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特发性脊柱侧凸中的血小板聚集异常。

Platelet aggregation abnormalities in idiopathic scoliosis.

作者信息

Sabato S, Rotman A, Robin G C, Floman Y

出版信息

J Pediatr Orthop. 1985 Sep-Oct;5(5):558-63. doi: 10.1097/01241398-198509000-00010.

Abstract

Platelet aggregation studies were performed in 22 adolescent girls with idiopathic scoliosis. Impaired ADP-induced platelet aggregation was found in washed platelets of the 22 patients with idiopathic scoliosis when compared with the controls (76.5% of control values; p less than 0.01). Furthermore, platelets from patients with progressive curves showed a greater degree of abnormality than platelets from those with nonprogressive curves, e.g., 57.6 +/- 22% of control values (p less than 0.001). No significant differences in aggregation could be detected when platelets were aggregated with the ionophore A-23187 in either the absence or the presence of calcium. Platelet aggregation studies in patients with other spinal deformities did not differ from the healthy controls. Because platelets share similar contractile proteins as muscles, the present study suggests that a muscle disorder may play an important pathogenic role in idiopathic scoliosis.

摘要

对22名患有特发性脊柱侧凸的青春期女孩进行了血小板聚集研究。与对照组相比,在22例特发性脊柱侧凸患者的洗涤血小板中发现二磷酸腺苷(ADP)诱导的血小板聚集受损(为对照值的76.5%;p<0.01)。此外,与非进展性侧弯患者的血小板相比,进展性侧弯患者的血小板显示出更高程度的异常,例如为对照值的57.6±22%(p<0.001)。当血小板在不存在或存在钙的情况下与离子载体A-23187聚集时,未检测到聚集的显著差异。其他脊柱畸形患者的血小板聚集研究与健康对照组无差异。由于血小板与肌肉共享相似的收缩蛋白,本研究表明肌肉疾病可能在特发性脊柱侧凸中起重要的致病作用。

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