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      A Neurometabolic Pattern of Elevated Myo-Inositol in Children Who Are HIV-Exposed and Uninfected: A South African Birth Cohort Study

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          Abstract

          Introduction

          Exposure to maternal HIV in pregnancy may be a risk factor for impaired child neurodevelopment during the first years of life. Altered neurometabolites have been associated with HIV exposure in older children and may help explain the mechanisms underlying this risk. For the first time, we explored neurometabolic profiles of children who are HIV-exposed and uninfected (CHEU) compared to children who are HIV-unexposed (CHU) at 2-3 years of age.

          Methods

          The South African Drakenstein Child Health Study enrolled women during pregnancy and is following mother-child pairs through childhood. MRI scans were acquired on a sub-group of children at 2-3 years. We used single voxel magnetic resonance spectroscopy to measure brain metabolite ratios to total creatine in the parietal grey matter, and left and right parietal white matter of 83 children (36 CHEU; 47 CHU). Using factor analysis, we explored brain metabolite patterns in predefined parietal voxels in these groups using logistic regression models. Differences in relative concentrations of individual metabolites (n-acetyl-aspartate, myo-inositol, total choline, and glutamate) to total creatine between CHEU and CHU groups were also examined.

          Results

          Factor analysis revealed four different metabolite patterns, each one characterized by covarying ratios of a single metabolite in parietal grey and white matter. The cross-regional pattern dominated by myo-inositol, a marker for glial reactivity and inflammation, was associated with HIV exposure status (OR 1.63; 95% CI 1.11–2.50) which held after adjusting for child age, sex, and maternal alcohol use during pregnancy (OR 1.59; 95% CI 1.07 –2.47). Additionally, higher relative concentrations of myo-inositol to total creatine were found in left and right parietal white matter of CHEU compared to CHU (p=0.025 and p=0.001 respectively).

          Discussion

          Increased ratios of myo-inositol to total creatine in parietal brain regions at age 2-3 years in CHEU are suggestive of early and ongoing neuroinflammatory processes. Altered relative concentrations of neurometabolites were found predominantly in the white matter, which is sensitive to neuroinflammation, and may contribute to developmental risk in this population. Future work on the trajectory of myo-inositol over time in CHEU, alongside markers of neurocognitive development, and the potential for specific neurodevelopmental interventions will be useful.

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          Most cited references64

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          Early childhood development coming of age: science through the life course

          Early childhood development programmes vary in coordination and quality, with inadequate and inequitable access, especially for children younger than 3 years. New estimates, based on proxy measures of stunting and poverty, indicate that 250 million children (43%) younger than 5 years in low-income and middle-income countries are at risk of not reaching their developmental potential. There is therefore an urgent need to increase multisectoral coverage of quality programming that incorporates health, nutrition, security and safety, responsive caregiving, and early learning. Equitable early childhood policies and programmes are crucial for meeting Sustainable Development Goals, and for children to develop the intellectual skills, creativity, and wellbeing required to become healthy and productive adults. In this paper, the first in a three part Series on early childhood development, we examine recent scientific progress and global commitments to early childhood development. Research, programmes, and policies have advanced substantially since 2000, with new neuroscientific evidence linking early adversity and nurturing care with brain development and function throughout the life course.
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            Inflammation and its discontents: the role of cytokines in the pathophysiology of major depression.

            Recognition that inflammation may represent a common mechanism of disease has been extended to include neuropsychiatric disorders including major depression. Patients with major depression have been found to exhibit increased peripheral blood inflammatory biomarkers, including inflammatory cytokines, which have been shown to access the brain and interact with virtually every pathophysiologic domain known to be involved in depression, including neurotransmitter metabolism, neuroendocrine function, and neural plasticity. Indeed, activation of inflammatory pathways within the brain is believed to contribute to a confluence of decreased neurotrophic support and altered glutamate release/reuptake, as well as oxidative stress, leading to excitotoxicity and loss of glial elements, consistent with neuropathologic findings that characterize depressive disorders. Further instantiating the link between inflammation and depression are data demonstrating that psychosocial stress, a well-known precipitant of mood disorders, is capable of stimulating inflammatory signaling molecules, including nuclear factor kappa B, in part, through activation of sympathetic nervous system outflow pathways. Interestingly, depressed patients with increased inflammatory biomarkers have been found to be more likely to exhibit treatment resistance, and in several studies, antidepressant therapy has been associated with decreased inflammatory responses. Finally, preliminary data from patients with inflammatory disorders, as well as medically healthy depressed patients, suggest that inhibiting proinflammatory cytokines or their signaling pathways may improve depressed mood and increase treatment response to conventional antidepressant medication. Translational implications of these findings include the unique opportunity to identify relevant patient populations, apply immune-targeted therapies, and monitor therapeutic efficacy at the level of the immune system in addition to behavior.
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              Raincloud plots: a multi-platform tool for robust data visualization

              Across scientific disciplines, there is a rapidly growing recognition of the need for more statistically robust, transparent approaches to data visualization. Complementary to this, many scientists have called for plotting tools that accurately and transparently convey key aspects of statistical effects and raw data with minimal distortion. Previously common approaches, such as plotting conditional mean or median barplots together with error-bars have been criticized for distorting effect size, hiding underlying patterns in the raw data, and obscuring the assumptions upon which the most commonly used statistical tests are based. Here we describe a data visualization approach which overcomes these issues, providing maximal statistical information while preserving the desired ‘inference at a glance’ nature of barplots and other similar visualization devices. These “raincloud plots” can visualize raw data, probability density, and key summary statistics such as median, mean, and relevant confidence intervals in an appealing and flexible format with minimal redundancy. In this tutorial paper, we provide basic demonstrations of the strength of raincloud plots and similar approaches, outline potential modifications for their optimal use, and provide open-source code for their streamlined implementation in R, Python and Matlab ( https://github.com/RainCloudPlots/RainCloudPlots). Readers can investigate the R and Python tutorials interactively in the browser using Binder by Project Jupyter.
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                Author and article information

                Contributors
                Journal
                Front Immunol
                Front Immunol
                Front. Immunol.
                Frontiers in Immunology
                Frontiers Media S.A.
                1664-3224
                28 March 2022
                2022
                : 13
                : 800273
                Affiliations
                [1] 1 Department of Paediatrics and Child Health, Red Cross War Memorial Children’s Hospital, University of Cape Town , Cape Town, South Africa
                [2] 2 Research Master Brain and Cognitive Sciences, Faculty of Science, University of Amsterdam , Amsterdam, Netherlands
                [3] 3 Department of Clinical Research, London School of Hygiene & Tropical Medicine , London, United Kingdom
                [4] 4 Neuroscience Institute, University of Cape Town , Cape Town, South Africa
                [5] 5 Department of Human Biology, University of Cape Town , Cape Town, South Africa
                [6] 6 Cape Universities Body Imaging Centre (CUBIC) , Cape Town, South Africa
                [7] 7 Departments of Neurology, Psychiatry and Biobehavioral Sciences, University of California, Los Angeles , Los Angeles, CA, United States
                [8] 8 SAMRC Unit on Risk and Resilience in Mental Disorders, Stellenbosch University , Cape Town, South Africa
                [9] 9 MRC International Statistics & Epidemiology Group, London School of Hygiene & Tropical Medicine , London, United Kingdom
                [10] 10 Department of Psychiatry and Mental Health, University of Cape Town , Cape Town, South Africa
                [11] 11 SAMRC Unit on Child & Adolescent Health, University of Cape Town , Cape Town, South Africa
                [12] 12 SAMRC Unit on Risk and Resilience in Mental Disorders, University of Cape Town , Cape Town, South Africa
                Author notes

                Edited by: Richard Idro, Makerere University, Uganda

                Reviewed by: Michelle Coleman, Seattle Children’s Research Institute, United States; Charles Gasparovic, University of New Mexico, United States; Kim M. Cecil, Cincinnati Children’s Hospital Medical Center, United States

                *Correspondence: Catherine J. Wedderburn, catherine.wedderburn@ 123456uct.ac.za

                †These authors share first authorship

                ‡These authors share last authorship

                This article was submitted to Multiple Sclerosis and Neuroimmunology, a section of the journal Frontiers in Immunology

                Article
                10.3389/fimmu.2022.800273
                8995436
                35419007
                2dd908c5-7d6b-4b20-9762-7db7d2abe4db
                Copyright © 2022 Bertran-Cobo, Wedderburn, Robertson, Subramoney, Narr, Joshi, Roos, Rehman, Hoffman, Zar, Stein and Donald

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 22 October 2021
                : 22 February 2022
                Page count
                Figures: 3, Tables: 4, Equations: 0, References: 67, Pages: 14, Words: 7345
                Funding
                Funded by: Bill and Melinda Gates Foundation , doi 10.13039/100000865;
                Award ID: OPP 1017641
                Funded by: Wellcome Trust , doi 10.13039/100010269;
                Award ID: 203525/Z/16/Z
                Funded by: National Institute on Alcohol Abuse and Alcoholism , doi 10.13039/100000027;
                Award ID: R21AA023887
                Funded by: Academy of Medical Sciences , doi 10.13039/501100000691;
                Award ID: NAF002/1001
                Funded by: Brain and Behavior Research Foundation , doi 10.13039/100000874;
                Award ID: 24467
                Funded by: South African Medical Research Council , doi 10.13039/501100001322;
                Funded by: Medical Research Council , doi 10.13039/501100000265;
                Funded by: National Research Foundation , doi 10.13039/501100001321;
                Funded by: National Institutes of Health , doi 10.13039/100000002;
                Categories
                Immunology
                Original Research

                Immunology
                hiv exposure,magnetic resonance spectroscopy,neuroinflammation,brain development,myo-inositol

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