Analyses of Factors Influencing the Acute Effect of Octreotide in Growth Hormone-secreting Adenomas

被引:14
作者
Nakashima, Michi [1 ]
Takano, Koji [2 ]
Matsuno, Akira [1 ]
机构
[1] Teikyo Univ, Med Ctr, Dept Neurosurg, Ichihara, Chiba 2990111, Japan
[2] Univ Tokyo, Fac Med, Dept Nephrol & Endocrinol, Bunkyo Ku, Tokyo 1138655, Japan
关键词
Somatostatin receptor type 2A; Ki-67 staining index; Gsp mutation; Octreotide; GH-secreting adenoma; HUMAN SOMATOTROPH ADENOMAS; PITUITARY-TUMORS; SOMATOSTATIN ANALOGS; ACROMEGALIC PATIENTS; BIOCHEMICAL CHARACTERISTICS; ADENYLYL-CYCLASE; GSP MUTATIONS; IN-VITRO; EXPRESSION; G(S)ALPHA;
D O I
10.1507/endocrj.K08E-305
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Somatostatin analogues such as octreotide are used to treat active acromegalic patients by reducing serum growth hormone (GH) levels. However, the acute effect of octreotide oil GH secretion differs among patients. To elucidate factors influencing the acute effect of octreotide, we collected data front 56 patients with somatotroph adenoma from two institutions. We analyzed the correlation of the following factors with the acute effect of octreotide: immunohistochemical staining of somatostatin receptor subtype 2A (SSTR 2A), presence of gsp mutation, proliferative potentials analyzed by Ki-67 staining index (SI). We found that the acute effect of octreotide significantly correlated with two factors: Ki-67 SI and the plasma membrane-dominant staining pattern of SSTR 2A. Monovariate analysis revealed a statistically significant inverse relation of Ki-67 SI with the reduction of GH by octreotide. We assessed the contribution of each factor on the acute effect of octreotide by multivariate analysis. Significant multiple regression was confirmed with p value of 0.003. Post-test revealed that the plasma membrane-dominant staining pattern of SSTR 2A was significantly related to the reduction of GH by octreotide. These results show that the acute effect of octreotide is positively related to SSTR 2A staining on the plasma membrane.
引用
收藏
页码:295 / 304
页数:10
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