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格雷夫斯病患者血清中可溶性细胞间黏附分子-1(ICAM-1)的纵向研究。

Longitudinal study of soluble intercellular adhesion molecule-1 (ICAM-1) in sera of patients with Graves' disease.

作者信息

Sonnet E, Massart C, Gibassier J, Allannic H, Maugendre D

机构信息

Service d'Endocrinologie, Centre Hospitalier Universitaire de Rennes, France.

出版信息

J Endocrinol Invest. 1999 Jun;22(6):430-5. doi: 10.1007/BF03343586.

Abstract

Adhesion molecules, such as Intercellular Adhesion Molecule-1 (ICAM-1), play an important role during the autoimmune process of Graves' disease (GD). So the objective of the study was to evaluate the time-course of the soluble ICAM-1 (sICAM-1) in GD. Concentrations of sICAM-1, thyroid hormones and TSAb (thyroid-stimulating antibodies) were determined in sera from 30 healthy controls, 41 untreated GD patients and after 3, 6, 12, 18 months of carbimazole therapy (no.=30), at relapse (no.=11) or 2 years after the end of therapy when remission (no.=13). Mean sICAM-1 concentration was significantly higher in untreated GD patients than in controls (mean+/-SD: 371+/-108 ng/ml vs 243+/-47 ng/ml, p<0.0001) until 6 months of therapy (289+/-102 ng/ml; NS). The number of positive patients (sICAM-1 levels>mean of the controls+2 SD) declined from 56% (23/41) at the time of the diagnosis to 10% (3/29) at 18 months. At relapse, mean sICAM-1 level significantly increased compared to that at 18 months of therapy (288+/-65 vs 236+/-59 ng/ml, p=0.005). At remission mean sICAM-1 level was significantly lower than in relapse patients (240+/-48 ng/ml, p=0.04); no patient displayed sICAM-1 positive values. In conclusion, sICAM-1 concentrations were increased in sera of newly diagnosed GD patients, declined significantly during carbimazole therapy and could again be increased at relapse. sICAM-1 could reflect an ongoing immune process and help to affirm the presence of an autoimmunity notably in some cases of TSAb negative patients. However its precise interest in clinical practice remains to be determined in further studies.

摘要

黏附分子,如细胞间黏附分子-1(ICAM-1),在格雷夫斯病(GD)的自身免疫过程中发挥重要作用。因此,本研究的目的是评估GD患者可溶性ICAM-1(sICAM-1)的时间进程。测定了30名健康对照者、41名未经治疗的GD患者以及在接受卡比马唑治疗3、6、12、18个月后(n = 30)、复发时(n = 11)或治疗结束2年后缓解期(n = 13)患者血清中sICAM-1、甲状腺激素和TSAb(促甲状腺素抗体)的浓度。未经治疗的GD患者血清中sICAM-1的平均浓度显著高于对照组(均值±标准差:371±108 ng/ml对243±47 ng/ml,p<0.0001),直至治疗6个月时(289±102 ng/ml;无显著性差异)。阳性患者(sICAM-1水平>对照组均值+2个标准差)的数量从诊断时的56%(23/41)降至18个月时的10%(3/29)。复发时,sICAM-1的平均水平与治疗18个月时相比显著升高(288±65对236±59 ng/ml,p = 0.005)。缓解期sICAM-1的平均水平显著低于复发患者(240±48 ng/ml,p = 0.04);无患者sICAM-1呈阳性值。总之,新诊断的GD患者血清中sICAM-1浓度升高,在卡比马唑治疗期间显著下降,复发时可能再次升高。sICAM-1可以反映正在进行的免疫过程,并有助于明确自身免疫的存在,特别是在一些TSAb阴性患者中。然而,其在临床实践中的确切意义仍有待进一步研究确定。

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