Thursday, June 11, 2020

Can your gut microbes tell you how old you really are?


Highlights:
    In 2018 scientists from Gladyshev lab specializing in aging research started a collaboration with Insilico Medicine resulting in a widely-publicized proof of concept microbiomic aging clock ; The clock has been validated on multiple independent data sets;
    The clock was shown to be biologically-relevant and used to demonstrate that diabetic patients look older than their chronological age;
    The study was published in iScience and is expected to be used in new data analysis tools for COVID-19 and longevity research;
June 11th, 2020 - Recent advances in deep learning have allowed AI algorithms to outperform humans in image, text, and voice recognition. One particular use for AI in biology is deep aging clocks. Deep aging clocks are trained on large samples to predict human biological age using different data types, such as: pictures, videos, voice, blood biochemistry, gene and protein expression, and MRI. In a study recently published in iScience, Harvard and Insilico Medicine scientists used thousands of whole genome sequencing samples from gut bacteria to develop and validate a new deep microbiomic aging clock. This new tool indicates that the age of the host is a significant contributor to the gut community dynamics.

Over the last decade human gut microbiome studies have produced multiple surprising results. The bacteria in our gut are now known to be major contributors to the immune function, brain development and activity, central metabolism, obesity pathogenesis and many other processes. The growing realization of the role microbiota plays in human health makes it essential to understand what factors shape gut communities and how to manipulate them.
Such factors include the mode of birth, diet, physical activity and age. The effect age elicits on microflora dynamics is much better understood for the early stages of life. During the first year of life all people are much more similar in terms of diet and behaviour, compared to adults. Consequently, their gut flora goes through clearly defined stages. But upon transitioning to adulthood, multiple confounders such as diet, tobacco and alcohol consumption, and level of physical activity make individual microfloras extremely diverse. The NIH Human Microbiome Project has shown that there is no core community in adult guts, although the various combinations of microbial species tend to have similar functions and metabolic capabilities.

Multiple studies have identified some age-related trends in gut microflora. However, the findings usually have unclear general applicability due to localized sampling. In a joint project between Insilico Medicine and the laboratory of Vadim Gladyshev at Brigham and Women's Hospital and Harvard Medical School, the data from 13 public studies on human gut microbiome were aggregated to explore the possibility of developing an aging clock based on the microflora relative abundance profiles.

The initial attempt to predict chronological age based on gut community species composition was published in BioRxiv in December 2018. Since then the team further improved their approach and recently published their results in the iScience journal. More than 1100 species-level microflora compositions were used to train a Deep Neural Network in a cross-validated manner. The resulting ensemble predicts hosts' age in an independent data set collection with a mean error of 5.9-6.8 years.

The published intestinal age predictor proves that there are microflora succession patterns associated with age progression in the adult. The described workflow can be used to recreate similar models with data from other platforms and explore the effect of specific bacterial taxa on the course of human aging in a more controlled setting. The authors also suggest the ways to identify the microbes with potential to accelerate or slow down aging.
"We are happy to collaborate with the Gladyshev lab on this new microbiomic aging clock, which is the first of its kind. The development of this clock was a long and tedious journey as we originally thought that it would be impossible to build and after the demonstration of the first proof of concept, it took two years to refine and validate. We hope that the demonstrated approach will be used for COVID-19 research and later for longevity research for tracking the effects of different interventions and foods on the predicted intestinal age", said Alex Zhavoronkov, PhD, CEO of Insilico Medicine.
The reported aging clock can be accessed at aging.AI. Insilico Medicine aims to continue developing microbiomic tools and is planning to release COVIDOMIC -- a tool for exploring variables with an effect on the COVID-19 infection outcome, including those derived from patients' respiratory microbiome.

###

Read the original research paper here: https://www.sciencedirect.com/science/article/pii/S2589004220303849

About Insilico Medicine Since 2014 Insilico Medicine is focusing on generative models, reinforcement learning (RL), and other modern machine learning techniques for the generation of new molecular structures with the specified parameters, generation of synthetic biological data, target identification, and prediction of clinical trials outcomes. Recently, Insilico Medicine secured $37 million in series B funding. Since its inception, Insilico Medicine raised over $52 million, published over 80 peer-reviewed papers, applied for over 25 patents, and received multiple industry awards. Website http://insilico.com/.
For further information, images or interviews, please contact: ai@insilico.com.

Tuesday, June 9, 2020

Scientists use machine learning to predict major clinical forms of drug cardiotoxicity

June 9, 2020 - We announce the publication of a new research paper titled 'Dual transcriptomic and molecular machine learning predicts all major clinical forms of drug cardiotoxicity' in Frontiers in Pharmacology. The study was conducted in a collaboration between the Computational Cardiovascular Science Group of the University of Oxford and Insilico Medicine.

'Drug-induced adverse effects on the heart are a very important problem, as highlighted recently in the news regarding COVID-19 treatments. In this study, we are very excited to show how our machine learning algorithm can identify drugs that can cause 6 potential forms of cardiac adverse outcomes from gene expression data', said Professor Blanca Rodriguez.

'Thanks to the increasing power of computers and algorithms to learn, this work represents an exemplar of how AI will revolutionise the future of drug development and safety evaluation in the pharma industry. It extends previous efforts in the field to predict not only the likelihood of a drug to induce lethal arrhythmias, but all the main cardiac adverse events associated with drug action. It also establishes the need for stringent testing criteria for the effective application of AI to this critical domain of the life sciences', said Professor Alfonso Bueno-Orovio.

Computational methods can increase the productivity of drug discovery pipelines, through overcoming challenges such as cardiotoxicity identification. In this paper, researchers demonstrated the simultaneous prediction of cardiotoxic relationships for six drug-induced cardiotoxicity types using a machine learning approach on a large collected and curated dataset of transcriptional and molecular profiles. The algorithm generality is demonstrated through validation in an independent drug dataset, in addition to cross-validation.

Alex Zhavoronkov, founder and CEO of Insilico Medicine comments, 'Drug-induced cardiotoxicity is one of the reasons for late-stage clinical trial failures. We see the Rodriguez group at Oxford as the world's main source of accurate cardiotoxicity predictors. The results of their work are adopted by the FDA, and many pharmaceutical companies. We are very happy to collaborate on AI-powered multi-omics cardiotoxicity prediction engines, and have one of our top AI scientists, Polina Mamoshina, defend her doctorate under one of the biggest names in computational biomedicine'.

Polina Mamoshina, is now Senior Research Scientist at Insilico Medicine. She comments, 'In silico or computational models have made great progress in past years. And one of their great features is that they can be humanized and so have increased chances for translation into drug discovery and development pipelines. The scope of this work was to predict drug adverse reactions that were shown in humans. We believe that this work can be extended to side effects manifested in other organs and tissues and that pipeline that we proposed provides a valuable benchmark for future studies'.

###

Read the original research paper here: https://ora.ox.ac.uk/objects/uuid:2b143ed7-9630-4802-b707-9fb226203384?fbclid=IwAR2bzf3SdQVSzGge3PeB4DBkzSqU55wK4tDRcaTNmvMoNjg5izuNd_dkiFU
 
Media Contact
 
For further information, images or interviews, please contact: ai@insilico.com

About Insilico Medicine
 
Since 2014 Insilico Medicine is focusing on generative models, reinforcement learning (RL), and other modern machine learning techniques for the generation of new molecular structures with the specified parameters, generation of synthetic biological data, target identification, and prediction of clinical trials outcomes. Since its inception, Insilico Medicine raised over $52 million, published over 70 peer-reviewed papers, applied for over 20 patents, and received multiple industry awards. Website http://insilico.com/