Bone health in phenylketonuria: a systematic review and meta-analysis

• Authors: Serwet Demirdas, University of Amsterdam; Katie E. Coakley, Emory University; Peter H. Bisschop, University of Amsterdam; Carla E. M. Hollak, University of Amsterdam; Annet M. Bosch, University of Amsterdam; Rani Singh, Emory University
• Journal Title: Orphanet Journal of Rare Diseases
• Volume: Volume 10, Number 1
• Publisher: BioMed Central | 2015-02-15, Pages 17-17
• Type of Work: Article | Final Publisher PDF
• Publisher DOI: http://doi.org/10.1186/s13023-015-0232-y
• Subjects: Health Sciences, Nutrition; Biology, Genetics
• Keywords: Science & Technology; Life Sciences & Biomedicine; Genetics & Heredity; Medicine, Research & Experimental; Research & Experimental Medicine; Phenylketonuria; PKU; Bone mineral density; BMD; Bone turnover markers; Phenylalanine; Osteopenia; Osteoporosis; Meta-analysis; Systematic review; PEDIATRIC OFFICIAL POSITIONS; MINERAL DENSITY; CHILDREN; OSTEOPOROSIS; RECOMMENDATIONS; ADOLESCENTS; GUIDELINES; CHALLENGES; PREVENTION; MANAGEMENT

Abstract

Patients with Phenylketonuria (PKU) reportedly have decreased bone mineral density (BMD). The primary aim of this study was to perform a systematic review and meta-analysis to determine the extent and significance of low BMD in early treated patients with PKU. Secondary aims were to assess other bone status indicators including bone turnover markers (BTM) and to define areas for future research. Two research teams (Amsterdam, Netherlands and Atlanta, USA) performed literature searches for articles reporting data on BMD, osteopenia and osteoporosis, BTM or other bone indicators in patients with PKU. Included articles were compared between research teams and assessed for quality and risk of bias. A total of 13 unique articles were included; 11/13 articles reported BMD including a total of 360 patients. Ten out of 11 articles found BMD was significantly lower in patients with PKU. Meta-analyses for total BMD (TBMD; 3 studies; n = 133), lumbar spine BMD (LBMD; 7 studies; n = 247), and femoral neck BMD (FBMD; 2 studies; n = 78) Z-scores were performed. Overall effect sizes were: TBMD-0.45 (95% CI-0.61,-0.28); LBMD-0.70 (95% CI-0.82,-0.57); FBMD-0.96 (95% CI-1.42,-0.49). Definitions of osteopenia and osteoporosis were highly heterogeneous between studies and did not align with World Health Organization standards and the International Society for Clinical Densitometry positions on BMD measurement. Despite individual study findings of low BMD indicating higher risk of osteoporosis, pooled available data suggest reduction in BMD is not clinically important when using standard definitions of low BMD. Results from studies evaluating BTM are inconclusive. Phenylalanine concentration, vitamin D, PTH, and nutrient intake do not correlate with BMD or BTM. We recommend forthcoming studies use standard definitions of low BMD to determine clinical implications of BMD Z-scores below 0, explore cause of low BMD in the subset of patients with low BMD for chronological age (Z-score <-2) and assess fracture risk in patients with PKU.