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Redistribution of cellular mineral and trace element stores in HLA-B27 positive relatives of patients with ankylosing spondylitis--a marker of hidden inflammatory disease.

作者信息

Feltelius N, Hällgren R, Lindh U

机构信息

Department of Internal Medicine, University Hospital, Uppsala, Sweden.

出版信息

J Rheumatol. 1988 Feb;15(2):308-14.

PMID:3258920
Abstract

Subjectively healthy HLA-B27 positive 1st degree relatives (n = 14) of patients with ankylosing spondylitis (AS) were investigated concerning the mass fraction of calcium (Ca), magnesium (Mg), manganese (Mn), iron (Fe), zinc (Zn), strontium (Sr) and copper (Cu) in isolated blood cells using the nuclear microprobe technique. No relative had laboratory signs of inflammatory disease defined by acute phase plasma proteins. An accumulation of Mg, Ca, Mn and Fe was found in granulocytes compared with healthy controls. In platelets there was an accumulation of Fe and a reduction of the Cu content. In erythrocytes Ca was accumulated and the levels of Mg, Mn and Cu were reduced compared with the controls. Five of the relatives had radiological signs of sacroiliitis and 1 of these had sacroiliac tenderness. Relatives with and without radiological sacroiliitis showed no differences in the cellular metal amounts. When the alterations were compared with those previously found in patients with AS, a striking similarity was noted, although the changes were quantitatively less pronounced. In contrast B27 negative 1st degree relatives (n = 11) had normal mineral amounts in their cells. However, it seems less likely that altered metal handling could play a primary role for the disease susceptibility linked to HLA-B27 since B27 positive healthy controls (n = 12) without AS in the family had normal cellular stores of the measured elements. Rather our findings indicate that redistribution of cellular metals is an extremely sensitive marker of an inflammatory process not evident by clinical symptoms or increase of acute phase plasma proteins.

摘要

相似文献

1
Redistribution of cellular mineral and trace element stores in HLA-B27 positive relatives of patients with ankylosing spondylitis--a marker of hidden inflammatory disease.
J Rheumatol. 1988 Feb;15(2):308-14.
2
Redistribution of minerals and trace elements in chronic inflammation--a study on isolated blood cells from patients with ankylosing spondylitis.
J Rheumatol. 1987 Jun;14(3):548-53.
3
Symptoms and signs among relatives of patients with HLA B27 ankylosing spondylitis: Correlation between back pain, spinal movement, sacroilitis, and HLA antigens.HLA B27 强直性脊柱炎患者亲属的症状和体征:背痛、脊柱活动、骶髂关节炎与 HLA 抗原之间的相关性。
J Rheumatol Suppl. 1977;3:11-7.
4
The risk of sacroiliitis in B27 positive persons: a reappraisal.B27 阳性人群中骶髂关节炎的风险:重新评估
J Rheumatol. 1984 Jun;11(3):327-9.
5
TNF-238A promoter polymorphism contributes to susceptibility to ankylosing spondylitis in HLA-B27 negative patients.TNF-238A启动子多态性导致HLA-B27阴性患者易患强直性脊柱炎。
J Rheumatol. 2001 Jun;28(6):1288-93.
6
HLA B27 and ankylosing spondylitis: a population and family study in Sardinia.人类白细胞抗原B27与强直性脊柱炎:撒丁岛的一项人群及家族研究
J Rheumatol Suppl. 1977;3:18-23.
7
[Ankylosing spondylitis (Bechterew) and tissue antigen HLA-B27. III, Heredity of ankylosing spondylitis (Bechterew)].[强直性脊柱炎(别赫捷列夫病)与组织抗原HLA - B27。III,强直性脊柱炎(别赫捷列夫病)的遗传]
Z Rheumatol. 1977 Jul-Aug;36(7-8):230-8.
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Ankylosing spondylitis: a family study.强直性脊柱炎:一项家族研究。
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Immune function in ankylosing spondylitics and their relatives: influence of disease and HLA B27.强直性脊柱炎患者及其亲属的免疫功能:疾病和HLA B27的影响。
Clin Exp Immunol. 1978 Aug;33(2):270-5.
10
HLA antigens in seronegative spondylarthropathies. Reactive arthritis and arthritis in ankylosing spondylitis: relation to gut inflammation.
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引用本文的文献

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No evidence of a genetic causal relationship between ankylosing spondylitis and iron homeostasis: A two-sample Mendelian randomization study.强直性脊柱炎与铁稳态之间不存在遗传因果关系的证据:一项两样本孟德尔随机化研究。
Front Nutr. 2023 Mar 23;10:1047640. doi: 10.3389/fnut.2023.1047640. eCollection 2023.
2
Metal content of neutrophil granules is altered in chronic inflammation.在慢性炎症中,中性粒细胞颗粒的金属含量会发生改变。
Inflammation. 1989 Aug;13(4):383-92. doi: 10.1007/BF00914922.