Evidence map›Paper›PMID 29298663›Full record

ArticleBMC immunology2018

Association between major depressive disorder and pro-inflammatory cytokines and acute phase proteins among HIV-1 positive patients in Uganda.

Kenneth Musinguzi, Andrew Obuku, Noeline Nakasujja, Harriet Birabwa, Juliet Nakku, Jonathan Levin, Eugene Kinyanda

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in BMC immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 5 pooled it
1.4field-weighted citation impact, top 22% 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

28 citing papers in PubMed, 5 syntheses or guidelines pooled it, 38 citations in OpenAlex.

  1. Examining Depression as a Risk Factor for Cardiovascular Disease in People with HIV: A Systematic Review.Annals of behavioral medicine : a publication of the Society of Behavioral Medicine · 2023
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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

7 authors at 5 institutions in 3 countries.

Kenneth MusinguziMRC/UVRI, Uganda Research Unit on AIDS, P.O. Box 49, Entebbe, Uganda.
Andrew ObukuMRC/UVRI, Uganda Research Unit on AIDS, P.O. Box 49, Entebbe, Uganda.
Noeline NakasujjaDepartment of Psychiatry, Makerere College of Health Sciences, Kampala, Uganda.
Harriet BirabwaButabika National Psychiatric Referral Hospital, Kampala, Uganda.
Juliet NakkuButabika National Psychiatric Referral Hospital, Kampala, Uganda.
Jonathan LevinSchool of Public Health, University of the Witwatersrand, Johannesburg, South Africa.
Eugene KinyandaMRC/UVRI, Uganda Research Unit on AIDS, P.O. Box 49, Entebbe, Uganda. eugene.kinyanda@mrcuganda.org.
Butabika Hospital · UGUganda Virus Research Institute · UGMakerere University · UGUniversity of the Witwatersrand · ZAWellcome Trust · GB

Funding

Medical Research Council MC_U950088495Medical Research Council MR/L004623/1Wellcome Trust 205069/Z/16/Z
6 · The paper itself

Abstract

backgroundMajor depressive disorder (MDD) is a common psychiatric complication of HIV/AIDS. While considerable research has been undertaken to understand the psychosocial risk factors of MDD, there is a paucity of data on its biological risk factors including immunological factors. To address this we undertook a study to investigate the association between MDD and pro-inflammatory cytokines and acute phase proteins among persons living with HIV/AIDS (PLWHA) in Uganda. We collected clinical and laboratory data on 201 PLWHA attending two HIV clinics in central and southwestern Uganda. Clinical data included DSM-IV based MDD diagnosis, while laboratory data included the concentrations of IL-6, TNF-α and CRP measured using ELISA. Multiple logistic linear regression analysis was used to determine which proteins were independently significantly associated with MDD controlling for study site, sex, age and highest educational attainment.

resultsThe prevalence of MDD was 62/201 (30.8%). Adjusting for confounders, the odds of MDD increased with increasing levels of IL-6 [each unit increase in IL-6 titres was associated with an aOR = 0.98 (95% CI, 0.97-0.99); p < 0.001]. Participants with low levels of TNF-α were at reduced risk of MDD compared to participants with no TNF-α [those with a TNF-α of 1- <50 pg/ml titres had an aOR = 0.35(95% CI,0.10-1.16)], but as the level of TNF-α increased, the risk of MDD increased, and in particular participants with high levels of TNF-α (of 500 or above) were at a significantly increased risk of MDD [e.g. those with a TNF-α of 500- < 1000 pg/ml titres had an aOR = 3.98 (95% CI,1.29-12.33)] compared to participants with no TNF-α. There was no evidence that MDD was associated with the level of CRP titres [aOR = 0.95 (0.78-1.15); p = 0.60)].

conclusionIn this study, the pro-inflammatory proteins IL-6 and TNF-α were significantly associated with MDD, while CRP was not.

Indexed as

AdolescentAdultC-Reactive ProteinFemaleHIV-1HIV InfectionsHumansInflammation MediatorsInterleukin-6Logistic ModelsMajor Depressive DisorderMaleMiddle AgedTumor Necrosis Factor-alphaUgandaYoung AdultC-Reactive ProteinInflammation MediatorsInterleukin-6Tumor Necrosis Factor-alphaAcute phase proteinsHIVIl-6Major depressive disorderPro-inflammatory cytokinesTNF-α

Identifiers

PMID29298663
PMCPMC5751544
OpenAlexW2781993597

What OpenQuestion holds

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LicenceCC BY
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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.