Italian National Registry of Alopecia Areata: An Epidemiological Study of 699 Italian Patients

    Bianca Maria Piraccini, Luca Rapparini, Federico Quadrelli, Aurora Alessandrini, Francesca Bruni, Stephano Cedirian, Francesca Pampaloni, Emanuela Marcelli, Barbara Bortolani, Enrico Giampieri, Giuseppe Gallo, Francesca Torrelli, Nadia Sciamarrelli, Pietro Quaglino, Carlo Tomasini, Stefania Barruscotti, Francesca Ambrogio, Caterina Foti, Michele Picciallo, Gemma Caro, Alfredo Rossi, Giovanni Pellacani, Lorenzo Ala, Maria Cristina Acri, Laura Diluvio, Enrico Matteini, Luca Bianchi, Giuseppe Argenziano, Graziella Babino, Elisabetta Fulgione, Laura Gnesotto, Andrea Sechi, Luigi Naldi, F. Tassone, Ketty Peris, Giacomo Caldarola, Raffaele Dante Caposiena, Giulia Bazzacco, Iris Zalaudek, Maria Giovanna Vastarella, Mariateresa Cantelli, Angela Patrì, Federica Dall’Oglio, Francesco Lacarrubba, Giuseppe Micali, Alessandro Fraghì, Valeria Boccaletti, Angelo Valerio Marzano, Mauro Barbareschi, Martina Silvio, Emanuele Vagnozzi, Maria Concetta Fargnoli, Chiara Caponio, Laura Atzori, Silvia Sanna, Jasmine Anedda, Claudio Feliciani, Maria Beatrice De Felici Del Giudice, Ilaria Scandagli, Francesca Prignano, Franco Rongioletti, Antonio Podo Brunetti, Gianmarco D Bigotto, Anna Maria Offidani, Oriana Simonetti, Serena Lembo, Annunziata Raimondo, Riccardo Balestri, Tommaso Ioris, Paolo Gisondi, Francesco Bellinato, Emanuele Trovato, Élisa Cinotti, Manuela Papini, Michela Cicoletti, Monica Corazza, Michela Starace
    TLDR Alopecia areata is hard to manage and affects quality of life.
    The study on the Italian National Registry of Alopecia Areata involved 699 Italian patients and aimed to evaluate the epidemiological data of those with alopecia areata (AA). The registry serves as a model for recording detailed information on the disease's course, associated conditions, and response to traditional treatments. The findings confirm that AA is a challenging condition to manage due to its unpredictable and often chronic-relapsing nature, significantly impacting patients' quality of life. The registry has proven to be an effective tool for standardizing data collection and monitoring new therapies.
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