Publication:
Ovarian function and reproductive outcomes of female patients with systemic lupus erythematosus and the strategies to preserve their fertility

dc.contributor.coauthorGuzel, Yilmaz
dc.contributor.coauthorAksoy, Senai
dc.contributor.coauthorAydin, Elvin
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorÖktem, Özgür
dc.contributor.kuauthorUrman, Cumhur Bülent
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-11-09T23:20:01Z
dc.date.issued2015
dc.description.abstractSystemic lupus erythematosus (SLE) is a chronic autoimmune systemic disease that mainly affects women of reproductive age. Emerging data from recent molecular studies show us that estrogen hormone plays a central role in the development of this disease. By acting via its cognate receptors ER alpha and ER beta expressed on immune cells, estrogen can modulate immune function in both the innate and adaptive immune responses. Interestingly, estrogen may also evoke autoimmune responses after binding to B lymphocytes leading to the generation of high-affinity autoantibodies and proinflammatory cytokines (so-called estrogen-induced autoimmunity). Unfortunately, reproductive function of young female patients with this disease is commonly compromised by different pathophysiologic processes. First, ovarian reserve is diminished even in the presence of mild disease suggesting a direct impact of the disease itself on ovarian function possibly due to ovarian involvement in the form of autoimmune oophoritis. Second, SLE patients with severe manifestations of the disease are treated with alkylating chemotherapy agent cyclophosphamide. Cyclophosphamide and other drugs of alkylating category have the highest gonadotoxicity. Therefore, SLE patients exposed to cyclophosphamide have a much higher risk of developing infertility and premature ovarian failure than do the counterparts who are treated with other less toxic treatments. Third, the functions of the hypothalamic pituitary ovarian axis are perturbed by chronic inflammatory state. and finally adverse pregnancy outcomes are more commonly observed in SLE patients such as fetal loss, preterm birth, intrauterine fetal growth restriction, preeclampsia-eclampsia, and fetal congenital heart block. We aimed in this review article to provide the readers an update on how estrogen hormone closely interacts with and induces lupus-prone changes in the immune system. We also discuss ovarian function and other reproductive outcomes in SLE patients and the current strategies to preserve their fertility in the light of the most recent evidence-based findings of the clinical trials and molecular studies. Target Audience: Obstetricians and gynecologists, family physicians
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue3
dc.description.openaccessNO
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.volume70
dc.identifier.doi10.1097/OGX.0000000000000160
dc.identifier.eissn1533-9866
dc.identifier.issn0029-7828
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-84924974317
dc.identifier.urihttps://doi.org/10.1097/OGX.0000000000000160
dc.identifier.urihttps://hdl.handle.net/20.500.14288/10649
dc.identifier.wos351009800019
dc.keywordsAnti-mullerian hormone
dc.keywordsBreast-cancer chemotherapy
dc.keywordsMultiethnic us cohort
dc.keywordsPremenopausal women
dc.keywordsDisease-activity
dc.keywordsMycophenolate-mofetil
dc.keywordsPregnancy outcomes
dc.keywordsOocyte cryopreservation
dc.keywordsCardiac manifestations
dc.keywordsGene polymorphisms
dc.language.isoeng
dc.publisherLippincott Williams and Wilkins
dc.relation.ispartofObstetrical & Gynecological Survey
dc.subjectObstetrics
dc.subjectGynecology
dc.titleOvarian function and reproductive outcomes of female patients with systemic lupus erythematosus and the strategies to preserve their fertility
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorÖktem, Özgür
local.contributor.kuauthorUrman, Cumhur Bülent
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit2School of Medicine
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relation.isOrgUnitOfPublication.latestForDiscoveryd02929e1-2a70-44f0-ae17-7819f587bedd
relation.isParentOrgUnitOfPublication17f2dc8e-6e54-4fa8-b5e0-d6415123a93e
relation.isParentOrgUnitOfPublication.latestForDiscovery17f2dc8e-6e54-4fa8-b5e0-d6415123a93e

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