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<?covid-19-tdm?>
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  <front>
    <journal-meta>
      <journal-id journal-id-type="publisher-id">JMIR</journal-id>
      <journal-id journal-id-type="nlm-ta">J Med Internet Res</journal-id>
      <journal-title>Journal of Medical Internet Research</journal-title>
      <issn pub-type="epub">1438-8871</issn>
      <publisher>
        <publisher-name>JMIR Publications</publisher-name>
        <publisher-loc>Toronto, Canada</publisher-loc>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="publisher-id">v23i3e22453</article-id>
      <article-id pub-id-type="pmid">33560998</article-id>
      <article-id pub-id-type="doi">10.2196/22453</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Viewpoint</subject>
        </subj-group>
        <subj-group subj-group-type="article-type">
          <subject>Viewpoint</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Artificial Intelligence–Aided Precision Medicine for COVID-19: Strategic Areas of Research and Development</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="editor">
          <name>
            <surname>Eysenbach</surname>
            <given-names>Gunther</given-names>
          </name>
        </contrib>
        <contrib contrib-type="editor">
          <name>
            <surname>Basch</surname>
            <given-names>Corey</given-names>
          </name>
        </contrib>
      </contrib-group>
      <contrib-group>
        <contrib contrib-type="reviewer">
          <name>
            <surname>Ferrini</surname>
            <given-names>Krizia</given-names>
          </name>
        </contrib>
        <contrib contrib-type="reviewer">
          <name>
            <surname>Afzal</surname>
            <given-names>Muhammad</given-names>
          </name>
        </contrib>
      </contrib-group>
      <contrib-group>
        <contrib id="contrib1" contrib-type="author">
          <name name-style="western">
            <surname>Santus</surname>
            <given-names>Enrico</given-names>
          </name>
          <degrees>PhD</degrees>
          <xref rid="aff01" ref-type="aff">1</xref>
          <xref rid="aff02" ref-type="aff">2</xref>
          <ext-link ext-link-type="orcid">https://orcid.org/0000-0002-7327-2731</ext-link>
        </contrib>
        <contrib id="contrib2" contrib-type="author">
          <name name-style="western">
            <surname>Marino</surname>
            <given-names>Nicola</given-names>
          </name>
          <degrees>BSc</degrees>
          <xref rid="aff02" ref-type="aff">2</xref>
          <xref rid="aff03" ref-type="aff">3</xref>
          <ext-link ext-link-type="orcid">https://orcid.org/0000-0001-7510-1939</ext-link>
        </contrib>
        <contrib id="contrib3" contrib-type="author" corresp="yes">
          <name name-style="western">
            <surname>Cirillo</surname>
            <given-names>Davide</given-names>
          </name>
          <degrees>PhD</degrees>
          <xref rid="aff02" ref-type="aff">2</xref>
          <xref rid="aff04" ref-type="aff">4</xref>
          <address>
            <institution>Barcelona Supercomputing Center</institution>
            <addr-line>c/Jordi Girona, 29</addr-line>
            <addr-line>Barcelona</addr-line>
            <country>Spain</country>
            <phone>34 934137971</phone>
            <email>davide.cirillo@bsc.es</email>
          </address>
          <ext-link ext-link-type="orcid">https://orcid.org/0000-0003-4982-4716</ext-link>
        </contrib>
        <contrib id="contrib4" contrib-type="author">
          <name name-style="western">
            <surname>Chersoni</surname>
            <given-names>Emmanuele</given-names>
          </name>
          <degrees>PhD</degrees>
          <xref rid="aff05" ref-type="aff">5</xref>
          <ext-link ext-link-type="orcid">https://orcid.org/0000-0001-8742-0451</ext-link>
        </contrib>
        <contrib id="contrib5" contrib-type="author">
          <name name-style="western">
            <surname>Montagud</surname>
            <given-names>Arnau</given-names>
          </name>
          <degrees>PhD</degrees>
          <xref rid="aff04" ref-type="aff">4</xref>
          <ext-link ext-link-type="orcid">https://orcid.org/0000-0002-7696-1241</ext-link>
        </contrib>
        <contrib id="contrib6" contrib-type="author">
          <name name-style="western">
            <surname>Santuccione Chadha</surname>
            <given-names>Antonella</given-names>
          </name>
          <degrees>MD</degrees>
          <xref rid="aff02" ref-type="aff">2</xref>
          <xref rid="aff06" ref-type="aff">6</xref>
          <ext-link ext-link-type="orcid">https://orcid.org/0000-0002-4021-3129</ext-link>
        </contrib>
        <contrib id="contrib7" contrib-type="author">
          <name name-style="western">
            <surname>Valencia</surname>
            <given-names>Alfonso</given-names>
          </name>
          <degrees>PhD</degrees>
          <xref rid="aff04" ref-type="aff">4</xref>
          <xref rid="aff07" ref-type="aff">7</xref>
          <ext-link ext-link-type="orcid">https://orcid.org/0000-0002-8937-6789</ext-link>
        </contrib>
        <contrib id="contrib8" contrib-type="author">
          <name name-style="western">
            <surname>Hughes</surname>
            <given-names>Kevin</given-names>
          </name>
          <degrees>MD</degrees>
          <xref rid="aff08" ref-type="aff">8</xref>
          <ext-link ext-link-type="orcid">https://orcid.org/0000-0003-4084-6484</ext-link>
        </contrib>
        <contrib id="contrib9" contrib-type="author">
          <name name-style="western">
            <surname>Lindvall</surname>
            <given-names>Charlotta</given-names>
          </name>
          <degrees>MD, PhD</degrees>
          <xref rid="aff09" ref-type="aff">9</xref>
          <xref rid="aff10" ref-type="aff">10</xref>
          <ext-link ext-link-type="orcid">https://orcid.org/0000-0003-2090-2039</ext-link>
        </contrib>
      </contrib-group>
      <aff id="aff01">
        <label>1</label>
        <institution>Division of Decision Science and Advanced Analytics</institution>
        <institution>Bayer Pharmaceuticals</institution>
        <addr-line>Whippany, NJ</addr-line>
        <country>United States</country>
      </aff>
      <aff id="aff02">
        <label>2</label>
        <institution>The Women's Brain Project</institution>
        <addr-line>Zurich</addr-line>
        <country>Switzerland</country>
      </aff>
      <aff id="aff03">
        <label>3</label>
        <institution>Department of Medical and Surgical Sciences</institution>
        <institution>Università degli Studi di Foggia</institution>
        <addr-line>Foggia</addr-line>
        <country>Italy</country>
      </aff>
      <aff id="aff04">
        <label>4</label>
        <institution>Barcelona Supercomputing Center</institution>
        <addr-line>Barcelona</addr-line>
        <country>Spain</country>
      </aff>
      <aff id="aff05">
        <label>5</label>
        <institution>Department of Chinese and Bilingual Studies</institution>
        <institution>The Hong Kong Polytechnic University</institution>
        <addr-line>Hong Kong</addr-line>
        <country>China (Hong Kong)</country>
      </aff>
      <aff id="aff06">
        <label>6</label>
        <institution>Biogen International GmbH</institution>
        <addr-line>Baar</addr-line>
        <country>Switzerland</country>
      </aff>
      <aff id="aff07">
        <label>7</label>
        <institution>Institució Catalana de Recerca i Estudis Avançats</institution>
        <addr-line>Barcelona</addr-line>
        <country>Spain</country>
      </aff>
      <aff id="aff08">
        <label>8</label>
        <institution>Massachusetts General Hospital</institution>
        <addr-line>Boston, MA</addr-line>
        <country>United States</country>
      </aff>
      <aff id="aff09">
        <label>9</label>
        <institution>Dana-Farber Cancer Institute</institution>
        <addr-line>Boston, MA</addr-line>
        <country>United States</country>
      </aff>
      <aff id="aff10">
        <label>10</label>
        <institution>Harvard Medical School</institution>
        <addr-line>Boston, MA</addr-line>
        <country>United States</country>
      </aff>
      <author-notes>
        <corresp>Corresponding Author: Davide Cirillo <email>davide.cirillo@bsc.es</email></corresp>
      </author-notes>
      <pub-date pub-type="collection">
        <month>3</month>
        <year>2021</year>
      </pub-date>
      <pub-date pub-type="epub">
        <day>12</day>
        <month>3</month>
        <year>2021</year>
      </pub-date>
      <volume>23</volume>
      <issue>3</issue>
      <elocation-id>e22453</elocation-id>
      <history>
        <date date-type="received">
          <day>12</day>
          <month>7</month>
          <year>2020</year>
        </date>
        <date date-type="rev-request">
          <day>17</day>
          <month>8</month>
          <year>2020</year>
        </date>
        <date date-type="rev-recd">
          <day>7</day>
          <month>10</month>
          <year>2020</year>
        </date>
        <date date-type="accepted">
          <day>31</day>
          <month>1</month>
          <year>2021</year>
        </date>
      </history>
      <copyright-statement>©Enrico Santus, Nicola Marino, Davide Cirillo, Emmanuele Chersoni, Arnau Montagud, Antonella Santuccione Chadha, Alfonso Valencia, Kevin Hughes, Charlotta Lindvall. Originally published in the Journal of Medical Internet Research (http://www.jmir.org), 12.03.2021.</copyright-statement>
      <copyright-year>2021</copyright-year>
      <license license-type="open-access" xlink:href="https://creativecommons.org/licenses/by/4.0/">
        <p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in the Journal of Medical Internet Research, is properly cited. The complete bibliographic information, a link to the original publication on http://www.jmir.org/, as well as this copyright and license information must be included.</p>
      </license>
      <self-uri xlink:href="https://www.jmir.org/2021/3/e22453" xlink:type="simple"/>
      <abstract>
        <p>Artificial intelligence (AI) technologies can play a key role in preventing, detecting, and monitoring epidemics. In this paper, we provide an overview of the recently published literature on the COVID-19 pandemic in four strategic areas: (1) triage, diagnosis, and risk prediction; (2) drug repurposing and development; (3) pharmacogenomics and vaccines; and (4) mining of the medical literature. We highlight how AI-powered health care can enable public health systems to efficiently handle future outbreaks and improve patient outcomes.</p>
      </abstract>
      <kwd-group>
        <kwd>COVID-19</kwd>
        <kwd>SARS-CoV-2</kwd>
        <kwd>artificial intelligence</kwd>
        <kwd>personalized medicine</kwd>
        <kwd>precision medicine</kwd>
        <kwd>prevention</kwd>
        <kwd>monitoring</kwd>
        <kwd>epidemic</kwd>
        <kwd>literature</kwd>
        <kwd>public health</kwd>
        <kwd>pandemic</kwd>
      </kwd-group>
    </article-meta>
  </front>
  <body>
    <sec sec-type="introduction">
      <title>Introduction</title>
      <p>The ongoing COVID-19 pandemic has highlighted the fragility of the health care system during unexpected events, testing the endurance of even the top-performing ones [<xref ref-type="bibr" rid="ref1">1</xref>]. As noted by several scholars, embracing artificial intelligence (AI) for health care optimization and outcome improvement is not an option anymore [<xref ref-type="bibr" rid="ref2">2</xref>]. Concerning the ongoing COVID-19 pandemic, several studies have highlighted that the timely inclusion of AI-powered technologies would have accelerated the identification of and effective response to COVID-19 outbreaks worldwide. An example is the widely reported algorithm from the Canadian company BlueDot, based on natural language processing (NLP) and machine learning, which forecasted the emerging risk of a virus spread in Hubei province in late December 2019, by screening news reports and airline ticketing [<xref ref-type="bibr" rid="ref3">3</xref>].</p>
      <p>Awareness of the benefits of employing AI to support and manage the COVID-19 crisis and its aftermath is increasing, particularly in the medical and research community. Notable examples of early AI-powered contributions include the discovery of relevant SARS-CoV-2 target proteins by DeepMind’s AlphaFold [<xref ref-type="bibr" rid="ref4">4</xref>] and the design by Infervision of a computer vision algorithm for the detection of coronavirus pneumonia based on lung images [<xref ref-type="bibr" rid="ref5">5</xref>].</p>
      <p>Benefits do, however, come with technical challenges and related risks that still need to be properly assessed. For example, the absence of transparency and interpretability in AI models obscures the fact that the efficacy of these technologies is not equal across population groups. COVID-19 incidence and outcomes vary according to a large number of individual factors, including age, sex, ethnicity, health status, drug utilization, and others [<xref ref-type="bibr" rid="ref6">6</xref>]. Sensitizing AI technologies to the diversity of the patient population and ensuring data security [<xref ref-type="bibr" rid="ref7">7</xref>] is imperative to avoid biased decisions [<xref ref-type="bibr" rid="ref8">8</xref>-<xref ref-type="bibr" rid="ref10">10</xref>]. Therefore, a crucial step to obtain robust, trustworthy, and intelligible applications that account for demographic equity is to assess potential biases in the resources used to train AI models for precision medicine [<xref ref-type="bibr" rid="ref11">11</xref>].</p>
      <p>As of today, AI systems are, regrettably, rarely endowed with robustness to class imbalances, such as sex and gender groups [<xref ref-type="bibr" rid="ref12">12</xref>]. In this regard, sex differences in COVID-19 cases, as well as sex-specific risk factors and socioeconomic burden, have been recently highlighted in a case study by the European Commission [<xref ref-type="bibr" rid="ref13">13</xref>]. Dataset multidimensionality that can fairly represent the population constitutes one of the main challenges for biobanking and cohort design efforts that collect different axes of health data [<xref ref-type="bibr" rid="ref14">14</xref>]. In this regard, fair and broad data collection systems are of primary importance. Two essential international references for COVID-19 genomic and medical data are the EMBL-EBI COVID-19 Data Portal [<xref ref-type="bibr" rid="ref15">15</xref>] and the NIH National COVID Cohort Collaborative (N3C) [<xref ref-type="bibr" rid="ref16">16</xref>]. The COVID-19 Host Genetics Initiative [<xref ref-type="bibr" rid="ref17">17</xref>] is an international collaborative undertaking to share resources to investigate the genetic determinants of COVID-19 susceptibility, severity, and outcomes [<xref ref-type="bibr" rid="ref18">18</xref>]. The Coronavirus Pandemic Epidemiology (COPE) consortium aims to involve experts in the development of a personalized COVID-19 Symptom Tracker mobile app that works as a real-time data capture platform [<xref ref-type="bibr" rid="ref6">6</xref>], which garnered over 2.8 million users in a few days. Moreover, COVID-19 sex-disaggregated data are collected by Global Health 50/50 [<xref ref-type="bibr" rid="ref19">19</xref>], an initiative housed at University College London, advocating for gender equity.</p>
      <p>Other ethical concerns include life-or-death decisions through risk prediction models, which may help optimize resource allocation in times of scarcity. The application of nonoptimal models may incur the risk of worsening biases and exacerbating disparities for people with serious illnesses and different treatment priorities, potentially causing the reduction in the use of services rather than achieving the best patient care [<xref ref-type="bibr" rid="ref20">20</xref>]. Nevertheless, the power of prediction models is impressive, and it may play a key role in the future if properly exploited. For instance, a study from Cambridge University [<xref ref-type="bibr" rid="ref21">21</xref>] shows how the use of secure AI operating on anonymized COVID-19 data can accurately predict the patient journey, allowing an optimal allocation of resources and enabling well-informed and personalized health care decision-making. This is a particularly important point, especially considering the difficulty in managing the increasing need for intensive care units (ICUs) during the COVID-19 pandemic peak [<xref ref-type="bibr" rid="ref22">22</xref>,<xref ref-type="bibr" rid="ref23">23</xref>].</p>
      <p>The way the AI systems will be exploited is probably the most delicate topic in this adoption process, particularly if we refer to the decisional independence of the medical staff. As humans, in fact, clinicians are also affected by numerous cognitive biases, including the <italic>confirmation bias</italic>, which may lead them to give excessive importance to the evidence supporting automated prediction (eg, risk prediction, diagnosis, and treatment suggestion) and ignore evidence that refutes it [<xref ref-type="bibr" rid="ref8">8</xref>,<xref ref-type="bibr" rid="ref24">24</xref>].</p>
      <p>Despite the abovementioned concerns, there are numerous success stories in the adoption of risk prediction models. For example, Duke University adopted a system called Sepsis Watch that identifies in advance the inflammation leading to sepsis—one of the leading causes of hospital deaths. Within two years from the tool introduction, the number of sepsis-induced patients drastically decreased [<xref ref-type="bibr" rid="ref25">25</xref>], thanks to three key elements: (1) adaptation of the predictive model to a highly specific context; (2) scalability through integration with hospital workflows; and (3) the adopted user experience–based approach, which places clinicians and health care professionals at the center of the software development process, adhering with the human-in-the-loop paradigm [<xref ref-type="bibr" rid="ref26">26</xref>,<xref ref-type="bibr" rid="ref27">27</xref>].</p>
      <p>The COVID-19 crisis is accelerating anticipated changes towards a stronger collaboration between computer science and medicine. In particular, the crisis has exposed the need for increased scrutiny of the relationship between AI and patients as well as health care personnel under the lens of human and emotional needs, as demonstrated by the surge of mental health consequences of the pandemic [<xref ref-type="bibr" rid="ref28">28</xref>] and the growing development of AI-based mental health apps and related digital tools [<xref ref-type="bibr" rid="ref29">29</xref>]. Such aspects, together with others related to general data access and the use of AI for disease outcome prediction, are fueling the current debate about the convergence of AI and medicine [<xref ref-type="bibr" rid="ref30">30</xref>,<xref ref-type="bibr" rid="ref31">31</xref>] and the actionable realization of AI-powered innovations to bridge the gap between technological research and medical practice, including applications in medical triage and advice, diagnostics and risk-adjusted paneling, population health management, and digital devices integration [<xref ref-type="bibr" rid="ref32">32</xref>]. Concerning this aspect, it is important to mention the recent publication of guidelines for the rigorous and transparent adoption of AI in the clinical practice: CONSORT-AI (Consolidated Standards of Reporting Trials–Artificial Intelligence) [<xref ref-type="bibr" rid="ref33">33</xref>] and SPIRIT-AI (Standard Protocol Items: Recommendations for Interventional Trials–Artificial Intelligence) [<xref ref-type="bibr" rid="ref34">34</xref>].</p>
      <p>Translating patient data to successful therapies is the major objective of implementing AI for health [<xref ref-type="bibr" rid="ref35">35</xref>], especially in times of a pandemic crisis, with the ultimate goal of achieving a successful bench-to-bedside model for better clinical decision-making [<xref ref-type="bibr" rid="ref36">36</xref>,<xref ref-type="bibr" rid="ref37">37</xref>]. In this work, we review some major examples of what AI has achieved during the COVID-19 pandemic and the challenges that this technology and the medical community are currently facing in four main strategic areas of research and development (<xref rid="figure1" ref-type="fig">Figure 1</xref>): (1) triage, diagnosis, and risk prediction; (2) drug repurposing and development; (3) pharmacogenomics and vaccines; (4) mining of the medical literature.</p>
      <fig id="figure1" position="float">
        <label>Figure 1</label>
        <caption>
          <p>Main strategic areas of research and development for the realization of artificial intelligence (AI) to fight COVID-19: (1) triage, diagnosis, and risk prediction; (2) drug repurposing and development; (3) pharmacogenomics and vaccines; and (4) mining of the medical literature. The text within the four panels enlists the advantages and actionable solutions exhibited by the AI-aided precision medicine approaches surveyed in this work.</p>
        </caption>
        <graphic xlink:href="jmir_v23i3e22453_fig1.png" alt-version="no" mimetype="image" position="float" xlink:type="simple"/>
      </fig>
    </sec>
    <sec>
      <title>Triage, Diagnosis, and Risk Prediction</title>
      <p>AI has been applied to determine treatment priorities in patients with COVID-19 or triage and to better allocate limited resources. A group of researchers at the General Hospital of the People’s Liberation Army (PLAGH), Beijing, China, has developed an online triage tool model [<xref ref-type="bibr" rid="ref38">38</xref>] to manage suspected COVID-19 pneumonia in adult patients with fever [<xref ref-type="bibr" rid="ref39">39</xref>]. Using clinical symptoms, routine laboratory tests, and other clinical information available at admission (eg, clinical features), they trained a model based on logistic regression with the least absolute shrinkage and selection operator (LASSO), obtaining an area under the receiver operating characteristic curve (AUROC) of 0.841 (100% sensitivity and 72.7% specificity). Based on data from two hospitals in Wenzhou, Zhejiang, China, another study group recently used an entropy-based feature selection approach: they modeled combinations of clinical features that could identify initial presentation patients who are at a higher risk of developing severe illness, with an accuracy of 80% [<xref ref-type="bibr" rid="ref40">40</xref>]. Their results show that mildly elevated alanine aminotransferase levels, the presence of myalgias (body aches), and an elevated hemoglobin level (red blood cells), in this order, are predictive of the later development of acute respiratory distress syndrome.</p>
      <p>A thorough study on risk prediction was carried out at the University of Cambridge based on the development of a proof of concept system to model the full patient journey through risk prediction models [<xref ref-type="bibr" rid="ref21">21</xref>]. By identifying the risk of mortality and ICU/ventilator need, the system aims at enabling doctors to answer questions such as: Which patients are most likely to need ventilators within a week? How many free ICU beds in the hospital are we likely to have in a week from now? Which of two patients will get more benefits from going on a ventilator today? The predictive models showed accuracies ranging from 77% for ventilator need to 83% for ICU admission and 87% for mortality.</p>
      <p>Risk prediction models are not new to the AI-aided health care approach. They have already been successfully utilized for tasks such as predicting the risk of developing cancer [<xref ref-type="bibr" rid="ref41">41</xref>,<xref ref-type="bibr" rid="ref42">42</xref>] and identifying which patients are likely to benefit from heart-related procedures [<xref ref-type="bibr" rid="ref43">43</xref>]. However, the COVID-19 crisis has accelerated the utilization of such models. In a recent study, Wynants and collaborators [<xref ref-type="bibr" rid="ref44">44</xref>] screened 14,217 published titles about the pandemic from PubMed and Embase (Ovid, arXiv, medRxiv, and bioRxiv), finding over 107 studies describing 145 prediction models. Among them, 4 models aimed to identify people at risk and 50, to predict the mortality risk, progression to severe disease, ICU admission, ventilation, intubation, or length of hospital stay. These models not only provide interesting results but also inform about the most valuable predictors, such as age, body temperature, lymphocyte count, and lung imaging features. Despite this, these models cannot be directly applied in the clinical setting without further validation, in order to guarantee data and experiment transparency and robustness, together with decision interpretability and model generalizability.</p>
      <p>The remaining 91 models from this study were dedicated to the diagnosis of COVID-19, 60 of which exploited medical imaging. This number clearly shows that diagnosis is another important field for the application of AI techniques [<xref ref-type="bibr" rid="ref45">45</xref>], with digital pathology exhibiting high effectiveness. In particular, convolutional neural networks (CNNs) have been supporting radiologists in their expert decisions [<xref ref-type="bibr" rid="ref46">46</xref>]. In a recent study, a CNN was trained to automatically learn patterns related to COVID-19 (ie, ground-glass opacities, multifocal patchy consolidation, and/or interstitial changes with a predominantly peripheral distribution), achieving an AUROC of 0.996 (98.2% sensitivity and 92.2% specificity) and outperforming the reverse-transcription polymerase chain reaction, which also suffers from a significant time lag. In addition to accuracy, these approaches put the speed of the diagnosis on the table: CNNs can analyze up to 500 images in a few seconds, whereas radiologists would need hours to complete the same task.</p>
      <p>Although chest computed tomography (CT) scans represent a commonly exploited source of information to train AI to rule out SARS-CoV-2 infection, the rapid detection of patients with COVID-19 can greatly benefit from learning approaches that utilize heterogeneous types of data. In this regard, it is crucial to consider the importance of training CNNs in a correct gender balance in medical imaging datasets to avoid producing distorted classifications for assisted diagnosis [<xref ref-type="bibr" rid="ref12">12</xref>]. Moreover, it is crucial to rely on high-quality benchmarking and robust validation strategies to assess the generalization of the model to other datasets and populations [<xref ref-type="bibr" rid="ref47">47</xref>,<xref ref-type="bibr" rid="ref48">48</xref>].</p>
      <p>Indeed, AI can exploit multidimensional data, including the series of epidemiological, clinical, biological, and radiological criteria defined by the World Health Organization [<xref ref-type="bibr" rid="ref49">49</xref>]. In a collaboration between researchers at hospitals in China and in the USA, CNN and other machine learning methods (eg, support vector machine, random forest, and neural networks) have been used to model and integrate CT scans and clinical information for diagnostic purposes [<xref ref-type="bibr" rid="ref45">45</xref>]. The joint model that uses both information sources achieved a 0.92 AUROC (84.3% sensitivity and 82.8% specificity), outperforming the individual models. Moreover, the models allowed the identification of age, viral exposure, fever, cough, cough with sputum, and white blood cell counts as the main features associated with SARS-CoV-2 infection status.</p>
      <p>Recently, the National Institute of Biomedical Imaging and Bioengineering has launched the Medical Imaging and Data Resource Center with the goal of coupling AI and medical imaging for COVID-19 early detection and personalized therapies [<xref ref-type="bibr" rid="ref50">50</xref>].</p>
      <p>AI has also been utilized to identify patients at higher risk of mortality. Researchers at the Tongji Hospital, Wuhan, China, have screened electronic health records of 375 discharged patients to use clinical measurements as features and have trained a gradient-boosted decision tree model to predict mortality risk [<xref ref-type="bibr" rid="ref51">51</xref>]. The accuracy of the system was 93%. Its utilization would make it possible for physicians to immediately identify critical cases and act accordingly. The model was also able to detect three key clinical features, that is, lactic dehydrogenase, lymphocyte count, and high-sensitivity C-reactive protein.</p>
    </sec>
    <sec>
      <title>Drug Repurposing and Development</title>
      <p>Although triage, diagnosis, and risk prediction are three of the most relevant tasks that AI has helped with during the peaks of the pandemic, other objectives are currently being addressed for long-term solutions. Among them are target selection for drug repurposing [<xref ref-type="bibr" rid="ref52">52</xref>] and approaches for drug development, including de novo drug design [<xref ref-type="bibr" rid="ref53">53</xref>].</p>
      <p>Drug repurposing comprises identifying existing drugs that could effectively act on proteins targeted by the virus. Recently, 332 high-confidence SARS-CoV-2 protein–human protein interactions have been experimentally identified, as well as 69 ligands, comprising drugs approved by the US Food and Drug Administration (FDA) and compounds in preclinical and clinical trials, which specifically target these interactions [<xref ref-type="bibr" rid="ref54">54</xref>]. Understanding which proteins and pathways in the host the virus targets during infection is crucial for the development of AI systems for drug repurposing.</p>
      <p>For instance, algorithms modeling the interaction between drugs and proteins have helped identify baricitinib, which was previously used for the treatment of arthritis, as a useful drug against COVID-19 [<xref ref-type="bibr" rid="ref55">55</xref>]. This drug inhibits the proteins that help the virus penetrate the host cell. Thanks to approaches that exploit the computational identification of relations between existing drugs and target molecules, research published by a team of Korean and American scientists has allowed the identification of FDA-approved antivirals that could potentially target the key proteins for COVID-19 [<xref ref-type="bibr" rid="ref56">56</xref>].</p>
      <p>The molecular processes of virus-host interactions have been recently reconstructed in an international effort coordinated by domain experts, called the COVID-19 Disease Map project [<xref ref-type="bibr" rid="ref57">57</xref>]. The project aims to maintain an open-access resource for continuous, curated integration of data and knowledge bases to support computational analysis and disease modeling. It represents a milestone of paramount importance for the development of AI systems for SARS-CoV-2 and their comparison with models of other coronaviruses. Moreover, by providing information about the intermolecular wiring of virus-host interactions, the project enables network-based AI modeling for COVID-19 drug repurposing, which has recently shown promising results by using network diffusion and network proximity [<xref ref-type="bibr" rid="ref58">58</xref>]. Moreover, deep neural networks largely employed in NLP, such as the Transformer architecture, have also been proposed for COVID-19 drug repurposing [<xref ref-type="bibr" rid="ref56">56</xref>].</p>
      <p>In the field of drug development, that is, the pharmacotherapeutic course of a newly identified lead compound, computational models have been proven extremely successful in facilitating a quicker, cheaper, and more effective development of new drugs [<xref ref-type="bibr" rid="ref59">59</xref>]. For instance, AI can map multidimensional characteristics of proteins to considerably speed up the research process in comparison to traditional methodologies such as x-ray crystallography. In this regard, AI is crucial in optimizing drug discovery pipelines and improving drug development outcomes, with estimated costs of US $2.6 billion [<xref ref-type="bibr" rid="ref59">59</xref>].</p>
      <p>Structural modeling and chemoinformatics methods for COVID-19 (eg, docking-based binding conformation studies of small molecules to target human or viral proteins) can greatly benefit from AI solutions. For instance, AI-based approaches have been used to infer structural similarities among molecules, such as algorithms that can model the graphical structure of chemical compounds through graph convolutional networks or other approaches [<xref ref-type="bibr" rid="ref60">60</xref>]. AI systems can also leverage knowledge about protein sequences to infer the activity of similar ones. As previously mentioned, Google DeepMind has managed to predict the structure of five proteins targeted by SARS-CoV-2, namely SARS-CoV-2 membrane protein, Nsp2, Nsp4, Nsp6, and papain-like proteinase (C-terminal domain) [<xref ref-type="bibr" rid="ref4">4</xref>]. The deep learning approach uses amino acid features from similar sequences, based on multiple sequence alignment, to infer the distribution of structural distances to predict the protein structures [<xref ref-type="bibr" rid="ref61">61</xref>].</p>
      <p>Finally, AI can also be used to synthetically generate new molecules, such as new chemical compounds. For instance, the biotech company Insilico Medicine used reinforcement learning to model small molecules and identify those that inhibit specific infection pathways. The team created a generative chemistry pipeline to design novel SARS-CoV-2 inhibitors to later be synthesized and tested. The pipeline employs a large array of generative models, including autoencoders, generative adversarial networks, and genetic algorithms optimized with reinforcement learning [<xref ref-type="bibr" rid="ref53">53</xref>].</p>
    </sec>
    <sec>
      <title>Pharmacogenomics and Vaccines</title>
      <p>Pharmacogenomics, which is the study of the role of genomic characteristics of an individual in drug response, represents a key gateway to personalized medicine [<xref ref-type="bibr" rid="ref62">62</xref>-<xref ref-type="bibr" rid="ref64">64</xref>]. Although the translation of genomic information into clinical practice is recognized as one of the most challenging aspects of the future of medicine [<xref ref-type="bibr" rid="ref65">65</xref>], the information about the genetic makeup of individual patients has the potential to guide clinical decision support and to facilitate biomedical research in many different areas. For instance, genomics can inform drug discovery by providing simultaneous insights into the disease mechanisms and potential targets for treating individual patients [<xref ref-type="bibr" rid="ref66">66</xref>].</p>
      <p>Pharmacogenomics approaches to COVID-19 are still in their infancy. Indeed, although the SARS-CoV-2 genome was published in draft on January 10, 2020 [<xref ref-type="bibr" rid="ref67">67</xref>], and real-time tracking of the pathogen evolution is now available [<xref ref-type="bibr" rid="ref68">68</xref>], much less genomic information is currently available about the host. Several studies focus on genetic variations associated with susceptibility to infection and clinical manifestations, including human leukocyte antigen (HLA) variants in the UK Biobank population-based cohort [<xref ref-type="bibr" rid="ref69">69</xref>] and angiotensin-converting enzyme 2 (ACE2) variants in the Italian population [<xref ref-type="bibr" rid="ref70">70</xref>]. Retrospective and prospective studies focusing on COVID-19 disease susceptibility and severity have been collected by the COVID-19 Host Genetics Initiative [<xref ref-type="bibr" rid="ref17">17</xref>,<xref ref-type="bibr" rid="ref18">18</xref>].</p>
      <p>Despite the absence of direct evidence of pharmacogenomics data in COVID-19 patients, the related literature for COVID-19 therapies, including hydroxychloroquine, ribavirin, and baricitinib, has been recently surveyed [<xref ref-type="bibr" rid="ref71">71</xref>]. Potential actionable genetic markers have been reported, namely, several genetic variants that can alter the pharmacokinetics of drugs that may affect the response to COVID-19 treatments. Importantly, as age, race, gender, and comorbidities have been associated with COVID-19 risk [<xref ref-type="bibr" rid="ref72">72</xref>], these factors are deemed warranted to assess their role in the variation of treatment responses and need further investigation.</p>
      <p>Population genetics is also needed to better understand the association between genetic variability and COVID-19. The importance and complexity of population genetic information, such as genome-wide association studies (GWAS), for drug discovery are exemplified by a study showing that 8% of drugs approved by the FDA target molecules with genetic support, whereas only 2% of phase-1 drugs are genetically supported [<xref ref-type="bibr" rid="ref73">73</xref>]. Despite such low rates, GWAS can help identify therapeutics that can be repurposed to treat individuals affected by diseases that are mechanistically related to those for which the drugs were developed [<xref ref-type="bibr" rid="ref74">74</xref>]. Insights from GWAS can also inform about better patient management and therapy, such as the case of variants in six genes on chromosome 3, namely <italic>SLC6A20</italic>, <italic>LZTFL1</italic>, <italic>CCR9</italic>, <italic>FYCO1</italic>, <italic>CXCR6</italic>, and <italic>XCR1</italic>, which have been recently associated with severe COVID-19 cases with respiratory failure [<xref ref-type="bibr" rid="ref75">75</xref>].</p>
      <p>Understanding population genetic heterogeneity is crucial for vaccine design, in particular, as it concerns the individual variability of the major histocompatibility complex (MHC-I and MHC-II) proteins, encoded by the <italic>HLA</italic> gene, which present SARS-CoV-2 epitopes to the immune system. Such individual variability, coupled with the importance of cellular immunity in the severity of the response to the infection, makes the identification of actionable targets for COVID-19 vaccines a challenging endeavor. AI models for COVID-19 vaccine development focus on the prediction of potential epitopes by using a variety of techniques, such as deep docking [<xref ref-type="bibr" rid="ref76">76</xref>], long short-term memory networks [<xref ref-type="bibr" rid="ref77">77</xref>], extreme gradient boosting [<xref ref-type="bibr" rid="ref78">78</xref>], as well as approaches that account for different <italic>HLA</italic> alleles by combining several existing machine learning tools [<xref ref-type="bibr" rid="ref79">79</xref>]. A recent survey of AI-based approaches to COVID-19 vaccine design [<xref ref-type="bibr" rid="ref80">80</xref>] suggests that the most popular candidate is the SARS-CoV-2 spike protein, which initiates the interaction with the host through the attachment to the ACE2 receptor [<xref ref-type="bibr" rid="ref81">81</xref>].</p>
    </sec>
    <sec>
      <title>Mining of the Medical Literature</title>
      <p>The staggering rate of publications about COVID-19, both in the form of preprints and peer-reviewed articles, is posing unprecedented challenges to knowledge acquisition and the information quality assessment process. A large part of content is produced by humans for humans, in the form of free text, where crucial pieces of information end up being buried. Because free text is not intelligible by machines, human intervention must identify the relevant pieces of information from the publications and turn it into a tabular form. Recent developments in NLP techniques have helped the automation of this process through machine learning and, in particular, deep learning algorithms [<xref ref-type="bibr" rid="ref82">82</xref>,<xref ref-type="bibr" rid="ref83">83</xref>]. Symptoms, patient demographics, clinical data, algorithms, performance, and limitations are identifiable in the texts by properly trained models, which can obtain comparable accuracy to humans at a much faster rate, making it finally possible to monitor the enormous volume of the literature produced [<xref ref-type="bibr" rid="ref84">84</xref>]. The resulting structured data can be exploited to enrich knowledge graphs (KGs) [<xref ref-type="bibr" rid="ref85">85</xref>-<xref ref-type="bibr" rid="ref87">87</xref>], which provide a means to represent and formalize information [<xref ref-type="bibr" rid="ref85">85</xref>,<xref ref-type="bibr" rid="ref88">88</xref>], analytical, relational, and inferential investigations and fill the knowledge gaps in the community. Moreover, to rationalize the immense quantity of information on COVID-19, new algorithms can generate low-dimensional representations of the KGs, allowing researchers for clustering and classification [<xref ref-type="bibr" rid="ref85">85</xref>,<xref ref-type="bibr" rid="ref89">89</xref>]. We list here representative KG efforts that have been directed at the fight against COVID-19 (see <xref ref-type="boxed-text" rid="box1">Textbox 1</xref>).</p>
      <boxed-text id="box1" position="float">
        <title>Knowledge graph resources for COVID-19.</title>
        <p>
          <bold>Project names and references:</bold>
        </p>
        <list list-type="bullet">
          <list-item>
            <p>KG-Covid-19 Knowledge Graph Hub [<xref ref-type="bibr" rid="ref90">90</xref>]</p>
          </list-item>
          <list-item>
            <p>COVID-19 Community Project [<xref ref-type="bibr" rid="ref91">91</xref>]</p>
          </list-item>
          <list-item>
            <p>COVID-KG [<xref ref-type="bibr" rid="ref92">92</xref>]</p>
          </list-item>
          <list-item>
            <p>CovidGraph [<xref ref-type="bibr" rid="ref93">93</xref>]</p>
          </list-item>
          <list-item>
            <p>COVID-19 Miner [<xref ref-type="bibr" rid="ref94">94</xref>]</p>
          </list-item>
          <list-item>
            <p>COVID-19 Biomedical Knowledge Miner [<xref ref-type="bibr" rid="ref95">95</xref>]</p>
          </list-item>
          <list-item>
            <p>COVID-19 Taxila [<xref ref-type="bibr" rid="ref96">96</xref>]</p>
          </list-item>
        </list>
      </boxed-text>
      <p>The KG-Covid-19 Knowledge Graph Hub project is the first Knowledge Graph Hub (KG-Hub) [<xref ref-type="bibr" rid="ref90">90</xref>] dedicated to COVID-19. KG-Hub is a software to download and transform data to a central location for building KGs from different combinations of data sources. The Covid-19 KG-Hub downloads and transforms data from more than 50 different COVID-19 databases of drugs, genes, proteins, ontologies, diseases, phenotypes, and publications and generates a KG that can be used for machine learning.</p>
      <p>The COVID-19 Community Project [<xref ref-type="bibr" rid="ref91">91</xref>] is a community-based KG that links heterogeneous datasets about COVID-19, in three main areas: the host, the virus, and the cellular environment. These KGs use several publicly available datasets, such as the CORD-19 dataset, a set of over 51,000 scholarly articles about coronaviruses [<xref ref-type="bibr" rid="ref97">97</xref>].</p>
      <p>Other notable databases used in KGs are the COVID-19 Data Portal (see Introduction) and The COVID-19 Drug and Gene Set Library [<xref ref-type="bibr" rid="ref98">98</xref>]. One of the tools that use these is the COVID-KG [<xref ref-type="bibr" rid="ref92">92</xref>], which embeds entities in the KG, such as papers, authors, or journals [<xref ref-type="bibr" rid="ref99">99</xref>].</p>
      <p>CovidGraph [<xref ref-type="bibr" rid="ref93">93</xref>] is a collaboration of researchers to build a research and communication platform that encompasses over 40,000 publications, case statistics, genes and functions, molecular data, and much more. The output is a KG in which entity relationships can be found and new pieces of literature can be discovered. Another tool that uses the CORD-19 dataset is COVID-19 Miner [<xref ref-type="bibr" rid="ref94">94</xref>], which provides access to a database of interactions among genes or proteins, chemicals, and biological processes related to SARS-CoV-2, which are automatically extracted using NLP from the CORD-19 dataset and manuscripts updated daily from the preprint servers medRxiv and bioRxiv [<xref ref-type="bibr" rid="ref100">100</xref>].</p>
      <p>Furthermore, COVID-19 Biomedical Knowledge Miner [<xref ref-type="bibr" rid="ref85">85</xref>,<xref ref-type="bibr" rid="ref95">95</xref>] is an intent to lay the foundation for a comprehensive and interactive KG in the context of COVID-19 that connects the causes and effects and enables users to completely explore the information contained therein. Data are supplied from papers available in PubMed and preprints available from platforms such as bioRxiv, chemRxiv, medRxiv, PrePrints, and Research Square. Lastly, COVID-19 Taxila [<xref ref-type="bibr" rid="ref96">96</xref>] is an AI and NLP system that uses thousands of COVID-19–related publications, clinical trials, and other relevant sources to enable users to search and analyze the COVID-19 literature. Publications and data are automatically updated.</p>
    </sec>
    <sec sec-type="discussion">
      <title>Discussion</title>
      <p>The COVID-19 pandemic has caused some of the most significant challenges that national health care systems have had to face in recent human history. These systems include not only hospitals but also a multitude of clinicians, retirement and nursing homes, families, and communities. Government lockdown policies undertaken to reduce hospital strain has impacted the society as a whole and has also had social and economic consequences, which have been more severe for minorities and vulnerable groups [<xref ref-type="bibr" rid="ref101">101</xref>]. Moreover, this pandemic is taking place in the age of social media and Web 2.0, which contain plenty of misinformation and fake news, and with no way for the average internet user to check the reliability of the sources. Nevertheless, the COVID-19 crisis has also shown the promise of technology in facilitating a better understanding of a complex disease and its impact on public health.</p>
      <p>Here, we illustrated examples of how AI can advance research and clinical medicine and prepare governments for future similar crises. AI shows promise to deliver models for outbreak analytics and detection, prevention, early intervention, and decision-making. We highlighted the unparalleled opportunity for AI to fill the gap between translational research and clinical medicine. Finally, in addition to the medical applications of AI, it is worth mentioning the potential of NLP for monitoring the quality of the information available to the public and fighting fake news [<xref ref-type="bibr" rid="ref102">102</xref>-<xref ref-type="bibr" rid="ref104">104</xref>].</p>
      <p>Thanks to the availability of big data and high-performance computing, the fight against the novel coronavirus can leverage the support of AI, as demonstrated by initiatives such as the COVID-19 High Performance Computing Consortium [<xref ref-type="bibr" rid="ref105">105</xref>]. This technology allows us to address, at a much higher speed and a comparable performance, complex tasks that cannot be executed by humans—who can now focus on more intelligence-demanding activities such as emotional intelligence and human-to-human bonding [<xref ref-type="bibr" rid="ref106">106</xref>].</p>
      <p>Although AI is traditionally trained on large datasets for identifying population-level patterns (ie, common characteristics among people belonging to some clinical classes), recent efforts have promoted the utilization of this technology in conjunction with the principles of precision medicine, to substitute the “average patient” [<xref ref-type="bibr" rid="ref42">42</xref>] with a real individual, based on geographical and socioeconomic signature as well as genetic, epigenetic, and other molecular profiles [<xref ref-type="bibr" rid="ref107">107</xref>]. Under this paradigm, AI is meant to empower clinicians to tailor interventions [<xref ref-type="bibr" rid="ref108">108</xref>] (whether preventive or therapeutic) to the nuanced—and often unique—features of every human being [<xref ref-type="bibr" rid="ref109">109</xref>]. To this end, multidimensional datasets, such as the variety of data modalities that are currently collected and modeled for COVID-19 [<xref ref-type="bibr" rid="ref110">110</xref>-<xref ref-type="bibr" rid="ref112">112</xref>], capture individual genetic, biochemical, physiological, environmental, and behavioral variations [<xref ref-type="bibr" rid="ref113">113</xref>] that may interfere with the development, progression, and treatment of a disease. Thanks to the drop in price of sequencing the human genome (from billions to hundreds of dollars in 30 years [<xref ref-type="bibr" rid="ref114">114</xref>]), it is now possible to exploit AI to study phenotypic, genotypic, and environmental correlations among diseases [<xref ref-type="bibr" rid="ref115">115</xref>]. With this approach, AI can predict the risk of an individual to develop a disease and estimate the likelihood of success for a treatment. In the case of COVID-19, this could lead to a better allocation of resources and an improved match between treatments and patients, consequently improving outcomes for preventive and therapeutic interventions. Therefore, AI-aided precision medicine connects some of the key benefits for a sustainable and effective health care system: efficiency, efficacy, and safety assessment [<xref ref-type="bibr" rid="ref30">30</xref>].</p>
      <p>AI is recognized as a necessity to achieve precision medicine in COVID-19. The current crisis has highlighted that a huge amount of work is still needed to exploit AI-based solutions to their full potential in order to transform health care. AI implementation in the clinical setting is still far from completion [<xref ref-type="bibr" rid="ref115">115</xref>]. The highly fragmented and diverse health care systems, absence of a protocol for documenting patient data, ethical constraints (such as privacy), and limitations of AI itself (eg, bias and non-interpretability) still represent serious challenges to extensive AI adoption [<xref ref-type="bibr" rid="ref116">116</xref>].</p>
    </sec>
  </body>
  <back>
    <app-group/>
    <glossary>
      <title>Abbreviations</title>
      <def-list>
        <def-item>
          <term id="abb1">ACE2</term>
          <def>
            <p>angiotensin-converting enzyme 2 </p>
          </def>
        </def-item>
        <def-item>
          <term id="abb2">AI</term>
          <def>
            <p>artificial intelligence</p>
          </def>
        </def-item>
        <def-item>
          <term id="abb3">AUROC</term>
          <def>
            <p>area under the receiver operating characteristic curve</p>
          </def>
        </def-item>
        <def-item>
          <term id="abb4">CNN</term>
          <def>
            <p>convolutional neural network</p>
          </def>
        </def-item>
        <def-item>
          <term id="abb5">CONSORT-AI</term>
          <def>
            <p>Consolidated Standards of Reporting Trials–Artificial Intelligence</p>
          </def>
        </def-item>
        <def-item>
          <term id="abb6">CT</term>
          <def>
            <p>computed tomography</p>
          </def>
        </def-item>
        <def-item>
          <term id="abb7">FDA</term>
          <def>
            <p>Food and Drug Administration</p>
          </def>
        </def-item>
        <def-item>
          <term id="abb8">GWAS</term>
          <def>
            <p>genome-wide association studies</p>
          </def>
        </def-item>
        <def-item>
          <term id="abb9">HLA</term>
          <def>
            <p>human leukocyte antigen</p>
          </def>
        </def-item>
        <def-item>
          <term id="abb10">ICU</term>
          <def>
            <p>intensive care unit</p>
          </def>
        </def-item>
        <def-item>
          <term id="abb11">KG</term>
          <def>
            <p>knowledge graph</p>
          </def>
        </def-item>
        <def-item>
          <term id="abb13">LASSO</term>
          <def>
            <p>least absolute shrinkage and selection operator</p>
          </def>
        </def-item>
        <def-item>
          <term id="abb14">NLP</term>
          <def>
            <p>natural language processing</p>
          </def>
        </def-item>
        <def-item>
          <term id="abb15">SPIRIT-AI</term>
          <def>
            <p>Standard Protocol Items: Recommendations for Interventional Trials–Artificial Intelligence</p>
          </def>
        </def-item>
      </def-list>
    </glossary>
    <ack>
      <p>We are deeply thankful to the Women’s Brain Project (WBP) (www.womensbrainproject.com), an international organization advocating for women’s brain and mental health through scientific research, debate, and public engagement. The authors would like to thank Maria Teresa Ferretti and Shahnaz Radjy for the helpful comments. DC, AM, and AV have received funding from the European Commission’s Horizon 2020 Program H2020-SC1-DTH-2018-1, “iPC-individualizedPaediatricCure” (ref. 826121), and H2020-ICT-2018-2, “INFORE-Interactive Extreme-Scale Analytics and Forecasting” (ref. 825070).</p>
    </ack>
    <fn-group>
      <fn fn-type="con">
        <p>ES and NM conceived the study with the contribution of ASC, EC, and DC. ES and NM directed the content selection and design, assisted by EC, DC, and AM. AV, KH, and CL supervised the project. The corresponding author had the final responsibility for the decision to submit the manuscript for publication. All authors have contributed to the writing and editing of the manuscript and have read and approved the final manuscript.</p>
      </fn>
      <fn fn-type="conflict">
        <p>ASC and ES are currently employees at Biogen International GmbH, HQ, Switzerland, and Bayer Pharmaceuticals, USA, respectively. The other authors declare no competing interests. KH is a founder and owns equity of CRA Health (formerly Hughes RiskApps), is co-creator of Ask2Me.Org, which is licensed for commercial use by the Dana-Farber Cancer Institute, and receives honoraria from Myriad Genetics.</p>
      </fn>
    </fn-group>
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