Literature DB >> 18504280

Oestrogens in rheumatic diseases: friend or foe?

M Cutolo1, S Capellino, R H Straub.   

Abstract

Immunological and epidemiological evidences suggest that female sex hormones play an important role in the aetiology and pathophysiology of chronic inflammatory diseases; however, whether (or when) oestrogens are friends or foes in inflammatory/immune-mediated rheumatic diseases is still a matter of debate. Several significant factors generate confusion and opposite conclusions in evaluating the role of oestrogens in inflammatory/immune diseases. These factors include the relatively superficial translation done from the animal studies to the human condition, the different effects of oestrogens on their different receptors or on different target cells, the different oestrogen concentrations employed and finally, opposite effects (especially on cell proliferation) exerted by different peripheral oestrogen metabolites. However, as supported by the higher prevalence of rheumatic autoimmune diseases in women, oestrogens are generally considered as enhancers of cell proliferation and humoral immune response.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 18504280     DOI: 10.1093/rheumatology/ken150

Source DB:  PubMed          Journal:  Rheumatology (Oxford)        ISSN: 1462-0324            Impact factor:   7.580


  22 in total

1.  Oral contraceptives, reproductive factors and risk of inflammatory bowel disease.

Authors:  Hamed Khalili; Leslie M Higuchi; Ashwin N Ananthakrishnan; James M Richter; Diane Feskanich; Charles S Fuchs; Andrew T Chan
Journal:  Gut       Date:  2012-05-22       Impact factor: 23.059

2.  Association Between Long-term Oral Contraceptive Use and Risk of Crohn's Disease Complications in a Nationwide Study.

Authors:  Hamed Khalili; Fredrik Granath; Karin E Smedby; Anders Ekbom; Martin Neovius; Andrew T Chan; Ola Olen
Journal:  Gastroenterology       Date:  2016-02-23       Impact factor: 22.682

Review 3.  Pregnancy and rheumatoid arthritis: insights into the immunology of fetal tolerance and control of autoimmunity.

Authors:  Shreyasee Amin; Erik J Peterson; Ann M Reed; Daniel L Mueller
Journal:  Curr Rheumatol Rep       Date:  2011-10       Impact factor: 4.592

Review 4.  Smoking out reproductive hormone actions in lung cancer.

Authors:  Jill M Siegfried
Journal:  Mol Cancer Res       Date:  2014-01-07       Impact factor: 5.852

5.  Role of environmental factors in the pathogenesis of Crohn's disease: a critical review.

Authors:  Yueying Chen; Yining Wang; Jun Shen
Journal:  Int J Colorectal Dis       Date:  2019-11-16       Impact factor: 2.571

6.  Hormone therapy increases risk of ulcerative colitis but not Crohn's disease.

Authors:  Hamed Khalili; Leslie M Higuchi; Ashwin N Ananthakrishnan; JoAnn E Manson; Diane Feskanich; James M Richter; Charles S Fuchs; Andrew T Chan
Journal:  Gastroenterology       Date:  2012-07-27       Impact factor: 22.682

Review 7.  Risk of Inflammatory Bowel Disease with Oral Contraceptives and Menopausal Hormone Therapy: Current Evidence and Future Directions.

Authors:  Hamed Khalili
Journal:  Drug Saf       Date:  2016-03       Impact factor: 5.606

8.  Reproductive and hormonal risk factors for antinuclear antibodies (ANA) in a representative sample of U.S. women.

Authors:  Christine G Parks; Frederick W Miller; Minoru Satoh; Edward K L Chan; Zhanna Andrushchenko; Linda S Birnbaum; Todd A Jusko; Grace E Kissling; Mehul D Patel; Kathryn M Rose; Clarice Weinberg; Darryl C Zeldin; Dale P Sandler
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2014-08-01       Impact factor: 4.254

9.  Dermatomyositis onset in the puerperium period.

Authors:  Sofia Mateus; Mariana Malheiro; Miguel Perneta Santos; Rui Costa
Journal:  BMJ Case Rep       Date:  2015-09-11

Review 10.  Insights into endocrine-immunological disturbances in autoimmunity and their impact on treatment.

Authors:  Maurizio Cutolo; Rainer H Straub
Journal:  Arthritis Res Ther       Date:  2009-04-06       Impact factor: 5.156

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.