Outcome of Pregnancy in Italian Patients with Primary Sjogren Syndrome

被引:31
|
作者
Priori, Roberta [1 ]
Gattamelata, Angelica [1 ]
Modesti, Mariagrazia [1 ]
Colafrancesco, Serena [1 ]
Frisenda, Silvia [1 ]
Minniti, Antonina [1 ]
Framarino-dei-Malatesta, Marialuisa [2 ]
Maset, Marta [3 ]
Quartuccio, Luca [3 ]
De Vita, Salvatore [3 ]
Bartoloni, Elena [4 ]
Alunno, Alessia [4 ]
Gerli, Roberto [4 ]
Strigini, Francesca [5 ]
Baldini, Chiara [6 ]
Tani, Chiara [6 ]
Mosca, Marta [6 ]
Bombardieri, Stefano [6 ]
Valesini, Guido [1 ]
机构
[1] Sapienza Univ, Rheumatol Unit, Rome, Italy
[2] Sapienza Univ, Dept Gynecol & Obstet, Rome, Italy
[3] Univ Udine, DSMB, Rheumatol Clin, I-33100 Udine, Italy
[4] Univ Perugia, Rheumatol Unit, Dept Clin & Expt Med, I-06100 Perugia, Italy
[5] Univ Pisa, Gynecol Unit, Pisa, Italy
[6] Univ Pisa, Rheumatol Unit, Pisa, Italy
关键词
SJOGREN SYNDROME; PREGNANCY; NEONATAL LUPUS; ABORTION; ANTI-RO/LA ANTIBODIES; SYSTEMIC-LUPUS-ERYTHEMATOSUS; DISEASE; WOMEN; RISK; MANIFESTATIONS; CLASSIFICATION; CRITERIA;
D O I
10.3899/jrheum.121518
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. To investigate pregnancy and fetal outcomes in patients with primary Sjogren syndrome (pSS). Methods. An obstetric history of 36 women with established diagnosis of pSS at pregnancy was obtained from a multicenter cohort of 1075 patients. In a subgroup case-control analysis, 12 deliveries in patients with pSS were compared with 96 control deliveries. Results. Thirty-six women (31 with anti-SSA/Ro and/or anti-SSB/La antibodies) with an established diagnosis of pSS had 45 pregnancies with the delivery of 40 newborns. Two miscarriages, 2 fetal deaths, and 1 induced abortion were recorded. Mean age at the first pregnancy was 33.9 years; mean number of pregnancies was 1.25; 18/40 (45%) cesarean births were delivered; mean pregnancy length was 38.5 weeks (range 32-43), with 6 preterm deliveries. The mean Apgar score at 5 min was 8.9, mean birthweight was 2920 g (range 826-4060 g). Congenital heart block (CHB) occurred in 2/40 (5%) newborns. The reported rate of breastfeeding for at least 1 month was 60.5%. In 4/40 pregnancies (10%) a flare of disease activity was observed within a year from delivery. In the case-control subgroup analysis, 12 deliveries were compared with 96 controls and no significant differences were found. Conclusion. Patients with pSS can have successful pregnancies, which might be followed by a mild relapse. CHB was the only cause of death for offspring of mothers with pSS.
引用
收藏
页码:1143 / 1147
页数:5
相关论文
共 50 条
  • [1] Critical overview of outcome parameters for patients with primary Sjogren's syndrome
    Feist, E.
    Hansen, A. A.
    ZEITSCHRIFT FUR RHEUMATOLOGIE, 2010, 69 (01): : 25 - +
  • [2] The impact of primary Sjogren's syndrome on pregnancy outcome: Our series and review of the literature
    De Carolis, Sara
    Salvi, Silvia
    Botta, Angela
    Garofalo, Serafina
    Garufi, Cristina
    Ferrazzani, Sergio
    De Carolis, Maria Pia
    AUTOIMMUNITY REVIEWS, 2014, 13 (02) : 103 - 107
  • [3] Hypocomplementemia in primary Sjogren's syndrome: association with serological, clinical features, and outcome
    Lin, Wei
    Xin, Zhifei
    Wang, Jialan
    Ren, Xiuying
    Liu, Yixuan
    Yang, Liu
    Guo, Shaoying
    Yang, Yupeng
    Li, Yang
    Cao, Jingjing
    Ning, Xiaoran
    Liu, Meilu
    Su, Yashuang
    Sun, Lijun
    Zhang, Fengxiao
    Zhang, Wen
    CLINICAL RHEUMATOLOGY, 2022, 41 (07) : 2091 - 2102
  • [4] Primary Sjogren's syndrome and pregnancy: A report of 18 cases
    Demarchi, Julia
    Papasidero, Silvia B.
    Klajn, Diana
    Alba, Paula
    Babini, Alejandra M.
    Durigan, Virginia
    Gobbi, Carla
    Raiti, Laura
    REUMATOLOGIA CLINICA, 2019, 15 (02): : 109 - 112
  • [5] Constrictive Bronchiolitis in Patients With Primary Sjogren Syndrome
    Wight, Elizabeth C.
    Baqir, Misbah
    Ryu, Jay H.
    JCR-JOURNAL OF CLINICAL RHEUMATOLOGY, 2019, 25 (02) : 74 - 77
  • [6] Primary Sjogren's Syndrome as a Systemic Disease: A Study of Participants Enrolled in an International Sjogren's Syndrome Registry
    Malladi, Arundathi S.
    Sack, Kenneth E.
    Shiboski, Stephen C.
    Shiboski, Caroline H.
    Baer, Alan N.
    Banushree, Ratukondla
    Dong, Yi
    Helin, Pekka
    Kirkham, Bruce W.
    Li, Mengtao
    Sugai, Susumu
    Umehara, Hisanori
    Vivino, Frederick B.
    Vollenweider, Cristina F.
    Zhang, Wen
    Zhao, Yan
    Greenspan, John S.
    Daniels, Troy E.
    Criswell, Lindsey A.
    ARTHRITIS CARE & RESEARCH, 2012, 64 (06) : 911 - 918
  • [7] Outcome measures for primary Sjogren's syndrome
    Seror, Raphaele
    Bootsma, Hendrika
    Bowman, Simon J.
    Doerner, Thomas
    Gottenberg, Jacques-Eric
    Mariette, Xavier
    Ramos-Casals, Manel
    Ravaud, Philippe
    Theander, Elke
    Tzioufas, Athanasios
    Vitali, Claudio
    JOURNAL OF AUTOIMMUNITY, 2012, 39 (1-2) : 97 - 102
  • [8] Long-term clinical course and outcome in patients with primary Sjogren syndrome-associated interstitial lung disease
    Kim, Yun Jae
    Choe, Jooae
    Kim, Ho Jeong
    Song, Jin Woo
    SCIENTIFIC REPORTS, 2021, 11 (01)
  • [9] Neurophysiological Features of Peripheral Nervous System Involvement and Immunological Profile of Patients with Primary Sjogren Syndrome
    Perzynska-Mazan, Joanna
    Maslinska, Maria
    Gasik, Robert
    JOURNAL OF RHEUMATOLOGY, 2020, 47 (11) : 1661 - 1667
  • [10] Prevalence and clinical impact of fibromyalgia in patients with primary Sjogren's syndrome
    Choi, B. Y.
    Oh, H. J.
    Lee, Y. J.
    Song, Y. W.
    CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, 2016, 34 (02) : S9 - S13