Yasufuku-Takano Junko, Takano Koji, Morita Koji, Takakura Kintomo, Teramoto Akira, Fujita Toshiro
Department of Nephrology and Endocrinology, University of Tokyo School of Medicine, Faculty of Medicine, Bunkyo-ku, Tokyo 113-8655, Japan.
Clin Endocrinol (Oxf). 2006 Jan;64(1):91-6. doi: 10.1111/j.1365-2265.2005.02423.x.
The prevalence of gsp mutations in GH-secreting pituitary adenomas was thought to differ geographically or racially, given its exceptionally lower incidence among Japanese patients (4.4-9.3%) compared to other regions (30-50%). However, this notion is now being challenged after a recent paper reported a 53.3% incidence among Japanese with acromegaly. We have since re-evaluated the prevalence of gsp mutations on a larger scale.
One hundred Japanese acromegaly patients with surgically confirmed GH-secreting pituitary adenomas were enrolled.
mRNAs from primary cultured adenomas were used for reverse transcriptase-polymerase chain reaction and direct sequencing of the Gsalpha subunit. Patient data were reviewed from medical charts.
There were 53 gsp mutations (53%), consisting of 42 Arg201Cys, one Arg201His, one Arg201Ser, 8 Gln227Leu, and one Gln227Arg mutation. Age at operation, sex ratio, basal serum GH and IGF-I levels were no different with or without the mutations. In contrast, patients responded differently to most dynamic tests with statistical significance: serum GH levels in gsp-positive patients had blunted response to GHRH, were well suppressed by bromocriptine, and had higher rates of paradoxical response to TRH. Notably, paradoxical response to LHRH was observed exclusively in gsp-negative patients. Octreotide suppressed GH levels strongly regardless of gsp status. These clinical characteristics are similar to those of Caucasian patients.
We conclude that the prevalence of gsp mutations in Japanese acromegaly patients is comparable to those of other reports from various regions. Therefore, Japanese patients do not stand as an example for geographical or racial difference in the prevalence of gsp mutations in GH-secreting pituitary adenomas.
鉴于生长激素分泌型垂体腺瘤中gsp突变的发生率在日本患者中(4.4 - 9.3%)异常低于其他地区(30 - 50%),人们认为其在地理或种族上存在差异。然而,最近一篇论文报道日本肢端肥大症患者中该突变发生率为53.3%,这一观点目前正受到挑战。此后,我们对gsp突变的发生率进行了更大规模的重新评估。
招募了100例经手术确诊为生长激素分泌型垂体腺瘤的日本肢端肥大症患者。
将原代培养腺瘤的mRNA用于逆转录聚合酶链反应及Gsα亚基的直接测序。从病历中回顾患者数据。
共有53例gsp突变(53%),包括42例Arg201Cys、1例Arg201His、1例Arg201Ser、8例Gln227Leu和1例Gln227Arg突变。有或无突变患者的手术年龄、性别比例、基础血清生长激素和胰岛素样生长因子 - I水平无差异。相比之下,患者对大多数动态试验的反应在统计学上有显著差异:gsp阳性患者的血清生长激素水平对生长激素释放激素反应迟钝,被溴隐亭良好抑制,对促甲状腺激素释放激素的反常反应发生率更高。值得注意的是,仅在gsp阴性患者中观察到对促黄体生成素释放激素的反常反应。无论gsp状态如何,奥曲肽均能强烈抑制生长激素水平。这些临床特征与白种人患者相似。
我们得出结论,日本肢端肥大症患者中gsp突变的发生率与其他不同地区的报道相当。因此,在生长激素分泌型垂体腺瘤中,日本患者不能作为gsp突变发生率存在地理或种族差异的例证。