Kuppens R J, Mahabier E F, Bakker N E, Siemensma E P C, Donze S H, Hokken-Koelega A C S
Dutch Growth Research Foundation, Rotterdam, The Netherlands.
Department of Pediatrics, Erasmus University Medical Center-Sophia Children's Hospital, Subdivision of Endocrinology, Westzeedijk 106, 3016 AH, Rotterdam, The Netherlands.
Orphanet J Rare Dis. 2016 Nov 16;11(1):153. doi: 10.1186/s13023-016-0535-7.
Patients with Prader-Willi syndrome (PWS) have a cognitive impairment. Growth hormone (GH) treatment during childhood improves cognitive functioning, while cognition deteriorates in GH-untreated children with PWS. Cessation of GH treatment at attainment of adult height (AH) might deteriorate their GH-induced improved cognition, while continuation might benefit them. We, therefore, investigated the effects of placebo versus GH administration on cognition in young adults with PWS who were GH-treated for many years during childhood and had attained AH.
Two-year, randomized, double-blind, placebo-controlled cross-over study in 25 young adults with PWS. Cross-over intervention with placebo and GH (0.67 mg/m/day), both during 1 year.
Total (TIQ), verbal (VIQ) and performance IQ (PIQ) did not deteriorate during 1 year of placebo, compared to GH treatment (p > 0.322). Young adults with a lower TIQ had significantly more loss of TIQ points during placebo versus GH, in particular VIQ decreased more in those with a lower VIQ. The effect of placebo versus GH on TIQ, VIQ and PIQ was not different for gender or genotype.
Compared to GH treatment, 1 year of placebo did not deteriorate cognitive functioning of GH-treated young adults with PWS who have attained AH. However, patients with a lower cognitive functioning had more loss in IQ points during placebo versus GH treatment. The reassuring finding that 1 year of placebo does not deteriorate cognitive functioning does, however, not exclude a gradual deterioration of cognitive functioning on the long term.
ISRCTN24648386 , NTR1038 , Dutch Trial Register, www.trialregister.nl . Registered 16 August 2007.
普拉德-威利综合征(PWS)患者存在认知障碍。儿童期生长激素(GH)治疗可改善认知功能,而未经GH治疗的PWS儿童认知功能会恶化。成年身高(AH)达成后停止GH治疗可能会使GH诱导改善的认知功能恶化,而继续治疗可能对他们有益。因此,我们研究了安慰剂与GH给药对童年期接受多年GH治疗且已达成AH的PWS青年认知的影响。
对25名PWS青年进行为期两年的随机、双盲、安慰剂对照交叉研究。交叉干预,安慰剂和GH(0.67mg/m/天)各治疗1年。
与GH治疗相比,安慰剂治疗1年期间,总智商(TIQ)、言语智商(VIQ)和操作智商(PIQ)均未恶化(p>0.322)。TIQ较低的青年在接受安慰剂治疗期间TIQ得分的损失明显多于接受GH治疗,尤其是VIQ较低者的VIQ下降更多。安慰剂与GH对TIQ、VIQ和PIQ的影响在性别或基因型方面无差异。
与GH治疗相比,1年的安慰剂治疗并未使已达成AH的接受过GH治疗的PWS青年的认知功能恶化。然而,认知功能较低的患者在接受安慰剂治疗期间比接受GH治疗时智商得分损失更多。不过,令人放心的是,1年的安慰剂治疗并未使认知功能恶化,但这并不排除长期认知功能会逐渐恶化。
ISRCTN24648386,NTR1038,荷兰试验注册中心(www.trialregister.nl)。2007年8月16日注册。