Graduate Program in Medical Sciences Medicine, Department of Medical College, Universidade Federal do Rio Grande do Sul, Porto Alegre 90040-060, Brazil.
Graduate Program in Genetics and Molecular Biology, Department of Genetics, Universidade Federal do Rio Grande do Sul, Porto Alegre 90040-060, Brazil.
Nutrients. 2021 Aug 27;13(9):2987. doi: 10.3390/nu13092987.
The association between bone mineral density (BMD) and hepatic glycogen storage diseases (GSDs) is still unclear. To evaluate the BMD of patients with GSD I, IIIa and IXα, a cross-sectional study was performed, including 23 patients (GSD Ia = 13, Ib = 5, IIIa = 2 and IXα = 3; median age = 11.9 years; IQ = 10.9-20.1) who underwent a dual-energy X-ray absorptiometry (DXA). Osteocalcin (OC, = 18), procollagen type 1 N-terminal propeptide (P1NP, = 19), collagen type 1 C-terminal telopeptide (CTX, = 18) and 25-OH Vitamin D ( = 23) were also measured. The participants completed a 3-day food diary ( = 20). Low BMD was defined as a Z-score ≤ -2.0. All participants were receiving uncooked cornstarch (median dosage = 6.3 g/kg/day) at inclusion, and 11 (47.8%) presented good metabolic control. Three (13%) patients (GSD Ia = 1, with poor metabolic control; IIIa = 2, both with high CPK levels) had a BMD ≤ -2.0. CTX, OC and P1NP correlated negatively with body weight and age. 25-OH Vitamin D concentration was decreased in seven (30.4%) patients. Our data suggest that patients with hepatic GSDs may have low BMD, especially in the presence of muscular involvement and poor metabolic control. Systematic nutritional monitoring of these patients is essential.
骨密度(BMD)与肝糖原贮积病(GSD)之间的关系尚不清楚。为了评估 GSD I、IIIa 和 IXα 患者的 BMD,进行了一项横断面研究,纳入了 23 名患者(GSD Ia = 13、Ib = 5、IIIa = 2 和 IXα = 3;中位年龄 = 11.9 岁;智商 = 10.9-20.1),并对他们进行了双能 X 线吸收法(DXA)检查。还测量了骨钙素(OC, = 18)、I 型前胶原 N 端前肽(P1NP, = 19)、I 型胶原 C 端肽(CTX, = 18)和 25-羟维生素 D( = 23)。参与者完成了 3 天的饮食日记( = 20)。低 BMD 定义为 Z 评分≤-2.0。所有患者在纳入时均接受生玉米淀粉治疗(中位数剂量 = 6.3 g/kg/天),11 名(47.8%)患者代谢控制良好。3 名(13%)患者(GSD Ia = 1,代谢控制不佳;IIIa = 2,均伴有高肌酸激酶水平)BMD ≤-2.0。CTX、OC 和 P1NP 与体重和年龄呈负相关。7 名(30.4%)患者的 25-羟维生素 D 浓度降低。我们的数据表明,肝 GSD 患者可能存在低 BMD,尤其是在存在肌肉受累和代谢控制不佳的情况下。对这些患者进行系统的营养监测至关重要。