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经典型半乳糖血症患儿及青少年的骨转换血清标志物

Serum markers of bone turnover in children and adolescents with classic galactosemia.

作者信息

Gajewska J, Ambroszkiewicz J, Radomyska B, Chełchowska M, Ołtarzewski M, Laskowska-Klita T, Milanowski A

机构信息

Department of Newborn Screening, Institute of Mother and Child, Warsaw, Poland.

出版信息

Adv Med Sci. 2008;53(2):214-20. doi: 10.2478/v10039-008-0026-8.

Abstract

PURPOSE

Classic galactosemia is an inherited metabolic disease resulting from galactose-1-phosphate uridyltransferase (GALT) deficiency. Dietary lactose exclusion reverses many clinical manifestations of acute phase of the disease. Unfortunately most of the patients, despite dietary treatment, develop long-term complications among them disturbances of bone mineralization resulting in decrease of bone mineral density (BMD). The aim of our study was to assess bone formation and resorption processes with bone turnover markers in children and adolescents with galactosemia.

MATERIALS AND METHODS

We studied 62 galactosemic children (mean age+/-SD 5.9+/-2.7 years) and adolescents (mean age+/-SD 15.6+/-2,4 years). The clinical diagnosis had been confirmed by the absence of GALT activity in erythrocytes. All patients were diagnosed in the neonatal period and had good dietary control. Healthy children (n=70) were the reference group. Serum osteocalcin (OC), bone alkaline phosphatase (BALP), collagen type I crosslinked C-telopeptide (CTX-I), 25(OH)D metabolite of vitamin D were determined by ELISA assays.

RESULTS

We observed similar mean values of bone formation markers in children with galactosemia as compared to the age-matched controls. The level of bone resorption marker CTX-I in these patients was lower by about 20% (p<0.001) than in healthy children. On the contrary we obtained slightly higher values of CTX-I in adolescents with galactosemia in comparison to the age-matched controls. In these patients the values of OC and BALP were significantly higher than in healthy adolescents (111.8+/-52.1 microg/L versus 82.3+/-43.0 microg/L, p<0.02; and 95.4+/-45.7 U/L versus 72.6+/-40.6 U/L, p<0.05 respectively).

CONCLUSION

Our results suggest that bone turnover in galactosemic patients elevates from childhood to adolescence, whereas in healthy individuals there is a decline during aging. Further studies on adults with galactosemia are necessary to assess bone status in these patients.

摘要

目的

经典型半乳糖血症是一种由于1-磷酸半乳糖尿苷转移酶(GALT)缺乏引起的遗传性代谢疾病。饮食中排除乳糖可逆转该疾病急性期的许多临床表现。不幸的是,大多数患者尽管接受了饮食治疗,但仍会出现长期并发症,其中包括骨矿化紊乱,导致骨密度(BMD)降低。我们研究的目的是用骨转换标志物评估半乳糖血症儿童和青少年的骨形成和吸收过程。

材料与方法

我们研究了62名半乳糖血症儿童(平均年龄±标准差5.9±2.7岁)和青少年(平均年龄±标准差15.6±2.4岁)。临床诊断通过红细胞中缺乏GALT活性得以证实。所有患者均在新生儿期被诊断出来,并且饮食控制良好。健康儿童(n = 70)作为参照组。通过酶联免疫吸附测定法测定血清骨钙素(OC)、骨碱性磷酸酶(BALP)、I型胶原交联C末端肽(CTX-I)、维生素D的25(OH)D代谢产物。

结果

与年龄匹配的对照组相比,我们观察到半乳糖血症儿童的骨形成标志物平均值相似。这些患者的骨吸收标志物CTX-I水平比健康儿童低约20%(p<0.001)。相反,与年龄匹配的对照组相比,我们发现半乳糖血症青少年的CTX-I值略高。在这些患者中,OC和BALP的值显著高于健康青少年(分别为111.8±52.1μg/L对82.3±43.0μg/L,p<0.02;以及95.4±45.7 U/L对72.6±40.6 U/L,p<0.05)。

结论

我们的结果表明,半乳糖血症患者的骨转换从儿童期到青少年期升高,而在健康个体中随着年龄增长则下降。有必要对成年半乳糖血症患者进行进一步研究,以评估这些患者的骨骼状况。

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