Evidence map›Paper›PMID 32216755›Full record

ArticleBMC infectious diseases2020

Modelling of viral load dynamics and CD4 cell count progression in an antiretroviral naive cohort: using a joint linear mixed and multistate Markov model.

Zelalem G Dessie, Temesgen Zewotir, Henry Mwambi, Delia North

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Article in BMC infectious diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
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17citing papers in PubMed, 1 pooled it
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1 · What the graph read from it

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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

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3 · Its place in the literature

Who cites it

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

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  14. Development of algorithms to estimate EQ-5D and derive health utilities from WHOQOL-HIV Bref: a mapping study.Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation · 2020
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors.

Zelalem G DessieSchool of Mathematics, Statistics and Computer Science, University of KwaZulu-Natal, Durban, South Africa. zelalem_getahune@yahoo.com.
Temesgen ZewotirSchool of Mathematics, Statistics and Computer Science, University of KwaZulu-Natal, Durban, South Africa.
Henry MwambiSchool of Mathematics, Statistics and Computer Science, University of KwaZulu-Natal, Durban, South Africa.
Delia NorthSchool of Mathematics, Statistics and Computer Science, University of KwaZulu-Natal, Durban, South Africa.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPatients infected with HIV may experience a succession of clinical stages before the disease diagnosis and their health status may be followed-up by tracking disease biomarkers. In this study, we present a joint multistate model for predicting the clinical progression of HIV infection which takes into account the viral load and CD4 count biomarkers.

methodsThe data is from an ongoing prospective cohort study conducted among antiretroviral treatment (ART) naïve HIV-infected women in the province of KwaZulu-Natal, South Africa. We presented a joint model that consists of two related submodels: a Markov multistate model for CD4 cell count transitions and a linear mixed effect model for longitudinal viral load dynamics.

resultsViral load dynamics significantly affect the transition intensities of HIV/AIDS disease progression. The analysis also showed that patients with relatively high educational levels (β = - 0.004; 95% confidence interval [CI]:-0.207, - 0.064), high RBC indices scores (β = - 0.01; 95%CI:-0.017, - 0.002) and high physical health scores (β = - 0.001; 95%CI:-0.026, - 0.003) were significantly were associated with a lower rate of viral load increase over time. Patients with TB co-infection (β = 0.002; 95%CI:0.001, 0.004), having many sex partners (β = 0.007; 95%CI:0.003, 0.011), being younger age (β = 0.008; 95%CI:0.003, 0.012) and high liver abnormality scores (β = 0.004; 95%CI:0.001, 0.01) were associated with a higher rate of viral load increase over time. Moreover, patients with many sex partners (β = - 0.61; 95%CI:-0.94, - 0.28) and with a high liver abnormality score (β = - 0.17; 95%CI:-0.30, - 0.05) showed significantly reduced intensities of immunological recovery transitions. Furthermore, a high weight, high education levels, high QoL scores, high RBC parameters and being of middle age significantly increased the intensities of immunological recovery transitions.

conclusionOverall, from a clinical perspective, QoL measurement items, being of a younger age, clinical attributes, marital status, and educational status are associated with the current state of the patient, and are an important contributing factor to extend survival of the patients and guide clinical interventions. From a methodological perspective, it can be concluded that a joint multistate model approach provides wide-ranging information about the progression and assists to provide specific dynamic predictions and increasingly precise knowledge of diseases.

Indexed as

Markov ChainsModels, StatisticalAcquired Immunodeficiency SyndromeAdultAnti-Retroviral AgentsCD4 Lymphocyte CountFactor Analysis, StatisticalFemaleHIVHumansLongitudinal StudiesProspective StudiesQuality of LifeRisk-TakingSouth AfricaViral LoadAnti-Retroviral AgentsFactor analysisLatent variablesMixed effect modelMultistate modelQuality of life

Identifiers

PMID32216755
PMCPMC7098156

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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.