Author/Authors :
Shakiba, Marjan Department of Pediatric Endocrinology and Metabolic diseases - Mofid children hospital - Shahid Beheshti University of Medical Sciences, Tehran , Alaei, Mohammad reza Department of Pediatric Endocrinology and Metabolic diseases - Mofid children hospital - Shahid Beheshti University of Medical Sciences, Tehran , Saneifard, Hedyeh Department of Pediatric Endocrinology and Metabolic diseases - Mofid children hospital - Shahid Beheshti University of Medical Sciences, Tehran , Mosallanejad, Asieh Department of Pediatric Endocrinology and Metabolic diseases - Mofid children hospital - Shahid Beheshti University of Medical Sciences, Tehran
Abstract :
Dietary phenylalanine restriction is the main treatment of
phenylketonuria (PKU, OMIM 261600). There are a number of studies
which have demonstrated growth retardation in these patients, and
some are in contrast. This study was performed to assess the growth
parameters of treated PKU patients.
Materials & Methods
This cross-sectional study was performed between 2015 and 2017 to
compare growth indexes in PKU patients in our clinics with normal
age and sex matched controls. Weight, height, head circumference
(HC), weight for height and BMI (weight/height2) were measured and
converted into Z-scores. We assessed differences between patients and
controls’ anthropometric indices in all patients and separately in patients
who were diagnosed by newborn screening program and patients
who were diagnosed after presentation of clinical manifestations in
comparison with age and sex-matched controls. Also, this difference
was assessed separately in patients aged two years and less. Correlations
between pretreatment plasma phenylalanine concentrations mean
plasma phenylalanine concentrations and anthropometric parameters
were analyzed in the patients.
Results
Overall, 209 under-treatment PKU patients (103 males, 106 females;
mean age 9.29 ± 8.7 years) and 216 controls (109 males and 107
females; mean age 8.98 ± 8.62 years) matched in terms of age, sex
and birth weight were enrolled in this study. In general, 130 patients
were diagnosed by newborn screening and 79 were diagnosed when they became symptomatic before the screening program. A significant
difference (p=0.000) was found only in HC z-score and weight for
height z-score in comparison with the control group, when we assessed
all patients. We did not find any significant differences in any of the
anthropometric indices between cases and controls who were aged 2
years old and less. Head circumference SDS and weight for height
SDS were significantly different when patients and controls who were
more than 2 years old were compared. Mean HC was significantly
lower in patients, while BMI SDS, weight SDS, and weight for height
SDS were significantly higher in PKU patients in comparison with
the control group when patients who were diagnosed in newborn
screening were assessed. Head circumference SDS, BMI, height SDS
and difference between patients’ height SDS and mid parental height
SDS had significantly lower mean scores in comparison with those of
the control group, while mean weight SDS was significantly higher
compared to controls when patients who were diagnosed after clinical
presentation were assessed.
Mean phenylalanine was not correlated with anthropometric indices,
while there was a correlation between pretreatment phenylalanine and
HC.
Conclusion
Disparities in anthropometric indexes changes observed in different
studies may be due to diverse diet protocols, availability of various
specific products and micronutrient substitutes.
Keywords :
Phenylketonuria , Growth Parameters , phenylalanine Level , Dietary restriction