Natural History of Perinatal and Infantile Hypophosphatasia: A Retrospective Study

J Pediatr. 2019 Jun:209:116-124.e4. doi: 10.1016/j.jpeds.2019.01.049. Epub 2019 Apr 9.

Abstract

Objective: To report clinical characteristics and medical history data obtained retrospectively for a large cohort of pediatric patients with perinatal and infantile hypophosphatasia.

Study design: Medical records from academic medical centers known to diagnose and/or treat hypophosphatasia were reviewed. Patients born between 1970 and 2011 with hypophosphatasia and any of the following signs/symptoms at age <6 months were eligible: vitamin B6-dependent seizures, respiratory compromise, or rachitic chest deformity (NCT01419028). Patient demographics and characteristics, respiratory support requirements, invasive ventilator-free survival, and further complications of hypophosphatasia were followed for up to the first 5 years of life.

Results: Forty-eight patients represented 12 study sites in 7 countries; 13 patients were alive, and 35 were dead (including 1 stillborn). Chest deformity, respiratory distress, respiratory failure (as conditioned by the eligibility criteria), failure to thrive, and elevated calcium levels were present in >70% of patients between birth and age 5 years. Vitamin B6-dependent seizures and respiratory distress and failure were associated significantly (P < .05) with the risk of early death. Serum alkaline phosphatase activity in all 41 patients tested (mean [SD]: 18.1 [15.4] U/L) was below the mean lower limit of normal of the reference ranges of the various laboratories (88.2 U/L). Among the 45 patients with relevant data, 29 had received respiratory support, of whom 26 had died at the time of data collection. The likelihood of invasive ventilator-free survival for this cohort decreased to 63% at 3 months, 54% at 6 months, 31% at 12 months, and 25% at 5 years.

Conclusions: Patients with perinatal or infantile hypophosphatasia and vitamin B6-dependent seizures, with or without significant respiratory distress or chest deformities, have high morbidity and mortality in the first 5 years of life.

Trial registration: ClinicalTrials.gov: NCT01419028.

Keywords: alkaline phosphatase; craniosynostosis; invasive ventilation; metabolic bone disease; rickets; survival.

Publication types

  • Multicenter Study

MeSH terms

  • Alkaline Phosphatase / blood*
  • Alkaline Phosphatase / therapeutic use
  • Cause of Death*
  • Cohort Studies
  • Disease Progression
  • Disease-Free Survival
  • Enzyme Replacement Therapy / methods*
  • Enzyme Replacement Therapy / mortality
  • Female
  • Follow-Up Studies
  • Humans
  • Hypophosphatasia / blood
  • Hypophosphatasia / diagnosis
  • Hypophosphatasia / mortality*
  • Hypophosphatasia / therapy*
  • Infant
  • Internationality
  • Kaplan-Meier Estimate
  • Male
  • Pregnancy
  • Retrospective Studies
  • Risk Assessment
  • Severity of Illness Index
  • Survival Analysis
  • Time Factors

Substances

  • Alkaline Phosphatase

Supplementary concepts

  • Hypophosphatasia, Infantile