Molecular imaging—The first visual themed issue published in the <i>British Journal of Pharmacology</i>
Notice bibliographique
Résumé
This article is part of a themed issue on Molecular imaging - visual themed issue. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v178.21/issuetoc With this British Journal of Pharmacology ‘Molecular imaging - visual themed issue’, we have provided an up-to-date account of a select group of molecular imaging techniques that we believe have and will enable interrogation of the pharmacology of novel compounds and ultimately to the development of new therapeutic agents. Molecular imaging is the visualization and quantification of molecules within living patients. Revealing information on biomarkers and cellular and molecular pathways can improve disease diagnosis and therapeutic intervention. In addition, these advanced techniques also offer opportunities to identify novel pharmacological targets, thus facilitating both drug discovery and treatment stratification. The optimum molecular imaging modality ideally should possess high sensitivity and resolution, an acceptable safety profile, and be capable of non-invasive quantitative multiplex imaging. Currently, there are no clinical imaging modalities routinely used in the clinic for molecular imaging; therefore, new approaches are required to meet this goal. The focus of this British Journal of Pharmacology visual-themed issue is on cardiovascular medicine and cancer. This themed issue is not meant to provide an exhaustive list of molecular imaging modalities for our topic areas, rather it is deliberately focused on a few select approaches to test a completely new ‘visual’ layout for the British Journal of Pharmacology. Each of the four invited reviews has been designed and presented in a format with a predominance of visual material over text. Seeing is believing as they say, and so we have attempted to select the most helpful representative images and videos for each topic covered, to guide the readers through the respective merits and limitations of established and emerging imaging modalities, whilst also highlighting their potential theranostics applications. Video podcasts and figures, available in PowerPoint format, complement each published article. The themed issue starts with an article by MacRitchie et al. (2021). The authors provide an overview of molecular imaging of cardiovascular inflammation. Immuno-inflammatory responses play key roles in the development and clinical manifestation of several cardiovascular diseases (CVD) (Libby et al., 2018; Rodriguez-Iturbe et al., 2017; Schloss et al., 2020). However, routinely used medical imaging modalities are restricted to anatomical or functional imaging and are unable to reveal the cellular and molecular inflammatory pathways at the level of resolution required for a more timely and precise diagnosis and pharmacological treatment (MacRitchie et al., 2020). In this visual review, the authors discuss strengths and weaknesses of molecular imaging modalities in CVD, spanning from those already being used in the clinic such as magnetic resonance imaging (MRI) and positron emission tomography (PET), to novel technologies emerging at the pre-clinical stage. In CVD, not only does inflammation cause thrombosis but the opposite is also true, that thrombosis can trigger inflammation (Stark & Massberg, 2021). As such, faster and more reliable imaging modalities for the diagnosis of thrombosis are needed. In this visual issue, Wang et al. (2021) discuss the state-of-the-art in molecular imaging of arterial and venous thrombosis, highlighting recent improvements in the identification of biomarkers for thromboembolic diseases; the development of optimized contrast agents with improved signal to noise ratio and recent developments in scanner technologies with higher sensitivity and resolution. The review covers modalities used for the clinical imaging of thrombosis, including PET, MRI, X-ray computed tomography (CT), and ultrasound imaging, to preclinical fluorescence and bioluminescent imaging modalities. A clear demonstration of the potential to translate molecular imaging into clinical practice is presented in the review of Kotanidis and Antoniades (2021), providing a virtual guide to perivascular fat imaging using CT. The authors discuss their recent elegant work (Antonopoulos et al., 2017; Oikonomou et al., 2018; Oikonomou et al., 2019), demonstrating non-invasive phenotyping of perivascular adipose tissue (PVAT) using CT as a promising marker for early detection of vascular inflammation in atherosclerosis. In particular, they highlight the use of the Perivascular Fat Attenuation Index (FAIPVAT) for cardiovascular risk stratification and the diagnostic and prognostic value of macroscopic adipose tissue radiomics. Along similar lines, the use of artificial intelligence (AI), a set of advanced computational algorithms that can accurately perform predictions for decision support, is thoroughly covered in the fourth visual review article by Klein et al. (2021), where the authors discuss the use of AI for solid tumour diagnosis in digital pathology. With digital pathology, specimen slides are digitized and analysed using AI. AI-assisted analysis improves accuracy, speed and image analysis workflows. Developments in this field, enabling rapid and uniform analysis of large numbers of slides from any single tissue sample or patient, will inevitably lead to more informed pharmacotherapy decisions and improved prediction of therapy response outcomes and thus a better quality of care, coupled with reduced healthcare costs. In summary, this first visual-themed issue of the British Journal of Pharmacology provides readers with a pictorial representation of key emerging molecular imaging techniques and analysis approaches, mainly focusing on cardiovascular medicine and cancer. We plan to use this novel format to cover other topics in future issues of the Journal, allowing readers to ‘see’ results as they are reading them. We hope that the increased use of visual material across a variety of formats will help to convey complex information and highlight key messages. We thank all authors who contributed to this Research Topic. The group led by PM is funded by the British Heart Foundation (grants PG/19/84/34771, PG/21/10541); the Engineering and Physical Sciences Research Council (EPSRC) (grant EP/L014165/1); the Wellcome Trust (grant 204820/Z/16/Z); the University of Glasgow Scottish Funding Council and the Global Challenges Research Fund; the Erasmus+ International Credit Mobility (ICM) (grant 2020-1-UK01-KA107-078782); and FRA 2020 - Linea A, University of Naples Federico II/Compagnia di San Paolo. The authors wish to acknowledge that PM has co-authored papers with Karlheinz Peter, Charalambos Antoniades and Maria Chiara Maiuri. CA has co-authored papers with Karlheinz Peter and Pasquale Maffia. CA is a founder and shareholder of Caristo Diagnostics Ltd., a CT image analysis company. CA methods for analysis of the perivascular fat attenuation index described in this editorial are subject to patent PCT/GB2015/052359 and patent applications PCT/GB2017/053262, GB2018/1818049.7, GR20180100490, and GR20180100510, licensed through exclusive license to Caristo Diagnostics.
Récupéré en direct depuis OpenAlex et désinversé. Les résumés ne sont pas conservés dans cette base de données : les index inversés représentent 8,6 Go des 9,3 Go de texte de la base, et le serveur dispose de 13 Go libres.
Comment cette classification a été obtenuedéplier
Prédiction machine sur la base complète
Imitation des enseignantsNi prévalence calibrée, ni vérité terrain. Validation humaine à venir. Le volet Gemma est une étiquette directe du modèle pour chaque travail de la base, lue sur la notice réduite au titre. Le volet Codex est un classifieur appris des 10 348 étiquettes directes de Codex et calibré sur les taux pondérés de l'échantillon; les champs sans appui suffisant ne portent aucun appel Codex. Le mode candidate est l'union des deux volets; le consensus est leur intersection. Ces sorties portent le statut machine_predicted_unvalidated et ne sont pas des étiquettes humaines.
Scores du classifieur distillé par catégorie (deux têtes)
| Catégorie | Codex | Gemma |
|---|---|---|
| Métarecherche | 0,002 | 0,004 |
| Méta-épidémiologie (sens strict) | 0,001 | 0,001 |
| Méta-épidémiologie (sens large) | 0,001 | 0,001 |
| Bibliométrie | 0,003 | 0,001 |
| Études des sciences et des technologies | 0,001 | 0,001 |
| Communication savante | 0,007 | 0,003 |
| Science ouverte | 0,002 | 0,002 |
| Intégrité de la recherche | 0,004 | 0,004 |
| Charge utile insuffisante (le modèle a refusé de juger) | 0,337 | 0,150 |
Scores machine (provisoires)
Les deux têtes enseignantes du modèle étudiant, lues sur ce travail. Un score ordonne la base pour la relecture; il n'affirme jamais une catégorie, et le statut de validation accompagne chaque rangée tel quel.
Scores de référence d'un modèle non mature (critères de maturité non atteints, 7 itérations). Un score ordonne; il n'affirme jamais une catégorie.
score_only:v0-immature-baseline · tel quel depuis la passe de notation : score_only signifie que le nombre peut ordonner les travaux, et qu'aucune étiquette de catégorie n'en découleClassification
machine, non validéePrédiction automatique; un appel candidat d’une seule source (Gemma direct ou Codex distillé), pas un consensus.
Le détail, modèle par modèle et score par score, se trouve en fin de page sous « Comment cette classification a été obtenue ».