Li Yang , Yueqiu Shen , Minqin Xu , Ling Zhou , Hong Zhang
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引用次数: 0
Abstract
Whether hydroxychloroquine intervention can improve pregnancy outcomes in patients with recurrent pregnancy loss patients (RPL) with antinuclear antibodies (ANAs) positive is still unknown.
RPL patients who were positive for ANAs without rheumatism were recruited from the Reproductive Medicine Center of the Second Affiliated Hospital of Soochow University from January 2016 to December 2023 (N = 104). Normal healthy pregnant women were selected as the Control group (N = 100). ANA-positive pregnant women who had experienced one sporadic abortion were included in the SA group (N = 42). Patients in both RPL and SA groups received 0.2–0.4 g hydroxychloroquine daily. General data and pregnancy outcomes were compared among the three groups. Patients with RPL were divided into three subgroups according to ANA titers: 1:100 (n = 81), 1:320 (n = 18) and 1:1000 (n = 5). The differences in the pregnancy outcomes among the subgroups were compared.
We found the abortion rates in RPL and SA groups were greater than that in the control group (P < 0.05). The incidence of pregnancy complications was greater in the RPL group than in the control group (P < 0.05). The full-term live birth rates in RPL and SA groups were lower than that in the control group (P < 0.05). There were significant differences in the abortion rate among patients with RPL with different ANA titers (P < 0.05).
We concluded that adverse pregnancy outcomes, such as abortion and complications during pregnancy, are still more common in ANA-positive RPL patients than in normal pregnant women despite treatment. The ANA titer is closely related to the abortion rate among RPL patients during sequent pregnancy.
期刊介绍:
The journal''s scope includes understanding the genetic and functional mechanisms that distinguish human individuals in their immune responses to allografts, pregnancy, infections or vaccines as well as the immune responses that lead to autoimmunity, allergy or drug hypersensitivity. It also includes examining the distribution of the genes controlling these responses in populations.
Research areas include:
Studies of the genetics, genomics, polymorphism, evolution, and population distribution of immune-related genes
Studies of the expression, structure and function of the products of immune-related genes
Immunogenetics of susceptibility to infectious and autoimmune disease, and allergy
The role of the immune-related genes in hematopoietic stem cell, solid organ, and vascularized composite allograft transplant
Histocompatibility studies including alloantibodies, epitope definition, and T cell alloreactivity
Studies of immunologic tolerance and pregnancy
T cell, B cell, NK and regulatory cell functions, particularly related to subjects within the journal''s scope
Pharmacogenomics and vaccine development in the context of immune-related genes
Human Immunology considers immune-related genes to include those encoding classical and non-classical HLA, KIR, MIC, minor histocompatibility antigens (mHAg), immunoglobulins, TCR, BCR, proteins involved in antigen processing and presentation, complement, Fc receptors, chemokines and cytokines. Other immune-related genes may be considered.
Human Immunology is also interested in bioinformatics of immune-related genes and organizational topics impacting laboratory processes, organ allocation, clinical strategies, and registries related to autoimmunity and transplantation.