2024
    Review
  4. Atypical Brain Aging and Its Association With Working Memory Performance in Major Depressive Disorder.Biological psychiatry. Cognitive neuroscience and neuroimaging · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Accelerated brain aging predicts impulsivity and symptom severity in depression.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2021
    Article
  10. Telomere attrition and inflammatory load in severe psychiatric disorders and in response to psychotropic medications.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2020
    Article
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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

14 authors at 2 institutions in 1 country.

Christina M HoughDepartment of Psychiatry, University of California San Francisco (UCSF) School of Medicine, San Francisco, CA, USA.
F Saverio BersaniDepartment of Psychiatry, University of California San Francisco (UCSF) School of Medicine, San Francisco, CA, USA; Department of Neurology and Psychiatry, Sapienza University of Rome, Rome, Italy.
Synthia H MellonDepartment of OB/GYN and Reproductive Science, UCSF School of Medicine, San Francisco, CA, USA.
Elissa S EpelDepartment of Psychiatry, University of California San Francisco (UCSF) School of Medicine, San Francisco, CA, USA.
Victor I ReusDepartment of Psychiatry, University of California San Francisco (UCSF) School of Medicine, San Francisco, CA, USA.
Daniel LindqvistDepartment of Psychiatry, University of California San Francisco (UCSF) School of Medicine, San Francisco, CA, USA; Department of Clinical Sciences, Section for Psychiatry, Lund University, Lund, Sweden.
Jue LinDepartment of Biochemistry and Biophysics, UCSF School of Medicine, San Francisco, CA, USA.
Laura MahanDepartment of Psychiatry, University of California San Francisco (UCSF) School of Medicine, San Francisco, CA, USA.
Rebecca RosserDepartment of Psychiatry, University of California San Francisco (UCSF) School of Medicine, San Francisco, CA, USA.
Heather BurkeDepartment of Psychiatry, University of California San Francisco (UCSF) School of Medicine, San Francisco, CA, USA.
John CoetzeeDepartment of Psychiatry, University of California San Francisco (UCSF) School of Medicine, San Francisco, CA, USA.
J Craig NelsonDepartment of Psychiatry, University of California San Francisco (UCSF) School of Medicine, San Francisco, CA, USA.
Elizabeth H BlackburnDepartment of Biochemistry and Biophysics, UCSF School of Medicine, San Francisco, CA, USA.
Owen M WolkowitzDepartment of Psychiatry, University of California San Francisco (UCSF) School of Medicine, San Francisco, CA, USA.
Center for Neurosciences · USUniversity of California, San Francisco · US

Funding

UCSF CLINICAL AND TRANSLATIONAL SCIENCE INSTITUTEUL1RR024131 · NCRR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI JOHNSTON, S. CLAIBORNE · 2006 to 2011
$111.2M
Cell Aging in Major DepressionR01MH083784 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI EPEL, ELISSA S., MELLON, SYNTHIA H · 2010 to 2020
$6.7M
NCRR NIH HHS UL1 RR024131NIMH NIH HHS R01 MH083784
6 · The paper itself

Abstract

Short leukocyte telomere length (LTL) may be associated with several psychiatric disorders, including major depressive disorder (MDD). Short LTL has previously been associated with poor response to psychiatric medications in bipolar disorder and schizophrenia, but no studies have prospectively assessed the relationship of LTL to SSRI response in MDD. We assessed pre-treatment LTL, depression severity (using the Hamilton Depression Rating Scale [HDRS]), and self-reported positive and negative affect in 27 healthy, unmedicated adults with MDD. Subjects then underwent open-label treatment with a selective serotonin reuptake inhibitor (SSRI) antidepressant for eight weeks, after which clinical ratings were repeated. Analyses were corrected for age, sex and BMI. "Non-responders" to treatment (HDRS improvement <50%) had significantly shorter pre-treatment LTL, compared to "Responders" (p=0.037). Further, shorter pre-treatment LTL was associated with less improvement in negative affect (p<0.010) but not with changes in positive affect (p=0.356). This preliminary study is the first to assess the relationship between LTL and SSRI response in MDD and among the first to prospectively assess its relationship to treatment outcome in any psychiatric illness. Our data suggest that short LTL may serve as a vulnerability index of poorer response to SSRI treatment, but this needs examination in larger samples.

Indexed as

AffectAffective disorderAntidepressantsBiomarkerDepressionMajor depressionMood disordersSelective serotonin reuptake inhibitorsTelomerTreatment response

Identifiers

PMID27429957
PMCPMC4943759
OpenAlexW2473749386

What OpenQuestion holds

Textmetadata
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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.