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Serological autoimmune profile of systemic lupus erythematosus in deep and non-deep endometriosis patients
被引:1
作者:
Coloma, J. L.
[1
]
Martinez-Zamora
[1
]
Tassies, D.
[2
]
Reverter, J. C.
[2
]
Espinosa, G.
[3
]
Cervera, R.
[3
]
Carmona, F.
[1
]
机构:
[1] Univ Barcelona, Hosp Clin Barcelona, Inst Invest Biomed August Pi i Sunyer IDIBAPS, Fac Med,Inst Clin Gynaecol Obstet & Neonatol,Dept, Villarroel 170, Barcelona 08036, Spain
[2] Hosp Clin Barcelona, Dept Hemotherapy & Hemostasis, Villarroel 170, Barcelona 08036, Spain
[3] Hosp Clin Barcelona, Dept Autoimmune Dis, Villarroel 170, Barcelona 08036, Spain
关键词:
Endometriosis;
Autoimmunity;
Antinuclear antibodies;
Pain;
arthralgia;
Asthenia;
CARDIOLIPIN ANTIBODY-LEVELS;
ANTINUCLEAR ANTIBODIES;
DISEASES;
WOMEN;
PATHOGENESIS;
PREVALENCE;
RISK;
D O I:
10.1016/j.jri.2023.103827
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Objective: Several studies have reported a high prevalence of autoimmune diseases such as systemic lupus ery-thematosus (SLE) in endometriosis patients. The aim of this study was to evaluate the SLE autoimmune antibody profile in patients with deep (DE) and non-deep endometriosis (Non-DE).Materials and methods: Four groups of premenopausal patients were evaluated: patients with DE (n = 50); pa-tients with ovarian endometriomas (Non-DE; n = 50); healthy patients without endometriosis (C group; n = 45); and SLE patients without endometriosis (SLE group; N = 46). Blood samples were obtained and the standard SLE autoimmune profile was evaluated in all patients. Pain symptoms related to endometriosis and clinical SLE manifestations were also recorded.Results: The DE group presented a statistically significant higher proportion of patients with antinuclear anti-bodies (ANA) (20%) compared to the Non-DE group (4%) and C group (2.2%). Levels of complement were more frequently lower among DE and Non-DE patients although differences did not reach statistical significance. Similarly, anti-dsDNA antibodies and anticoagulant lupus were positive in more patients of the DE group but did not reach statistical significance. The DE group complained of more arthralgia and asthenia compared to the Non-DE and C groups.Conclusions: The results of this study showed higher positivity of ANA and greater arthralgia and asthenia in patients with DE compared with Non-DE patients and healthy controls, suggesting that they may have a higher susceptibility to autoimmune diseases and present more generalized pain.
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