Evidence map›Paper›PMID 39622992›Full record

ArticleScientific reports2024

Cytokine profiles as predictors of HIV incidence using machine learning survival models and statistical interpretable techniques.

Sarah Ogutu, Mohanad Mohammed, Henry Mwambi

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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

  1. Pooled it
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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

3 authors.

Sarah OgutuSchool of Mathematics, Statistics and Computer Science, University of KwaZulu-Natal, Pietermaritzburg, 3201, South Africa. ogutusarah@gmail.com.
Mohanad MohammedSchool of Mathematics, Statistics and Computer Science, University of KwaZulu-Natal, Pietermaritzburg, 3201, South Africa.
Henry MwambiSchool of Mathematics, Statistics and Computer Science, University of KwaZulu-Natal, Pietermaritzburg, 3201, South Africa.

Funding

Science for Africa Foundation [Grant number DEL-22-009] with support from Wellcome Trust and the UK Foreign, Commonwealth & Development Office and is part of the EDCPT2 programme supported by the European Union. Grant number DEL-22-009Wellcome Trust
6 · The paper itself

Abstract

HIV remains a critical global health issue, with an estimated 39.9 million people living with the virus worldwide by the end of 2023 (according to WHO). Although the epidemic's impact varies significantly across regions, Africa remains the most affected. In the past decade, considerable efforts have focused on developing preventive measures, such as vaccines and pre-exposure prophylaxis, to combat sexually transmitted HIV. Recently, cytokine profiles have gained attention as potential predictors of HIV incidence due to their involvement in immune regulation and inflammation, presenting new opportunities to enhance preventative strategies. However, the high-dimensional, time-varying nature of cytokine data collected in clinical research, presents challenges for traditional statistical methods like the Cox proportional hazards (PH) model to effectively analyze survival data related to HIV. Machine learning (ML) survival models offer a robust alternative, especially for addressing the limitations of the PH model's assumptions. In this study, we applied survival support vector machine (SSVM) and random survival forest (RSF) models using changes or means in cytokine levels as predictors to assess their association with HIV incidence, evaluate variable importance, measure predictive accuracy using the concordance index (C-index) and integrated Brier score (IBS) and interpret the model's predictions using Shapley additive explanations (SHAP) values. Our results indicated that RSFs models outperformed SSVMs models, with the difference covariate model performing better than the mean covariate model. The highest C-index for SSVM was 0.7180 under the difference covariate model, while for RSF, it reached 0.8801 under the difference covariate model using the log-rank split rule. Key cytokines identified as positive predictors of HIV incidence included TNF-A, BASIC-FGF, IL-5, MCP-3, and EOTAXIN, while 29 cytokines were negative predictors. Baseline factors such as condom use frequency, treatment status, number of partners, and sexual activity also emerged as significant predictors. This study underscored the potential of cytokine profiles for predicting HIV incidence and highlighted the advantages of RSFs models in analyzing high-dimensional, time-varying data over SSVMs. It further through ablation studies emphasized the importance of selecting key features within mean and difference based covariate models to achieve an optimal balance between model complexity and predictive accuracy.

Indexed as

CytokinesHIV InfectionsMachine LearningAdultFemaleHumansIncidenceMaleProportional Hazards ModelsSupport Vector MachineCytokinesC-indexCytokine profilesHIV incidenceIntegrated Brier scoreRandom survival forestSHAP valuesSurvival support vector machine

Identifiers

PMID39622992
PMCPMC11612445

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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.