Understanding in vivo modelling of depression
dc.contributor.advisor
MacLeod, Malcolm
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dc.contributor.advisor
Wegener, Gregers
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dc.contributor.author
Bannach-Brown, Alexandra
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dc.date.accessioned
2019-10-14T10:28:56Z
dc.date.available
2019-10-14T10:28:56Z
dc.date.issued
2019-11-25
dc.description.abstract
Major Depressive Disorder (MDD) is the leading source of disability globally.
Treatment-resistance among patients is common and even effective pharmacological
therapies have a delayed effect on symptom relief. Better understanding of the
mechanisms underlying depression and the search for potential effective and novel
therapeutic targets are high research and healthcare priorities. Animal models are
commonly used to mimic aspects of the phenotype of the human disorder to
characterise candidate antidepressant agents. Despite these tools, no new
pharmacological interventions have been discovered in the last decade and no
reliable biomarkers have been identified for clinical use.
Systematically reviewing the literature on animal models of depression may provide
an overview of our current understanding of the underlying biological mechanisms
and why no new therapies have been effectively translated to clinic. This field of
research is large, and over 70,000 potentially relevant articles were identified in 2016.
Therefore systematically reviewing this literature presents challenges for human
resources. To combat these challenges, the following contributions to the field have
been made: (1) the novel application of machine learning techniques to identify errors
in human systematic review citation screening; and (2), the novel application of
regular expression dictionaries to large corpuses of preclinical animal literature to help
cluster publications into the disease model investigated and drug intervention tested.
These tools have been applied for systematic review and meta-analysis methodology
to the field of animal models of depression.
All literature on animal models of depression has been systematically identified using
searches carried out in PubMed and EMBASE in May 2016. This literature has been
screened with the help of machine learning classification algorithms, based on a
random set of dual human screened records (5749 records). This achieved a
sensitivity of 98.7% and a specificity of 86% as assessed on in an independent
validation dataset.
Machine learning has been used to identify human screening errors in the set of
documents used to train the algorithm. Correction of these errors with further human
intervention, sees an improvement in specificity to 88.3%. These algorithms allow
irrelevant documents to be automatically removed, reducing the corpus to 18,407
articles that highly likely to be relevant to the research area of animal models of
depression. Custom-made regular expression dictionaries of (1) techniques to induce
depressive-like phenotypes in animals, and (2) known antidepressants have been
curated. The text-mining dictionaries for anti-depressant drugs and commonly used
methods of model induction have been applied to categorise and visualise this large
corpus of records to allow prioritisation of sub-topics of depression for further in depth
systematic review and meta-analyses. These machine-assisted tools for systematic
review methodology are available free to use, online.
Systematic review and meta-analysis has been conducted on two sub-topics of the
literature on animal models of depression. Firstly, the literature on the effects of
ketamine as an anti-depressant in animal models of depression has been
summarised with systematic review techniques and the effects of ketamine on
depressive-like behaviour in the forced swim test, has been pooled using meta-analysis.
The timing of administration of ketamine relative to the outcome assessment
was significantly associated with decreases in effect size. This meta-analysis
revealed no statistically significant heterogeneity between the studies. Secondly, the
literature on use of gut microbial altering interventions to induce and treat depressive-like
phenotypes in animal models of depression has been summarised and their
effects have been pooled across studies using meta-analysis. The systematic review
and meta-analysis of microbiota interventions identified a broad range of outcomes
investigated in the primary literature and several probiotic treatments to reduce
depressive-like behaviour were investigate gaps in the literature. Finally, a primary
hypothesis-confirming animal experiment, where measures to reduce the risk of bias
have been implemented was carried out to investigate the effects of prebiotics on
depressive- and anxiety-like behaviour in a genetic animal model of depression, the
Flinders Sensitive Line (FSL) rats.
Online tools have been developed to provide an overview of animal models of
depression and anti-depressant drugs investigated in the literature, using systematic
review methodology and automation tools. This thesis reports meta-analyses on two
sub-topics within animal models of depression; the effect of microbiota interventions,
and the effects of ketamine; along with a primary animal experiment to test the effects of prebiotics on depressive-like behaviour in a genetic rodent model of depression.
en
dc.identifier.uri
http://hdl.handle.net/1842/36223
dc.language.iso
en
dc.publisher
The University of Edinburgh
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dc.relation.hasversion
Bahor, Z., Liao, J., Macleod, M.R., Bannach-Brown, A., McCann, S.K., Wever, K.E., Thomas, J., Ottavi, T., Howells, D.W., Rice, A. and Ananiadou, S., 2017. Risk of bias reporting in the recent animal focal cerebral ischaemia literature. Clinical Science, 131(20), pp.2525-2532.
en
dc.relation.hasversion
Bannach-Brown, A., Liao, J., Wegener, G., Macleod, M. R., 2016. Understanding in vivo modelling of depression: a systematic review protocol. CAMARADES repository of protocols. Retrieved from: https://drive.google.com/file/d/0BxckMffc78BYLWM2QUpBY3l1Q1k/view
en
dc.relation.hasversion
Bannach-Brown, A., Thomas, J., Przybyła, P., Liao, J., (2016). “Protocol for Error Analysis: Machine learning and text mining solutions for systematic reviews of animal models of depression”. Published on CAMARADES Website. www.CAMARADES.info. Direct Access: https://drive.google.com/file/d/0BxckMffc78BYTm0tUzJJZkc1alk/view
en
dc.relation.hasversion
Bannach-Brown, A., Przybyła, P., Thomas, J., Rice, A.S., Ananiadou, S., Liao, J. and Macleod, M.R., 2018. The use of text-mining and machine learning algorithms in systematic reviews: reducing workload in preclinical biomedical sciences and reducing human screening error. bioRxiv, p.255760.
en
dc.relation.hasversion
Wang, Q., Liao, J., Hair, K., Bannach-Brown, A., Bahor, Z., Currie, G.L., McCann, S.K., Howells, D.W., Sena, E.S. and Macleod, M.R., 2018. Estimating the statistical performance of different approaches to meta-analysis of data from animal studies in identifying the impact of aspects of study design. bioRxiv, p.256776.
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dc.subject
systematic review
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dc.subject
Major Depressive Disorder
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dc.subject
depression
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dc.subject
meta-analysis
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dc.subject
microbiome-targeting interventions
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dc.title
Understanding in vivo modelling of depression
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dc.type
Thesis or Dissertation
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dc.type.qualificationlevel
Doctoral
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dc.type.qualificationname
PhD Doctor of Philosophy
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