Kalina Maria A, Kalina-Faska Barbara, Gruszczyńska Katarzyna, Baron Jan, Małecka-Tendera Ewa
Department of Paediatrics, Paediatric Endocrinology and Diabetes, Medical University of Silesia, Upper Silesia Centre for Child's Health ul. Medyków 16, 40-752 Katowice, Poland.
Childs Nerv Syst. 2012 Jan;28(1):121-7. doi: 10.1007/s00381-011-1594-7. Epub 2011 Sep 21.
The purpose of this study is to assess the relationship between magnetic resonance images (MRI) of the hypothalamic-pituitary (H-P) region and response to recombinant human growth hormone (rhGH) treatment in short children with growth hormone deficiency, basing on changes of auxologic parameters, as well as to answer the question if MRI may serve for selecting and monitoring the rhGH responders.
The study group comprised 85 children treated with rhGH, aged 7.3-18.7 years, followed for the mean period of 3.2 years (range, 2.1-9.5 years). Auxologic parameters (height deficit hSDS, deviation from the mid-parental height hSDS-mpSDS, bone delay index bone age/chronological age ratio (BA/CA)) were assessed before, during and at the end of rhGH treatment; growth velocity was calculated before and during rhGH therapy. Parameters were correlated with the MRI of the H-P region.
Structural anomalies of the H-P region were found in 22 (25.9%) children: empty sella syndrome (ESS) in 12 (14.1%) patients, ectopic posterior pituitary (EPP) in ten (11.8%). Patients' height deficit and their deviation from parental height before rhGH therapy was significantly greater in the EPP group (median hSDS = -3.8; hSDS-mpSDS = -2.5), bone age delay was the greatest in the ESS group (median BA/CA = 0.69), after therapy - in the EPP group (median BA/CA = 0.82). Growth velocity improved in the first year of the rhGH therapy in all groups; however, the most significant acceleration was observed in the EPP group (median delta hSDS = 0.9), then stabilised and was comparable in all groups.
MRI may be helpful in predicting response to the rhGH treatment, providing midline abnormalities are taken into account.
本研究旨在基于生长学参数的变化,评估生长激素缺乏的矮小儿童下丘脑 - 垂体(H - P)区域的磁共振成像(MRI)与重组人生长激素(rhGH)治疗反应之间的关系,并回答MRI是否可用于选择和监测rhGH反应者的问题。
研究组包括85例接受rhGH治疗的儿童,年龄7.3 - 18.7岁,平均随访3.2年(范围2.1 - 9.5年)。在rhGH治疗前、治疗期间和治疗结束时评估生长学参数(身高标准差评分身高差值hSDS、与父母平均身高的身高标准差评分差值hSDS - mpSDS、骨龄延迟指数骨龄/实际年龄比值(BA/CA));计算rhGH治疗前和治疗期间的生长速度。将这些参数与H - P区域的MRI进行相关性分析。
在22例(25.9%)儿童中发现H - P区域结构异常:12例(14.1%)患者为空蝶鞍综合征(ESS),10例(11.8%)为垂体后叶异位(EPP)。EPP组患者在rhGH治疗前的身高差值及其与父母身高的差值显著更大(中位数hSDS = -3.8;hSDS - mpSDS = -2.5),ESS组骨龄延迟最大(中位数BA/CA = 0.69),治疗后 - EPP组最大(中位数BA/CA = 0.82)。所有组在rhGH治疗的第一年生长速度均有所改善;然而,EPP组观察到最显著的加速(中位数身高标准差评分变化量delta hSDS = 0.9),然后趋于稳定且在所有组中相当。
如果考虑中线异常,MRI可能有助于预测rhGH治疗的反应。