Evidence map›Paper›PMID 25603415›Full record

ArticleTranslational psychiatry2015

C-reactive protein gene variants: independent association with late-life depression and circulating protein levels.

M-L Ancelin, A Farré, I Carrière, K Ritchie, I Chaudieu, J Ryan

Abstract read
In one paragraph

Article in Translational psychiatry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

25 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Genetic Contributions of Inflammation to Depression.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2017
    Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. C-Reactive Protein as a Biomarker for Major Depressive Disorder?International journal of molecular sciences · 2022
    Review
  9. Article
  10. Review
  11. The association between C-reactive protein, mood disorder, and cognitive function in UK Biobank.European psychiatry : the journal of the Association of European Psychiatrists · 2021
    Article
  12. Article
  13. Article
  14. Article
  15. 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

6 authors.

M-L Ancelin1] Inserm, U1061, Hopital La Colombiere, Montpellier, France [2] Université Montpellier 1, U1061, Montpellier, France.
A Farré1] Inserm, U1061, Hopital La Colombiere, Montpellier, France [2] Université Montpellier 1, U1061, Montpellier, France.
I Carrière1] Inserm, U1061, Hopital La Colombiere, Montpellier, France [2] Université Montpellier 1, U1061, Montpellier, France.
K Ritchie1] Inserm, U1061, Hopital La Colombiere, Montpellier, France [2] Université Montpellier 1, U1061, Montpellier, France [3] Faculty of Medicine, Imperial College, London, UK.
I Chaudieu1] Inserm, U1061, Hopital La Colombiere, Montpellier, France [2] Université Montpellier 1, U1061, Montpellier, France.
J Ryan1] Inserm, U1061, Hopital La Colombiere, Montpellier, France [2] Université Montpellier 1, U1061, Montpellier, France [3] Disease Epigenetics Group, Murdoch Children's Research Institute, Parkville, VIC, Australia [4] Department of Paediatrics, The University of Melbourne, Parkville, VIC, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

C-reactive protein (CRP) is a heritable biomarker of systemic inflammation that is commonly elevated in depressed patients. Variants in the CRP gene that influence protein levels could thus be associated with depression but this has seldom been examined, especially in the elderly. Depression was assessed in 990 people aged at least 65 years as part of the ESPRIT study. A clinical level of depression (DEP) was defined as having a score of ⩾16 on The Center for Epidemiologic Studies Depression scale or a diagnosis of current major depression based on the Mini-International Neuropsychiatric Interview and according to Diagnostic and Statistical Manual of Mental Disorders-IV criteria. Five single-nucleotide polymorphisms spanning the CRP gene were genotyped, and circulating levels of high-sensitivity CRP were determined. Multivariable analyses adjusted for socio-demographic characteristics, smoking, ischemic pathologies, cognitive impairment and inflammation-related chronic pathologies. The minor alleles of rs1130864 and rs1417938 were associated with a decreased risk of depression in women at Bonferroni-corrected significance levels (P=0.002). CRP gene variants were associated with serum levels in a gender-specific manner, but only rs1205 was found to be nominally associated with both an increased risk of DEP and lower circulating CRP levels in women. Variants of the CRP gene thus influence circulating CRP levels and appear as independent susceptibility factors for late-life depression.

Indexed as

AgedAge FactorsAntidepressive AgentsC-Reactive ProteinDepressive DisorderFemaleGenetic Predisposition to DiseaseHumansMajor Depressive DisorderMaleMultivariate AnalysisPolymorphism, Single NucleotideAntidepressive AgentsC-Reactive Protein

Identifiers

PMID25603415
PMCPMC4312833

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Registered trials

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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.