25 Hydroxy Vitamin D Level, Bone Health, Vitamin D and Calcium Intake in Chilean Patients with Phenylketonuria and Hyperphenylalaninemias

Q3 Medicine
C. Leiva, P. Bravo, C. Arias, J. Cabello, M. J. Leal-Witt, F. Salazar, V. Cornejo
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引用次数: 1

Abstract

Abstract It has been shown that there is a decrease in the concentrations of 25 hydroxyvitamin D (25-OHD) and bone mineral density (BMD) in patients with phenylketonuria (PKU) in their follow-up. Our objective was to determine concentrations of 25-OHD in subjects with PKU and hyperphenylalaninemia (HPA). Transversal analytical study considered three groups: G1-PKU with neonatal diagnosis and formula intake without Phe; G2-HPA, without specific treatment and G3-C control group. Sixteen patients per group (aged 6-23) were included. Levels of 25-OHD, lumbar spine (L2-L4), femur and total BMD, intact parathormone (PTH) and vitamin D (VitD) and calcium intake were calculated. The Kruskal-Wallis statistical test was applied (p-value 30 ng/mL). G1-PKU had a higher intake of VitD, with differences among groups. There were no significant differences among groups in relation to BMD and intact PTH. In conclusion, G1-PKU under treatment and with good adherence, does not present VitD deficiency and no BMD alterations are observed. In contrast, G2-HPA had a lower intake of VitD and decreased 25-OHD concentrations which could affect the bone architecture in the long term. Further studies on the G2-HPA are suggested.
智利苯丙酮尿和高苯丙氨酸血症患者羟基维生素D水平、骨骼健康、维生素D和钙摄入量
摘要:有研究表明,苯丙酮尿症(PKU)患者的25羟基维生素D (25- ohd)浓度和骨密度(BMD)在随访中有所下降。我们的目的是测定PKU和高苯丙氨酸血症(HPA)患者体内25-OHD的浓度。横向分析研究考虑了三组:G1-PKU新生儿诊断和配方奶粉摄入没有Phe;G2-HPA组,无特异性治疗组和G3-C对照组。每组16例患者(6-23岁)。计算25-OHD水平、腰椎(L2-L4)、股骨和总骨密度、完整甲状旁腺激素(PTH)、维生素D (VitD)和钙摄入量。采用Kruskal-Wallis统计检验(p值30 ng/mL)。G1-PKU组维生素d摄取量较高,但组间存在差异。各组间骨密度和完整甲状旁腺功能无显著差异。总之,G1-PKU在治疗和良好的依从性下,没有出现维生素d缺乏,也没有观察到BMD改变。相比之下,G2-HPA的维生素d摄入量较低,25-OHD浓度降低,长期影响骨结构。建议进一步研究G2-HPA。
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来源期刊
CiteScore
0.60
自引率
0.00%
发文量
7
审稿时长
12 weeks
期刊介绍: The Journal of Inborn Errors of Metabolism and Screening (JIEMS) is an online peer-reviewed open access journal devoted to publishing clinical and experimental research in inherited metabolic disorders and screening, for health professionals and scientists. Original research articles published in JIEMS range from basic findings that have implications for disease pathogenesis and therapy, passing through diagnosis and screening of metabolic diseases and genetic conditions, and therapy development and outcomes as well. Original articles, reviews on specific topics, brief communications and case reports are welcome. JIEMS aims to become a key resource for geneticists, genetic counselors, biochemists, molecular biologists, reproductive medicine researchers, obstetricians/gynecologists, neonatologists, pediatricians, pathologists and other health professionals interested in inborn errors of metabolism and screening.
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