Pregnancy outcomes in women with primary Sjögren's syndrome: an analysis of data from the multicentre, prospective, GR2 study

医学 妊娠期 产科 人口 怀孕 前瞻性队列研究 妇科 儿科 内科学 遗传学 生物 环境卫生
作者
Grégoire Martin de Frémont,N. Costedoat‐Chalumeau,Estibaliz Lazaro,Rakiba Belkhir,G. Guettrot-Imbert,Nathalie Morel,Gaëtane Nocturne,Anna Moltó,Tiphaine Goulenok,Élisabeth Diot,Laurent Pérard,Nicole Ferreira-Maldent,M. Le Besnerais,Nicolas Limal,Nihal Martis,Noémie Abisror,O. Debouverie,Christophe Richez,Vincent Sobanski,F. Maurier,Gaétan Sauvètre,H. Lévesque,Marie-Agnès Timsit,N. Tieulié,P. Orquevaux,Boris Bienvenu,Matthieu Mahévas,Thomas Papo,Céline Lartigau-Roussin,E. Chauvet,E. Berthoux,F. Sarrot-Reynauld,L. Raffray,Marion Couderc,Nicolas Martin Silva,Noémie Jourde‐Chiche,Nicolas Belhomme,Thierry Thomas,Vincent Poindron,Viviane Queyrel-Moranne,Juliette Delforge,Camille Le Ray,E. Pannier,Xavier Mariette,Véronique Le Guern,Raphaèle Séror,Alexandra Audemard‐Verger,Emmanuel Azzi,Béatrice Banneville,Antoine Baudet,C. Bazire,C. Bélizna,Alexandre Bélot,Y. Benhamou,A. Bérezné,Fanny Bernard-Guervilly,S. Berthier,H. Bézanahary,Lisa Bialé,A. Bigot,D. Launay,Anne Calas,J. Campagne,P. Cathébras,C. Cazalets,Benjamin Chaigne,Olivia Chandesris,Jérémy Chatelais,Emmanuel Chatelus,Fleur Cohen,Bernard Combe,Céline Comparon,Pascal Coquerelle,Louise Damian,Éric Daugas,Mathilde de Menthon,Claire de Moreuil,Estelle Delattre,Azeddine Dellal,Catherine Deneux‐Tharaux,Amélie Denis,Camille Deprouw,Emmanuelle Dernis,A. Deroux,Sandra Desouches,Philippe Dieudé,Guillaume Direz,Maxime Dougados,Marine Driessen,A. Du‐Thanh,L. Dunogeant,C. Durant,Cécile‐Audrey Durel,I. Durieu,Florence Eboué,Elisabeth Éléfant,Olivier Fain,Bruno Fautrel,René‐Marc Flipo,Aline Frazier,Antoine Froissart,Sophie Georgin‐Lavialle,Elisabeth Gervais,Bertrand Godeau,François Goffinet,Anne Gompel,Laure Gossec,Philippe Goupille,C. Grangé,Constance Guillaud-Danis,É. Hachulla,S. Hoefsloot,Aurélie Hummel,P. Jégo,Stéphanie Jobard,L. Josselin-Mahr,M. Lambert,Vincent Langlois,Delphine Larivière,C. Larroche,Augustin Latourte,Christian Lavigne,Thomas Le Gallou,Gaëlle Leroux,Jean Guillaume LETAROUILLY,Frédéric Lioté,Laurence Lœuillet,Jonathan London,Valentine Loustau,P. Lozac’h,E. Maheu,Hélène Maillard,Hubert Marotte,A. Masseau,A. Mékinian,Sara Melboucy Belkhir,Corinne Miceli-Richard,Martin Michaud,Marc Michel,Olivier Moranne,Chafika Morati-Hafsaoui,Guillaume Moulis,Luc Mouthon,Barbara NICOLAS,J. Nizard,Jérémy Ora,R. Outh,Élisabeth Pasquier,Jean‐Loup Pennaforte,Antoinette Perlat,Hélène PETIT-BAUER,Évangéline Pillebout,Jean-Maxime Piot,Agnès Portier,O. Pourrât,Xavier Puéchal,G. Pugnet,Manon Redondin,Alexis Régent,Mélanie Roriz,L. Sailler,Léa Savey,Marc Scherlinger,N. Schleinitz,Jérémie Sellam,Loı̈c Sentilhes,Aude Servais,P. Smets,Christelle Sordet,Martin Soubrier,Katia Stankovic‐Stojanovic,G. Urbanski,V. Veit,Emmanuelle Weber,Cécile Yelnik
出处
期刊:The Lancet Rheumatology [Elsevier]
卷期号:5 (6): e330-e340 被引量:11
标识
DOI:10.1016/s2665-9913(23)00099-1
摘要

Background Adverse pregnancy outcomes in women with primary Sjögren's syndrome have only been evaluated retrospectively using heterogeneous methods and with contradictory results. We aimed to describe adverse pregnancy, delivery, and birth outcome risks in pregnant women with primary Sjögren's syndrome compared with those of a matched general population in France, and to identify factors predictive of disease flares or adverse pregnancy outcomes. Methods We conducted a multicentre, prospective, cohort study in France using the GR2 (Groupe de Recherche sur la Grossesse et les Maladies Rares) registry. Women from the GR2 study were eligible if they had conceived before March, 2021, had primary Sjögren's syndrome according to the American College of Rheumatology and European Alliance of Associations for Rheumatology (EULAR) 2016 classification criteria, and had an ongoing pregnancy at 12 weeks of gestation. In women who entered in the registry with pregnancies before 18 weeks of gestation, we sought to identify factors associated with primary Sjögren's syndrome flare (≥3-point increase in EULAR Sjögren's Syndrome Disease Activity Index [ESSDAI] score) or adverse pregnancy outcomes (fetal or neonatal death, placental insufficiency leading to a preterm delivery [<37 weeks of gestation], or small-for-gestational-age birthweight). A matched controlled study compared adverse pregnancy, delivery, and birth outcome rates between pregnant women with primary Sjögren's syndrome from the GR2 registry and matched controls from the general population included in the last French perinatal survey (Enquête Nationale Périnatale 2016). Findings 1944 pregnancies were identified in the GR2 cohort, of which 106 pregnancies in 96 women with primary Sjögren's syndrome were included in this analysis. The median age at pregnancy onset was 33 years (IQR 31–36). 87 (83%) of 105 pregnancies (with ethnicity data) were in White women, 18 (17%) were in Black women; 92 (90%) of 102 had previous systemic activity (ESSDAI score of ≥1; data missing in four pregnancies), and 48 (45%) of 106 had systemic activity at inclusion. Of 93 pregnancies included at week 18 of gestation or earlier, primary Sjögren's syndrome flares occurred in 12 (13%). No baseline parameters were associated with primary Sjögren's syndrome flare. Four twin pregnancies and one medical termination were excluded from the adverse pregnancy outcome analysis; of the remaining 88, adverse pregnancy outcomes occurred in six (7%). Among pregnancies in women with data for antiphospholipid antibodies (n=55), antiphospholipid antibody positivity was more frequent among pregnancies with adverse outcomes (two [50%] of four pregnancies) compared with those without adverse outcomes (two [4%] of 51 pregnancies; p=0·023). Anti-RNP antibody positivity was also more frequent among pregnancies with adverse outcomes than those without, although this was not statistically significant. In the matched controlled study, adverse pregnancy outcomes occurred in nine (9%) of 105 pregnancies in women with primary Sjögren's syndrome and 28 (7%) of the 420 matched control pregnancies; adverse pregnancy outcomes were not significantly associated with primary Sjögren's syndrome (odds ratio 1·31, 95% CI 0·53–2·98; p=0·52). Interpretation Pregnancies in women with primary Sjögren's syndrome had very good prognoses for mothers and fetuses, with no overall increase in adverse pregnancy outcome risk compared with the general population. Women with antiphospholipid antibodies or anti-RNP antibodies require close monitoring, because these factors might be associated with a higher risk of adverse pregnancy outcomes. Funding Lupus France, Association des Sclérodermiques de France, Association Gougerot Sjögren, Association Francophone Contre la Polychondrite Chronique Atrophiante, AFM-Telethon, Société Nationale Française de Médecine Interne, Société Française de Rhumatologie, Cochin Hospital, French Health Ministry, Fondation for Research in Rheumatology, Association Prix Véronique Roualet, Union Chimique Belge.
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