Post-Acute Infectious Syndromes (PAIS) refer to the symptoms persisting months after initial infection. Clinical research studies on this topic often collect rich, multi-modal datasets. Yet, the complexity of the datasets and the lack of a precise clinical case definition pose difficulties in creating comprehensive analyses. Here, we present a generalisable framework for analysing data from longitudinal studies of PAIS using Latent Transition Analysis (LTA). It enables the identification of disease phenotypes and the patient-level analysis of transitions between them, without relying on predefined clinical categorisations. Furthermore, we introduce a method for incorporating covariate information, which enables exploration of how patient characteristics influence disease trajectories. We apply this methodology to the ORCHESTRA dataset, composed of individuals affected by SARS-CoV-2 infection from multiple European centres, for investigation into Post-COVID-19 condition (PCC). 5094 patient assessments were collected at SARS-CoV-2 infection, and at 6, 12, 18, and 24 months of follow-up. Our model identifies distinct PCC phenotypes with patient trajectories impacted by age and sex. Our results highlight how LTA can enhance the interpretability of complex, time-resolved clinical data, support personalized patient monitoring and management, and accelerate therapeutic development for other PAISs, too.

Latent transition analysis for longitudinal studies of post-acute infection syndromes

Canziani, Lorenzo Maria;Gentilotti, Elisa;Mazzaferri, Fulvia;Del Piccolo, Lidia;Tacconelli, Evelina
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Elena Addis;Maddalena Armellini;Anna Maria Azzini;Benedetta Barana;Elena Carrara;Alessandro Castelli;Filippo Cioli Puviani;Michela Conti;Carmine Cutone;Ruth Joanna Davis;Pasquale De Nardo;Daniele Fasan;Giada Fasani;Giorgia Franchina;Jacopo Garlasco;Enrico Gibbin;Salvatore Hermes Dall'O';Chiara Konishi De Toffoli;Lorenza Lambertenghi;Federico Lattanzi;Andrea Leonardi;Gaia Maccarrone;Massimo Mirandola;Matteo Morra;Alessandra Nazeri;Matilde Rocchi;Giulia Rosini;Chiara Perlini;Maria Diletta Pezzani;Laura Rovigo;Anna Giulia Salvadori;Alessia Savoldi;Rebecca Scardellato;Marcella Sibani;Lorenzo Tavernaro;Giorgia Tomassini;Alessandro Visentin;Stefania Vitali;Andrea Volpe;Chiara Zanchi;Gloria Mazzali;Giovanni Stabile;Gianluca Vantini;Riccardo Cecchetto;Davide Gibellini;Nicolò Cardobi;Maria Paola Cecchini;Anna Mason;Salvatore Monaco;Marco Pattaro Zonta;Cinzia Perlini;Gianluigi Zanusso;Elda Righi;Mariana Nunes Pinho Guedes;Maria Mongardi;Concetta Sciammarella;Claudio Micheletto;Paolo Gisondi;
2026-01-01

Abstract

Post-Acute Infectious Syndromes (PAIS) refer to the symptoms persisting months after initial infection. Clinical research studies on this topic often collect rich, multi-modal datasets. Yet, the complexity of the datasets and the lack of a precise clinical case definition pose difficulties in creating comprehensive analyses. Here, we present a generalisable framework for analysing data from longitudinal studies of PAIS using Latent Transition Analysis (LTA). It enables the identification of disease phenotypes and the patient-level analysis of transitions between them, without relying on predefined clinical categorisations. Furthermore, we introduce a method for incorporating covariate information, which enables exploration of how patient characteristics influence disease trajectories. We apply this methodology to the ORCHESTRA dataset, composed of individuals affected by SARS-CoV-2 infection from multiple European centres, for investigation into Post-COVID-19 condition (PCC). 5094 patient assessments were collected at SARS-CoV-2 infection, and at 6, 12, 18, and 24 months of follow-up. Our model identifies distinct PCC phenotypes with patient trajectories impacted by age and sex. Our results highlight how LTA can enhance the interpretability of complex, time-resolved clinical data, support personalized patient monitoring and management, and accelerate therapeutic development for other PAISs, too.
2026
COVID-19; data set; infectious disease; longitudinal gradient; research method
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11562/1182808
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