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加拿大肢端肥大症诊断和治疗的新趋势。

Emerging trends in the diagnosis and treatment of acromegaly in Canada.

机构信息

CHUM, University of Montreal, Montreal, QC, Canada.

出版信息

Clin Endocrinol (Oxf). 2013 Jul;79(1):79-85. doi: 10.1111/cen.12112. Epub 2013 Apr 27.

DOI:10.1111/cen.12112
PMID:23190441
Abstract

OBJECTIVE

To evaluate demographic data and quality of care of patients with acromegaly in Canada and their evolution over time and secondly, to evaluate predictors of co-morbidities and treatment outcomes.

DESIGN AND PATIENTS

Retrospective analyses of clinical, biochemical and treatment outcome data of 649 patients with acromegaly (males: 50·7%) followed from 1980 to 2010 (mean 10·2 years, SD 13·7) in eight tertiary care centres from six Canadian provinces.

RESULTS

In comparison to 1980-1994, the number of patients referred with acromegaly in the last 15 years was higher with female preponderance (52·8% vs 41·4%, P = 0·01) and an older age at diagnosis (46·4 ± 14 vs 41·3 ± 12 years, P < 0·0001). Diabetes was present in 28%, hypertension in 37% and sleep apnoea in 33% of cases. Pretreatment IGF-1 levels, but not GH levels were significant predictors of diabetes (P = 0·0002) and hypertension (P < 0·0001). Eighty-nine per cent of patients underwent pituitary surgery, 64·5% had medical therapy and 22% received radiotherapy. Radiotherapy was less utilized in the past 15 years (16% vs 45%, P < 0·0001). Multimodal therapy achieved remission or control of acromegaly in 70% of patients. Patients in remission or disease control had lower initial random GH (P = 0·04) and IGF-1 levels (P < 0·0001). Hypopituitarism was present in 23% of patients and cancer in 8·5%.

CONCLUSIONS

There was an increase over time of referral for acromegaly management with female predilection. Initial higher IGF-1, but not GH levels, were predictive of co-morbidities and persistent active disease after treatment. Disease remission or control was attained in 70% of patients utilizing multimodal therapy.

摘要

目的

评估加拿大肢端肥大症患者的人口统计学数据和治疗质量,并评估其随时间的变化情况,其次评估合并症和治疗结果的预测因素。

设计和患者

对来自加拿大六个省份的八个三级保健中心的 649 例肢端肥大症患者(男性:50.7%)的临床、生化和治疗结果数据进行回顾性分析,这些患者从 1980 年至 2010 年(平均随访 10.2 年,标准差 13.7 年)。

结果

与 1980-1994 年相比,过去 15 年中因肢端肥大症就诊的患者数量更多,女性比例更高(52.8%对 41.4%,P=0.01),诊断时年龄更大(46.4±14 岁对 41.3±12 岁,P<0.0001)。28%的患者有糖尿病,37%的患者有高血压,33%的患者有睡眠呼吸暂停。治疗前 IGF-1 水平,但不是 GH 水平是糖尿病(P=0.0002)和高血压(P<0.0001)的显著预测因素。89%的患者接受了垂体手术,64.5%的患者接受了药物治疗,22%的患者接受了放疗。过去 15 年中放疗的使用率较低(16%对 45%,P<0.0001)。多模式治疗使 70%的患者达到缓解或控制肢端肥大症。缓解或疾病控制的患者初始随机 GH(P=0.04)和 IGF-1 水平较低(P<0.0001)。23%的患者有垂体功能减退,8.5%的患者有癌症。

结论

随着时间的推移,肢端肥大症的治疗转诊率呈上升趋势,女性更倾向于接受治疗。初始较高的 IGF-1,但不是 GH 水平,可预测合并症和治疗后持续的活动性疾病。70%的患者通过多模式治疗达到缓解或控制。

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