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散发性年轻肢端肥大症和垂体巨大症中的胚系 AIP 变异:来自汉族队列的临床和遗传见解。

Germline AIP variants in sporadic young acromegaly and pituitary gigantism: clinical and genetic insights from a Han Chinese cohort.

机构信息

Department of Endocrinology and Metabolism, Huashan Hospital, Fudan University, No. 12 Wulumuqi Middle Road, Shanghai, China.

Department of General Practice, Zhongshan Hospital, Fudan University, No.180 Fenglin Road, Shanghai, China.

出版信息

Endocrine. 2024 Sep;85(3):1346-1356. doi: 10.1007/s12020-024-03898-x. Epub 2024 Jun 8.

Abstract

PURPOSE

Variants in the Aryl hydrocarbon receptor-interacting protein (AIP) gene have been identified in sporadic acromegaly and pituitary gigantism, especially in young patients, with a predisposition to aggressive clinical phenotype and poor treatment efficacy. The clinical characteristics of patients with sporadic acromegaly and pituitary gigantism as well as AIP variants in Han Chinese have been rarely reported. We aimed to identify AIP gene variants and analyze the clinical characteristics of patients with sporadic acromegaly and pituitary gigantism in Han Chinese.

METHODS

The study included 181 sporadic acromegaly (N = 163) and pituitary gigantism (N = 18) patients with an onset age of no more than 45 years old, who were diagnosed, treated, and followed up in Huashan Hospital. All 6 exons and their flanking regions of the AIP gene were analyzed with Sanger sequencing or NGS. The clinical characteristics were compared between groups with and without AIP variants.

RESULTS

Germline AIP variants were found in 15/181 (8.29%) cases. In patients with an onset age ≤30 years old, AIP variants were identified in 12/133 (9.02%). Overall, 13 variants were detected. The pathogenic (P) variants p.R304X and p.R81X were identified in four cases, with two instances of each variant. Six exon variants (p.C254R, p.K103fs, p.Q228fs, p.Y38X, p.Q213*, and p.1115 fs) have not been reported before, which were likely pathogenic (LP). Patients with P/LP variants had younger onset ages, a higher prevalence of pituitary gigantism, larger tumor volumes, and a higher percentage of Ki-67-positive cells in tumors. In addition, the group with P/LP variants showed a less significant reduction of GH levels in an acute octreotide suppression test (OST) [17.7% (0, 65.0%) vs. 80.5% (63.9%, 90.2%), P = 0.001], and a trend of less GH decrease after the 3-month treatment with long-acting somatostatin analogs (SSAs).

CONCLUSION

Germline AIP variants existed in sporadic Chinese Han acromegaly and pituitary gigantism patients and were more likely to be detected in young patients. AIP variants were associated with more aggressive tumor phenotypes and less response to SSA treatment.

摘要

目的

芳香烃受体相互作用蛋白(AIP)基因中的变异已在散发型肢端肥大症和垂体巨人症中被发现,尤其是在年轻患者中,这些患者具有侵袭性临床表型和较差的治疗效果的倾向。在中国汉族人群中,散发型肢端肥大症和垂体巨人症患者的临床特征以及 AIP 变异的报道很少。我们旨在鉴定 AIP 基因变异,并分析中国汉族散发型肢端肥大症和垂体巨人症患者的临床特征。

方法

该研究纳入了 181 例发病年龄不超过 45 岁的散发型肢端肥大症(N=163)和垂体巨人症(N=18)患者,这些患者均在华山医院被诊断、治疗和随访。采用 Sanger 测序或 NGS 分析 AIP 基因的 6 个外显子及其侧翼区。比较有和无 AIP 变异的患者之间的临床特征。

结果

在 181 例患者中发现了 15 例(8.29%)种系 AIP 变异。在发病年龄≤30 岁的患者中,在 133 例患者中发现了 12 例(9.02%)AIP 变异。总共检测到 13 种变异。致病性(P)变异 p.R304X 和 p.R81X 在 4 例患者中被发现,各有 2 例。6 种外显子变异(p.C254R、p.K103fs、p.Q228fs、p.Y38X、p.Q213* 和 p.1115fs)以前未被报道过,这些变异可能是致病性的(LP)。携带 P/LP 变异的患者发病年龄较小,垂体巨人症患病率较高,肿瘤体积较大,肿瘤中 Ki-67 阳性细胞的比例较高。此外,在奥曲肽急性抑制试验(OST)中,携带 P/LP 变异的患者 GH 水平降低幅度较小[17.7%(0,65.0%)vs. 80.5%(63.9%,90.2%),P=0.001],且在使用长效生长抑素类似物(SSAs)治疗 3 个月后,GH 下降幅度呈降低趋势。

结论

在中国汉族散发型肢端肥大症和垂体巨人症患者中存在种系 AIP 变异,这些变异更可能在年轻患者中被检测到。AIP 变异与侵袭性更强的肿瘤表型相关,并且对 SSA 治疗的反应较差。

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