TY - JOUR
T1 - Incidences and risk factors of organ manifestations in the early course of systemic sclerosis
T2 - A longitudinal EUSTAR study
AU - EUSTAR co-authors
AU - Jaeger, Veronika K.
AU - Wirz, Elina G.
AU - Allanore, Yannick
AU - Rossbach, Philipp
AU - Riemekasten, Gabriela
AU - Hachulla, Eric
AU - Distler, Oliver
AU - Airò, Paolo
AU - Carreira, Patricia E.
AU - Gurman, Alexandra Balbir
AU - Tikly, Mohammed
AU - Vettori, Serena
AU - Damjanov, Nemanja
AU - Müller-Ladner, Ulf
AU - Distler, Jörg H.W.
AU - Li, Mangtao
AU - Walker, Ulrich A.
AU - Ananieva, Lidia
AU - Heitmann, Stefan
AU - Rednic, Simona
AU - Riccieri, Valeria
AU - Szmyrka-Kaczmarek, Magdalena
AU - Farge, Dominique
AU - Lapadula, Giovanni
AU - Matucci-Cerinic, Marco
AU - Guiducci, Serena
AU - Hunzelmann, Nicolas
AU - Ricci, Massimo
AU - Mihai, Carina
AU - Veale, Douglas
AU - Hesselstrand, Roger
AU - Mariok, Eduardo
AU - Smith, Vanessa
AU - Tarner, Ingo H.
AU - Kucharz, Eugene J.
AU - Czirják, László
AU - Martinovic, Duska
AU - Solanki, Kamal
AU - Ancuta, Codrina Mihaela
AU - Sibilia, Jean
AU - Paola, Caramaschi
AU - Hassanien, Manal
AU - Kahl, Sarah
AU - Wigley, Frederick
AU - Vanthuyne, Marie
AU - Opris, Daniela
AU - Radominski, Sebastião C.
AU - Monaco, Andrea Lo
AU - Corrado, Ada
AU - Litinsky, Ira
N1 - Publisher Copyright:
© 2016 Jaeger et al.This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2016/10
Y1 - 2016/10
N2 - Objective Systemic sclerosis (SSc) is a rare and clinically heterogeneous autoimmune disorder characterised by fibrosis and microvascular obliteration of the skin and internal organs. Organ involvement mostly manifests after a variable period of the onset of Raynaud's phenomenon (RP). We aimed to map the incidence and predictors of pulmonary, cardiac, gastrointestinal (GI) and renal involvement in the early course of SSc. Methods In the EUSTAR cohort, patients with early SSc were identified as those who had a visit within the first year after RP onset. Incident SSc organ manifestations and their risk factors were assessed using Kaplan-Meier methods and Cox regression analysis. Results Of the 695 SSc patients who had a baseline visit within 1 year after RP onset, the incident non-RP manifestations (in order of frequency) were: skin sclerosis (75%) GI symptoms (71%), impaired diffusing capacity for monoxide<80% predicted (65%), DU (34%), cardiac involvement (32%), FVC<80% predicted (31%), increased PAPsys>40mmHg (14%), and renal crisis (3%). In the heart, incidence rates were highest for diastolic dysfunction, followed by conduction blocks and pericardial effusion. While the main baseline risk factor for a short timespan to develop FVC impairment was diffuse skin involvement, for PAPsys>40mmHg it was higher patient age. The main risk factors for incident cardiac manifestations were antitopoisomerase autoantibody positivity and older age. Male sex, anti-RNA-polymerase-III positivity, and older age were risk factors associated with incident renal crisis. Conclusion In SSc patients presenting early after RP onset, approximately half of all incident organ manifestations occur within 2 years and have a simultaneous rather than a sequential onset. These findings have implications for the design of new diagnostic and therapeutic strategies aimed to 'widen' the still very narrow 'window of opportunity'. They may also enable physicians to counsel and manage patients presenting early in the course of SSc more accurately.
AB - Objective Systemic sclerosis (SSc) is a rare and clinically heterogeneous autoimmune disorder characterised by fibrosis and microvascular obliteration of the skin and internal organs. Organ involvement mostly manifests after a variable period of the onset of Raynaud's phenomenon (RP). We aimed to map the incidence and predictors of pulmonary, cardiac, gastrointestinal (GI) and renal involvement in the early course of SSc. Methods In the EUSTAR cohort, patients with early SSc were identified as those who had a visit within the first year after RP onset. Incident SSc organ manifestations and their risk factors were assessed using Kaplan-Meier methods and Cox regression analysis. Results Of the 695 SSc patients who had a baseline visit within 1 year after RP onset, the incident non-RP manifestations (in order of frequency) were: skin sclerosis (75%) GI symptoms (71%), impaired diffusing capacity for monoxide<80% predicted (65%), DU (34%), cardiac involvement (32%), FVC<80% predicted (31%), increased PAPsys>40mmHg (14%), and renal crisis (3%). In the heart, incidence rates were highest for diastolic dysfunction, followed by conduction blocks and pericardial effusion. While the main baseline risk factor for a short timespan to develop FVC impairment was diffuse skin involvement, for PAPsys>40mmHg it was higher patient age. The main risk factors for incident cardiac manifestations were antitopoisomerase autoantibody positivity and older age. Male sex, anti-RNA-polymerase-III positivity, and older age were risk factors associated with incident renal crisis. Conclusion In SSc patients presenting early after RP onset, approximately half of all incident organ manifestations occur within 2 years and have a simultaneous rather than a sequential onset. These findings have implications for the design of new diagnostic and therapeutic strategies aimed to 'widen' the still very narrow 'window of opportunity'. They may also enable physicians to counsel and manage patients presenting early in the course of SSc more accurately.
UR - http://www.scopus.com/inward/record.url?scp=84992018224&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0163894
DO - 10.1371/journal.pone.0163894
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C2 - 27706206
AN - SCOPUS:84992018224
SN - 1932-6203
VL - 11
JO - PLoS ONE
JF - PLoS ONE
IS - 10
M1 - e0163894
ER -