Rheumatic Diseases in Reproductive Age—the Possibilities and the Risks

被引:0
|
作者
Bogna Grygiel-Górniak
Elena Masiero
Briana Candace Nevaneeth
Melissa Mary Jojy
机构
[1] Poznan University of Medical Sciences,Department of Rheumatology, Rehabilitation and Internal Diseases
来源
Reproductive Sciences | 2023年 / 30卷
关键词
Rheumatic diseases; Pregnancy complications; Recommendations; Treatment during pregnancy;
D O I
暂无
中图分类号
学科分类号
摘要
The most common systemic connective tissue diseases (CTD), such as rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), antiphospholipid syndrome (APS), systemic sclerosis (SSc), and Sjögren’s syndrome (SjS), affect many women of reproductive age. These diseases may strongly impact the course of pregnancy and increase the risk factors of incompatibility. A literature search was done on MEDLINE, PubMed, and Google Scholar in 2011–2021. The analysis included meta-analysis, randomized control trials, prospective and retrospective studies, and systematic reviews. The literature search allowed us to form conclusions and underline recommendations regarding pregnancy’s risk and treatment possibilities in the course of rheumatic disease. Optimal control of CTD activity should be reached at least 6 months before conception. High-risk pregnancies are often accompanied by maternal-placental syndrome, which manifests as preeclampsia, eclampsia, fetal growth restriction, and prematurity. The flare of rheumatic disease can coexist with obstetrical complications, and differential diagnosis can be difficult. Medications that do not influence the risk of fetus complications should be applied before and during pregnancy. Teratogenic drugs (e.g., methotrexate, leflunomide, cyclophosphamide) must be withdrawn before pregnancy. Conventional medications such as hydroxychloroquine, sulfasalazine, colchicine, and the TNFα inhibitor certolizumab can be used safely at any stage of pregnancy. Corticosteroids should be tapered, and other biologics should be avoided due to teratogenicity or carefully administered due to the impact on the fetal immune system. Distinguishing between disease flare and obstetrical complications can be difficult in clinical practice; however, some clinical symptoms and serological markers can be helpful in the differential diagnosis.
引用
收藏
页码:111 / 123
页数:12
相关论文
共 50 条
  • [21] NETosis in Rheumatic Diseases
    Mehul P. Jariwala
    Ronald M. Laxer
    Current Rheumatology Reports, 2021, 23
  • [22] Osteoporosis in Rheumatic Diseases
    Adami, Giovanni
    Fassio, Angelo
    Rossini, Maurizio
    Caimmi, Cristian
    Giollo, Alessandro
    Orsolini, Giovanni
    Viapiana, Ombretta
    Gatti, Davide
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2019, 20 (23)
  • [23] Prevalence of Migraine and Neuropathic Pain in Rheumatic Diseases
    Mathieu, Sylvain
    Couderc, Marion
    Pereira, Bruno
    Dubost, Jean-Jacques
    Malochet-Guinamand, Sandrine
    Tournadre, Anne
    Soubrier, Martin
    Moisset, Xavier
    JOURNAL OF CLINICAL MEDICINE, 2020, 9 (06) : 1 - 13
  • [24] Osteoporosis in rheumatic diseases
    Li-Xia Gao
    Hong-Tao Jin
    Xiao-Mei Xue
    Jia Wang
    Dong-Gang Liu
    World Journal of Rheumatology, 2015, (01) : 23 - 35
  • [25] Frailty in Rheumatic Diseases
    Motta, Francesca
    Sica, Antonio
    Selmi, Carlo
    FRONTIERS IN IMMUNOLOGY, 2020, 11
  • [26] NETosis in Rheumatic Diseases
    Jariwala, Mehul P.
    Laxer, Ronald M.
    CURRENT RHEUMATOLOGY REPORTS, 2021, 23 (02)
  • [27] Osteoporosis and rheumatic diseases
    Maruotti, N.
    Corrado, A.
    Cantatore, F. P.
    REUMATISMO, 2014, 66 (02) : 125 - 135
  • [28] SELENIUM IN RHEUMATIC DISEASES
    PERETZ, AM
    NEVE, JD
    FAMAEY, JPP
    SEMINARS IN ARTHRITIS AND RHEUMATISM, 1991, 20 (05) : 305 - 316
  • [29] Chemokines in rheumatic diseases
    Szekanecz, Z
    Szücs, G
    Szántó, S
    Koch, AE
    CURRENT DRUG TARGETS, 2006, 7 (01) : 91 - 102
  • [30] Calprotectin in rheumatic diseases
    Ometto, Francesca
    Friso, Lara
    Astorri, Davide
    Botsios, Costantino
    Raffeiner, Bernd
    Punzi, Leonardo
    Doria, Andrea
    EXPERIMENTAL BIOLOGY AND MEDICINE, 2017, 242 (08) : 859 - 873