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Pregnancy outcomes in women with primary Sjögren's syndrome: an analysis of data from the multicentre, prospective, GR2 study.
de Frémont, Grégoire Martin; Costedoat-Chalumeau, Nathalie; Lazaro, Estibaliz; Belkhir, Rakiba; Guettrot-Imbert, Gaëlle; Morel, Nathalie; Nocturne, Gaétane; Molto, Anna; Goulenok, Tiphaine; Diot, Elisabeth; Perard, Laurent; Ferreira-Maldent, Nicole; Le Besnerais, Maelle; Limal, Nicolas; Martis, Nihal; Abisror, Noémie; Debouverie, Odile; Richez, Christophe; Sobanski, Vincent; Maurier, François; Sauvetre, Gaëtan; Levesque, Hervé; Timsit, Marie-Agnès; Tieulié, Nathalie; Orquevaux, Pauline; Bienvenu, Boris; Mahevas, Matthieu; Papo, Thomas; Lartigau-Roussin, Céline; Chauvet, Elodie; Berthoux, Emilie; Sarrot-Reynauld, Françoise; Raffray, Loïc; Couderc, Marion; Silva, Nicolas Martin; Jourde-Chiche, Noémie; Belhomme, Nicolas; Thomas, Thierry; Poindron, Vincent; Queyrel-Moranne, Viviane; Delforge, Juliette; Le Ray, Camille; Pannier, Emmanuelle; Mariette, Xavier; Le Guern, Véronique; Seror, Raphaèle.
Afiliação
  • de Frémont GM; APHP, Hôpital Bicêtre, Service de Rhumatologie, Centre de Référence Maladies Auto-Immunes et Systémiques Rares d'Île-de-France, Inserm UMR 1184, Center for Immunology of Viral Infections and Autoimmune Diseases, Université Paris-Saclay, Le Kremlin-Bicêtre, France.
  • Costedoat-Chalumeau N; APHP, Hôpital Cochin, Service de Médecine Interne, Centre de Référence Maladies Auto-Immunes et Systémiques Rares d'Île-de-France, Paris, France; Centre de Recherche Epidémiologie et Biostatistiques de Sorbonne Paris Cité, Université de Paris, Paris, France.
  • Lazaro E; CHU de Bordeaux, Service de Médecine Interne et Maladies Infectieuses, Bordeaux, France.
  • Belkhir R; APHP, Hôpital Bicêtre, Service de Rhumatologie, Centre de Référence Maladies Auto-Immunes et Systémiques Rares d'Île-de-France, Inserm UMR 1184, Center for Immunology of Viral Infections and Autoimmune Diseases, Université Paris-Saclay, Le Kremlin-Bicêtre, France.
  • Guettrot-Imbert G; APHP, Hôpital Cochin, Service de Médecine Interne, Centre de Référence Maladies Auto-Immunes et Systémiques Rares d'Île-de-France, Paris, France.
  • Morel N; APHP, Hôpital Cochin, Service de Médecine Interne, Centre de Référence Maladies Auto-Immunes et Systémiques Rares d'Île-de-France, Paris, France.
  • Nocturne G; APHP, Hôpital Bicêtre, Service de Rhumatologie, Centre de Référence Maladies Auto-Immunes et Systémiques Rares d'Île-de-France, Inserm UMR 1184, Center for Immunology of Viral Infections and Autoimmune Diseases, Université Paris-Saclay, Le Kremlin-Bicêtre, France.
  • Molto A; Centre de Recherche Epidémiologie et Biostatistiques de Sorbonne Paris Cité, Université de Paris, Paris, France; APHP, Hôpital Cochin, Service de Rhumatologie, Centre de Référence Maladies Auto-Immunes et Systémiques Rares d'Île-de-France, Paris, France.
  • Goulenok T; APHP, Hôpital Bichat, Service de Médecine Interne, Paris, France.
  • Diot E; CHU de Tours, Service de Médecine Interne, Tours, France.
  • Perard L; Hôpital Saint-Joseph, Service de Médecine Interne, Lyon, France.
  • Ferreira-Maldent N; CHU de Tours, Service de Médecine Interne, Tours, France.
  • Le Besnerais M; CHU de Rouen, Service de Médecine Interne, Rouen, France.
  • Limal N; APHP, Hôpital Henri-Mondor, Service de Médecine Interne, Créteil, France.
  • Martis N; CHU de Nice, Hôpital Archet, Service de Médecine Interne, Nice, France.
  • Abisror N; APHP, Hôpital Saint-Antoine, Service de Médecine Interne, Paris, France.
  • Debouverie O; CHU de Poitiers, Service de Médecine Interne, Poitiers, France.
  • Richez C; CHU de Bordeaux, Service de Rhumatologie, Bordeaux, France.
  • Sobanski V; CHU de Lille, Service de Médecine Interne et Immunologie Clinique, Centre de Référence des Maladies Auto-Immunes Systémiques Rares, Inserm U1286, Université de Lille, Lille, France.
  • Maurier F; Hôpitaux Privés de Metz, Service de Médecine Interne, Metz, France.
  • Sauvetre G; CHU de Rouen, Service de Médecine Interne, Rouen, France.
  • Levesque H; CHU de Rouen, Service de Médecine Interne, Rouen, France.
  • Timsit MA; CHU de Brest, Service de Rhumatologie, Brest, France.
  • Tieulié N; CHU de Nice, Service de Rhumatologie, Nice, France.
  • Orquevaux P; CHU de Reims, Service de Médecine Interne, Reims, France.
  • Bienvenu B; Hôpital Saint-Joseph, Service de Médecine Interne, Marseille, France.
  • Mahevas M; APHP, Hôpital Henri-Mondor, Service de Médecine Interne, Créteil, France.
  • Papo T; APHP, Hôpital Bichat, Service de Médecine Interne, Paris, France.
  • Lartigau-Roussin C; Hôpital Ouest Réunion, Service de Médecine Interne, Saint-Paul, la Réunion, France.
  • Chauvet E; Polyclinique Médipôle Saint-Roch, Service de Médecine Interne, Cabestany, France.
  • Berthoux E; Hôpital Saint-Joseph, Service de Médecine Interne, Lyon, France.
  • Sarrot-Reynauld F; CHU de Grenoble, Service de Médecine Interne, Grenoble, France.
  • Raffray L; CHU Félix-Guyon, Service de Médecine Interne, Saint-Denis de la Réunion, France.
  • Couderc M; CHU de Clermont-Ferrand, Service de Rhumatologie, Clermont-Ferrand, France.
  • Silva NM; CHU de Caen, Service de Médecine Interne, Caen, France.
  • Jourde-Chiche N; APHM, CHU de la Conception, Centre de Néphrologie et Transplantation Rénale, C2VN, Inserm 1263, Institut National de la Recherche Agronomique (INRA) 1260, Faculté de Pharmacie, Marseille, France.
  • Belhomme N; CHU de Rennes, Service de Médecine Interne, Rennes, France.
  • Thomas T; CHU de Saint-Etienne, Service de Médecine Interne, Saint-Etienne, France.
  • Poindron V; CHU de Strasbourg, Service de Médecine Interne, Strasbourg, France.
  • Queyrel-Moranne V; CHU de Nice, Hôpital Archet, Service de Médecine Interne, Nice, France.
  • Delforge J; APHP, Hôpital Jean-Verdier, Service de Médecine Interne, Bobigny, France.
  • Le Ray C; INSERM UMR 1153, Obstetrical, Perinatal and Pediatric Epidemiology Research Team (Epopé), Center for Epidemiology and Statistics, FHU PREMA, Université Paris Cité, Paris, France.
  • Pannier E; APHP, Hôpital Cochin Port Royal, Maternité Port Royal, Service d'Obstétrique, Université de Paris, Paris, France.
  • Mariette X; APHP, Hôpital Bicêtre, Service de Rhumatologie, Centre de Référence Maladies Auto-Immunes et Systémiques Rares d'Île-de-France, Inserm UMR 1184, Center for Immunology of Viral Infections and Autoimmune Diseases, Université Paris-Saclay, Le Kremlin-Bicêtre, France.
  • Le Guern V; APHP, Hôpital Cochin, Service de Médecine Interne, Centre de Référence Maladies Auto-Immunes et Systémiques Rares d'Île-de-France, Paris, France.
  • Seror R; APHP, Hôpital Bicêtre, Service de Rhumatologie, Centre de Référence Maladies Auto-Immunes et Systémiques Rares d'Île-de-France, Inserm UMR 1184, Center for Immunology of Viral Infections and Autoimmune Diseases, Université Paris-Saclay, Le Kremlin-Bicêtre, France. Electronic address: raphaele.seror@
Lancet Rheumatol ; 5(6): e330-e340, 2023 Jun.
Article em En | MEDLINE | ID: mdl-38251600
ABSTRACT

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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Resultado da Gravidez / Síndrome de Sjogren Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Newborn / Pregnancy Idioma: En Revista: Lancet Rheumatol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Resultado da Gravidez / Síndrome de Sjogren Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Newborn / Pregnancy Idioma: En Revista: Lancet Rheumatol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: França