Evidence map›Paper›PMID 31707310›Full record

ArticleComprehensive psychiatry2020

Longitudinal population subgroups of CRP and risk of depression in the ALSPAC birth cohort.

Emanuele F Osimo, Jan Stochl, Stan Zammit, Glyn Lewis, Peter B Jones, Golam M Khandaker

Open access · goldAbstract read
In one paragraph

Article in Comprehensive psychiatry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
0.9field-weighted citation impact, top 30% 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

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 27 citations in OpenAlex.

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  14. C-Reactive Protein as a Biomarker for Major Depressive Disorder?International journal of molecular sciences · 2022
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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 at 4 institutions in 2 countries.

Emanuele F OsimoDepartment of Psychiatry, University of Cambridge, Cambridge, UK; Cambridgeshire and Peterborough NHS Foundation Trust, Cambridge, UK; Institute of Clinical Sciences, Imperial College London, London, UK. Electronic address: efo22@cam.ac.uk.
Jan StochlDepartment of Psychiatry, University of Cambridge, Cambridge, UK; Department of Kinanthropology, Charles University, Prague, Czech Republic.
Stan ZammitCentre for Academic Mental Health, Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK; Division of Psychiatry, University College London, London, UK.
Glyn LewisDivision of Psychiatry, University College London, London, UK.
Peter B JonesDepartment of Psychiatry, University of Cambridge, Cambridge, UK; Cambridgeshire and Peterborough NHS Foundation Trust, Cambridge, UK.
Golam M KhandakerDepartment of Psychiatry, University of Cambridge, Cambridge, UK; Cambridgeshire and Peterborough NHS Foundation Trust, Cambridge, UK.
University of Cambridge · GBCharles University · CZUniversity College London · GBUniversity of Bristol · GB

Funding

Maternal overnutrition and offspring fat mass, metabolic and vascular function.R01DK077659 · NIDDK · UNIVERSITY OF BRISTOL · PI LAWLOR, DEBORAH ANNE · 2006 to 2009
$986k
Medical Research Council G0801456Medical Research Council G9815508Medical Research Council MC_PC_17213Medical Research Council MC_PC_19009Medical Research Council MR/L010305/1NIDDK NIH HHS R01 DK077659Wellcome TrustWellcome Trust 08426812/Z/07/ZWellcome Trust 088869/Z/09/ZWellcome Trust 095844/Z/11/ZWellcome Trust 102215/2/13/2Wellcome Trust 201486/Z/16/Z
6 · The paper itself

Abstract

backgroundMeta-analyses confirm increased circulating C-reactive protein (CRP) levels in depression. Longitudinal studies have linked one-off measurements of CRP at baseline with increased risk of developing depressive symptoms subsequently at follow-up, but studies with repeat CRP measures from the same individuals are scarce.

methodsWe have examined whether longitudinal patterns of inflammation, based on three CRP measurements from childhood to early-adulthood, are associated with the risk of depression in early-adulthood in the Avon Longitudinal Study of Parents and Children, a prospective birth cohort.

resultsUsing Gaussian mixture modelling of available CRP data from age 9, 15 and 18 years, we identified four population clusters/sub-groups reflecting different longitudinal patterns of CRP: persistently low (N=463, 29.5%); persistently high (N=371, 24%); decreasing (N=360, 23%); increasing (N=367, 23.5%). The increasing group showed a steep increase in CRP levels between adolescence and early-adulthood. Participants in this group had a higher risk of moderate/severe depression at age 18 years, compared with those with persistently low CRP; adjusted odds ratio (OR)=3.78 (95% Confidence Interval (CI), 1.46-9.81; p=0.006). The odds of moderate/severe depression were also increased for the persistently high CRP group, but this was not statistically significant; OR=2.54 (95% CI, 0.90-7.16). LIMITATIONS: Repeat CRP measures were available for a subset, who may not be representative of all cohort participants.

conclusionsThe results suggest that an increasing pattern of inflammation from adolescence to early-adulthood is associated with risk of depression in early-adulthood.

Indexed as

AdolescentAdultChildCohort StudiesC-Reactive ProteinDepressionDepressive DisorderFemaleHumansLongitudinal StudiesMaleProspective StudiesRiskC-Reactive ProteinALSPACC-reactive proteinCRPDepressionImmunopsychiatryInflammation

Identifiers

PMID31707310
PMCPMC6945112
OpenAlexW2984556316

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.