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Health-related quality of life of young adults with Turner syndrome following a long-term randomized controlled trial of recombinant human growth hormone

机译:重组人生长激素的长期随机对照试验后,特纳综合征的年轻成年人的健康相关生活质量

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Background There are limited long-term randomized controlled trials of growth hormone (GH) supplementation to adult height and few published reports of the health-related quality of life (HRQOL) following treatment. The present follow-up study of young adults from a long-term controlled trial of GH treatment in patients with Turner syndrome (TS) yielded data to examine whether GH supplementation resulted in a higher HRQOL (either due to taller stature or from the knowledge that active treatment and not placebo had been received) or alternatively a lower HRQOL (due to medicalization from years of injections). Methods The original trial randomized 154 Canadian girls with TS aged 7-13 years from 13 centres to receive either long-term GH injections at the pharmacologic dose of 0.3 mg/kg/week or to receive no injections; estrogen prescription for induction of puberty was standardized. Patients were eligible for the follow-up study if they were at least 16 years old at the time of follow-up. The instrument used to study HRQOL was the SF-36, summarized into physical and mental component scales (PCS and MCS); higher scores indicate better HRQOL. Results Thirty-four of the 48 eligible participants (71%) consented to participate; data were missing for one patient. Both groups (GH and no treatment) had normal HRQOL at this post-treatment assessment. The GH group had a (mean ± SD) PCS score of 56 ± 5; the untreated group 58 ± 4; mean score for 16-24 year old females in the general population 53.5 ± 6.9. The GH group had a mean MCS score of 52 ± 6; the untreated group 49 ± 13; mean score for 16-24 year old females in the general population 49.6 ± 9.8. Secondary analyses showed no relationship between HRQOL and height. Conclusions We found no benefit or adverse effect on HRQOL either from receiving or not receiving growth hormone injections in a long-term randomized controlled trial, confirming larger observational studies. We suggest that it remains ethically acceptable as well as necessary to maintain a long-term untreated control group to estimate the effects of pharmacological agents to manipulate adult height. Young adult women with TS have normal HRQOL suggesting that they adjust well to their challenges in life. Trial Registration ClinicalTrials.gov Identifier NCT00191113 .
机译:背景技术仅有有限的长期生长激素(GH)补充成人身高的随机对照试验,并且很少有关于治疗后健康相关生活质量(HRQOL)的公开报道。这项针对特纳综合症(TS)患者的GH治疗的长期对照试验对年轻人进行的最新追踪研究得出的数据可以检查GH补充剂是否导致较高的HRQOL(由于身材较高或以下原因导致:积极治疗但未接受安慰剂)或较低的HRQOL(由于多年的注射使患者医疗化)。方法最初的试验从13个中心对154名7-13岁TS的加拿大女孩进行了随机分组,他们以0.3 mg / kg /周的药理剂量长期接受GH注射或不注射。诱导青春期的雌激素处方已标准化。如果患者在随访时年满16岁,则符合随访研究的条件。用于研究HRQOL的工具是SF-36,概括为身体和精神成分量表(PCS和MCS);分数越高表明HRQOL越好。结果48名合格参与者中有34名(71%)同意参加。一名患者的数据丢失。在此治疗后评估中,两组(GH和未治疗)的HRQOL均正常。 GH组的PCS评分为(平均±SD)56±5。未经治疗的组58±4;普通人群中16-24岁女性的平均得分为53.5±6.9。 GH组的平均MCS评分为52±6;未经治疗的组为49±13;普通人群中16-24岁女性的平均得分为49.6±9.8。次要分析显示HRQOL与身高之间没有关系。结论在一项长期的随机对照试验中,我们发现注射或不注射生长激素对HRQOL均无益处或不利影响,从而证实了较大的观察性研究。我们建议在伦理上仍然可以接受,并且有必要保持长期未治疗的对照组以评估药理剂对成人身高的影响。患有TS的年轻成年女性的HRQOL正常,表明他们可以很好地适应生活中的挑战。试用注册ClinicalTrials.gov标识符NCT00191113。

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