Evidence map›Paper›PMID 17008408›Full record

Trial reportProceedings of the National Academy of Sciences of the United States of America2006

Phosphodiesterase genes are associated with susceptibility to major depression and antidepressant treatment response.

Ma-Li Wong, Fiona Whelan, Panagiotis Deloukas, Pamela Whittaker, Marcos Delgado, Rita M Cantor, Samuel M McCann, Julio Licinio

Open access · greenAbstract readClinical Trial, Phase IRandomized Controlled Trial
In one paragraph

Trial report in Proceedings of the National Academy of Sciences of the United States of America, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 2 pooled it
5.7field-weighted citation impact, top 3% 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

61 citing papers in PubMed, 2 syntheses or guidelines pooled it, 151 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Trial
  6. Trial
  7. Radiosynthesis and Preclinical Evaluation of a NovelACS medicinal chemistry letters · 2026
    Article
  8. Epigenetic Signatures of Social Defeat Stress Varying Duration.International journal of molecular sciences · 2025
    Article
  9. Article
  10. Phosphodiesterases: Evolving Concepts and Implications for Human Therapeutics.Annual review of pharmacology and toxicology · 2025
    Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
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  18. Article
  19. Review
  20. Article

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

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 4 institutions in 2 countries.

Ma-Li WongCenter on Pharmacogenomics, Department of Psychiatry and Behavioral Sciences, Miller School of Medicine, University of Miami, Miami, FL 33136, USA. mali@miami.edu
Fiona Whelan
Panagiotis Deloukas
Pamela Whittaker
Marcos Delgado
Rita M Cantor
Samuel M McCann
Julio Licinio
Wellcome Sanger Institute · GBUniversity of Miami · USPennington Biomedical Research Center · USUniversity of California, Los Angeles · US

Funding

ZDV &3TC NEVIRAPINE COMBINATION THERAPY IN HIV 1 INFECTED INFANTS &M01RR000865 · NCRR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WASHINGTON, ARNOLD E. · 1985 to 2011
$43.4M
UCLA Mentored Clinical Pharmacology Research Scholar Pr*K12RR017611 · NCRR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LEVEY, BARBARA ANN · 2002 to 2006
$5.0M
UCLA PHARMACOGENETICS &PHARMACOGENOMICS RESEARCH GROUPU01GM061394 · NIGMS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI LICINIO, JULIO · 2000 to 2005
$4.7M
Depression/Metabolic Syndrome in Mexican-American Women.R01DK063240 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI WONG, MA-LI · 2002 to 2006
$1.9M
UCLA GRADUATE TRAINING PROGRAM IN TRANSITIONAL INVESTIGAK30HL004526 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LICINIO, JULIO · 2000 to 2004
$995k
Pharmacogenetics of Antidepressant DrugsK24RR017365 · NCRR · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI WONG, MA-LI · 2003 to 2007
$727k
Clinical Neuroendocrinology of LeptinK24RR016996 · NCRR · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI LICINIO, JULIO · 2002 to 2006
$662k
Developing Educational Approaches for Mexican-AmericansR03HG002500 · NHGRI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LICINIO, JULIO · 2002 to 2005
$392k
CNS transcription modulation in peripheral inflammationR21MH062777 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WONG, MA-LI · 2001 to 2002
$306k
NCRR NIH HHS K12 RR017611NCRR NIH HHS K12RR17611NCRR NIH HHS K24 RR016996NCRR NIH HHS K24 RR017365NCRR NIH HHS M01 RR000865NCRR NIH HHS RR000865NCRR NIH HHS RR017365NCRR NIH HHS RR16996NHGRI NIH HHS HG002500NHGRI NIH HHS R03 HG002500NHLBI NIH HHS K30 HL004526NHLBI NIH HHS K30HL04526NIDDK NIH HHS DK063240NIDDK NIH HHS R01 DK063240NIGMS NIH HHS GM61394NIGMS NIH HHS U01 GM061394NIMH NIH HHS MH062777Wellcome Trust
6 · The paper itself

Abstract

Cyclic nucleotide phosphodiesterases (PDEs) constitute a family of enzymes that degrade cAMP and cGMP. Intracellular cyclic nucleotide levels increase in response to extracellular stimulation by hormones, neurotransmitters, or growth factors and are down-regulated through hydrolysis catalyzed by PDEs, which are therefore candidate therapeutic targets. cAMP is a second messenger implicated in learning, memory, and mood, and cGMP modulates nervous system processes that are controlled by the nitric oxide (NO)/cGMP pathway. To investigate an association between genes encoding PDEs and susceptibility to major depressive disorder (MDD), we genotyped SNPs in 21 genes of this superfamily in 284 depressed Mexican Americans who participated in a prospective, double-blind, pharmacogenetic study of antidepressant response, and 331 matched controls. Polymorphisms in PDE9A and PDE11A were found to be associated with the diagnosis of MDD. Our data are also suggestive of the association between SNPs in other PDE genes and MDD. Remission on antidepressants was significantly associated with polymorphisms in PDE1A and PDE11A. Thus, we found significant associations with both the diagnosis of MDD and remission in response to antidepressants with SNPs in the PDE11A gene. We show here that PDE11A haplotype GAACC is significantly associated with MDD. We conclude that PDE11A has a role in the pathophysiology of MDD. This study identifies a potential CNS role for the PDE11 family. The hypothesis that drugs affecting PDE function, particularly cGMP-related PDEs, represent a treatment strategy for major depression should therefore be tested.

Indexed as

Genetic Predisposition to Disease3',5'-Cyclic-GMP PhosphodiesterasesAdultAgedAntidepressive AgentsCyclic Nucleotide Phosphodiesterases, Type 1DesipramineDouble-Blind MethodFemaleFluoxetineHumansMajor Depressive DisorderMaleMexican AmericansMiddle AgedPhosphoric Diester Hydrolases3',5'-Cyclic-GMP PhosphodiesterasesAntidepressive AgentsCyclic Nucleotide Phosphodiesterases, Type 1DesipramineFluoxetinePDE11A protein, humanPDE1A protein, humanPhosphoric Diester Hydrolases

Identifiers

PMID17008408
PMCPMC1581426
OpenAlexW1990017678

What OpenQuestion holds

Textmetadata
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.