Keywords
alkaline phosphatase - children - parathyroid hormone - radius fractures - vitamin
D
Introduction
Distal radius fractures are one of the most common types of fractures, with an incidence
of 25% in the pediatric population.[1] With puberty, the incidence of these fractures rises, with a peak in the age group
between 8 and 11 years in girls, and between 11 and 14 years in boys.[2] Although the exact cause has not yet been discovered, the incidence has demonstrated
a steady increase over the past 40 years.[2]
[3] Several studies have been conducted to find out the source of the increased rates,
trying to carefully elucidate the potential factors. A general increase in the participation
in sports-related activities, gender, ethnic and racial differences, and nutritional
status are some of the factors which have been investigated in the literature related
with the occurrence of distal radius fractures in the pediatric population.[4]
[5]
The positive effects of vitamin D on bone density and the association between vitamin
D deficiency and low bone density have been established with several studies.[4]
[5]
[6] Low dietary intake of minerals, such as calcium, magnesium, and phosphate, also
causes decreased bone mineral density and increased risk of osteoporotic fracture.[7]
[8]
[9] Primary or secondary osteoporosis caused by various underlying chronic illnesses
may lead to low serum levels of minerals and vitamin D in the pediatric population,
as well as to an increase in the risk of pediatric fracture.[10]
[11] Although there is a consensus in the literature about the direct correlation between
low dietary mineral intake or low levels of vitamin D and osteoporotic fractures in
adults, there is no adequate data to find any correlation between the serum levels
of vitamin D and minerals and isolated distal radius fractures in children. Therefore,
we aimed to compare the serum levels of vitamin D and minerals in children with and
without isolated distal radius fractures.
Materials and Methods
The present prospective clinical study was performed with the approval of the Insitutional
Review Board (approval number: 19/12/2017-2427) and in line with the ethical principles
of the Declaration of Helsinki. After the approval, informed consent was obtained
from the guardians of all participants.
The inclusion criteria were: children aged between 5 and 15 years, with similar socioeconomic
background, no history of malnutrition or undernutrition, those needing to examine
the bone mineral density, with adequate sunlight exposure, otherwise healthy apart
from the distal radius fracture after mild trauma, with no history of upper-extremity
surgery, and no neurological diseases. The exclusion criteria were: children with
concurrent ulnar fractures, history of major trauma, with mineralization disorders
(osteopenia, osteogenesis imperfecta, etc.), undergoing steroid treatment, and with
chronic diseases or cerebral palsy.
In total, 50 children who were admitted to our emergency unit between February and
May 2018 with isolated distal radius fractures ([Fig. 1]) were included in the study group (group A), and 50 healthy children with no history
of fracture were included as the control group (group B). The patients in group B
were randomly recruited from pediatric outpatient units; they had upper respiratory
tract infection or were being submitted to routine examinations.
Fig. 1 Anteroposterior and lateral radiograps of an isolated distal radius fracture.
The following characteristics of the study sample were included: age (years), gender
distribution, height (cm), weight (kg), and body mass index (BMI; kg/m2). Peripheral venous blood samples were obtained and analyzed for measurements of
25-hydroxyvitamin D (25(OH)D), calcium (Ca), magnesium (Mg), phosphorus (P), alkaline
phosphatase (ALP), and parathyroid hormone (PTH).
Statistical Analysis
The Statistical Package for the Social Sciences (SPSS, IBM Corp., Armonk, NY, US)
software, version 22.0 for Windows 7, was used for all statistical analyses. The data
was presented as means and standard deviations, medians, minimum and maximum ranges,
frequencies and rates. The distributions of the parametric data were analyzed with
the aid of the Student t-test, and the Mann-Whitney U test was used for the non-parametric data. The Chi-squared
test was employed to compare the rates between the two groups. Values of p < 0.05 were considered statistically significant.
Results
The sample was composed of 100 patients, with 50 patients in the control group and
50 in the study group. All patients in the study group had isolated distal radius
fractures, and those in the control group had no history of fracture.
The mean age, height, weight, BMI and gender distribution were similar in both groups
([Table 1]). In addition, there were no obese patients (BMI > 30) in the sample. There were
no statistical differences in the blood analyses, including Ca, Mg, P, ALP, and PTH
([Table 2]). However, the serum levels of 25(OH)D were statistically lower in the group A when
compared to group B (p < 0.001), and the number of patients with 25(OH)D insufficiency was statistically
higher in group A than in group B (p = 0.012).
Table 1
|
Group A (n = 50)
|
Group B (n = 50)
|
p-value
|
|
Age (years)
|
8.3 ± 2.8 (5–15)
|
7.9 ± 3.4 (5–15)
|
0.352
|
|
Gender (female); n (%)
|
18 (36.0)
|
16 (32.0)
|
0.765
|
|
Height (cm)
|
118.8 ± 22.3 (90–165)
|
116.4 ± 24.9 (76–160)
|
0.716
|
|
Weight (kg)
|
29.8 ± 9.8 (15–56)
|
27.8 ± 11.9 (13–55)
|
0.268
|
|
Body mass index (kg/m2)
|
21.4 ± 4.9 (13.6–29.6)
|
20.5 ± 3.2 (12.2–28.1)
|
0.412
|
Table 2
|
Group A (n = 50)
|
Group B (n = 50)
|
p-value
|
|
Calcium (mg/dL)
|
10.0 ± 0.4 (9.4–10.7)
|
10.1 ± 0.6 (9.1–11.4)
|
0.542
|
|
Magnesium (mg/dL)
|
2.11 ± 0.14 (1.8–2.4)
|
2.10 ± 0.15 (1.9–2.4)
|
0.830
|
|
Phosphorus (mg/dL)
|
5.0 ± 0.40 (4.3–5.8)
|
5.12 ± 0.48 (4–6.3)
|
0.350
|
|
Alkaline phosphatase (IU/L)
|
276.4 ± 69.4 (200–482)
|
286.6 ± 72.6 (167–447)
|
0.478
|
|
Parathyroid hormone (pg/mL)
|
41.7 ± 22.3 (10.9–97.1)
|
40.1 ± 19.1 (18.6–77.2)
|
0.676
|
|
25-hydroxyvitamin D (ng/mL)
|
19.4 ± 4.2 (10.7–28.3)
|
29.4 ± 11.1 (13–48.7)
|
< 0.001
|
|
25-hydroxyvitamin D insufficiency; n (%)
|
22 (44.0)
|
6 (12.0)
|
0.012
|
Discussion
Fractures compose around 10% to 25% of all pediatric injuries, and one of the most
common in the pediatric population is distal radius fracture.[12]
[13] Approximately 1 in 100 children are hospitalized for orthopedic surgery after distal
radius fractures yearly. The wide spectrum of fracture presentation, the variety of
surgical and non-surgical techniques, the growth potential of the skeletal structure
of the children, and family expectations are some of the challenging factors in the
treatment of distal radius fractures, especially in the pediatric population.[14] Due to accelerated skeletal maturation, children and adolescents are at a high risk
for these fractures. Ryan et al.[15] revealed a significant higher rate of fractures caused by minor trauma in the age
group between10 and 14 years in comparison with the age group between 5 and 9 years.
This finding implies that rapid skeletal development may jeopardize bone mineralization,
which is disproportional to the growth rate, and may lead to a distal radius fracture
even after a minor trauma.
Solar ultraviolet B (UV-B) radiation is the primary source of vitamin D (other than
dietary intake). Vitamin D3, which is produced by the skin with the action of sunlight,
and dietary vitamin D undergo two consecutive hydroxylations: in the liver, the former
becomes 25(OH)D, and, in the kidneys, the latter takes on its biologically-active
form, 1,25-dihydroxyvitamin D (1,25(OH)2D); 1,25(OH)2D enhances the serum levels of
calcium and phosphorus by increasing the intestinal absorption of these minerals,
which are involved in the processes of bone formation, mineralization, and resorption.[16] Serum 25(OH)D is a major circulating metabolite of vitamin D, and it clinically
reflects the status of this vitamin, which may be used as an indicator of the lifestyle
and dietary habits of the patients. The serum concentrations of 25(OH)D that indicate
deficiency or insufficiency of vitamin D are controversial, and the cut-off values
are not well–established. The American Academy of Pediatrics (AAP) and the Institute
of Medicine (IOM) both define vitamin D insufficiency as concentrations of 25(OH)D < 20 ng/mL
in the pediatric population.[10] We used the Endocrine Society guideline, which defines the deficiency of 25(OH)D
as levels < 20 ng/mL, and the insufficiency as levels < 30 ng/mL.[17]
Vitamin D deficiency affects the intestinal absorption of calcium and phosphorus,
which results in decreased serum levels of those minerals. The parathyroid gland releases
hormone to increase the serum calcium back into the adequate range. The PTH increases
the calcium reabsorption in the kidneys and the excretion of phosphorus. Meanwhile,
it has also negative effects on bone mineralization, with the aim of increasing the
serum levels of calcium.
Over time, chronic severe vitamin D deficiency in infants and children causes stunted
growth, osteomalacia, and rickets.[10] Moore et al.[18] reported that vitamin D deficiency has a higher incidence among obese children and
those with darker skin. Similarly, vitamin D deficiency was found to be more frequent
in girls than in boys.
Vitamin D, PTH and calcium levels have been correlated with bone mineral density.[19] The association between 25(OH)D and bone mineral density has been examined in several
studies.[20]
[21]
[22]
[23] Most of these studies showed a connection between the adequate intake of vitamin
D and high bone mineral density. Low bone mineral density may increase the rate of
fracture both in the adult and pediatric populations.[23]
[24]
[25] A study[21] that assessed the status of vitamin D in adolescent girls during winter found that
low levels of vitamin D have a negative effect on bone mineral density. Another study,[24] which analyzed calcium supplementation and bone mineral density, showed a positive
effect of vitamin D supplementation on high bone mineral density, which may reduce
the rate of pediatric fracture. In the present study, we found that children with
distal radius fracture have statistically lower levels of vitamin D than the healthy
group. On the other hand, between the two groups there were no statistically significant
differences regarding the levels of Ca, Mg, P, ALP, and PTH.
Adolescents are prone to vitamin D insufficiency due to the mineral demands of their
growing skeleton. A study[25] conducted in northern India found a high prevalence of clinical and biochemical
hypovitaminosis D in healthy schoolchildren. Vitamin D deficiency in healthy children
has been subjected to several studies,[26]
[27]
[28]
[29] which showed that sunlight exposure alone is not enough to prevent hypovitaminosis
D, and that nutritional habits (high dietary phytate intake) or genetic tendency (Asian)
may lead to vitamin D deficiency. In the present study, we observed that 12% of the
healthy children had vitamin D levels < 20 ng/mL, which are considered deficient.
One of the limitations of the present study is that the blood samples were collected
from the children regardless of the season; thus, some children may not have had enough
time to produce vitamin D, especially at the end of winter. Another limitation of
the study is the lack of information about the dietary habits of the children in the
sample. More detailed studies with larger samples are needed in order to find more
convincing data about the correlation of vitamin D and pediatric fractures.
Conclusion
Although optimal vitamin D levels have not been well-established in the literature,
they have been used to determine bone health.[29] Besides vitamin D levels, minerals such as Ca, Mg and P or endocrine hormones (PTH)
have also been used as determinants of bone turnover. In adults, an association between
hypovitaminosis D and osteoporotic fractures has been examined in several studies.[26]
[28] However, in the pediatric population, there is no adequate study to determine any
correlation between pediatric fractures and vitamin D deficiency. With the present
study, we have shown that the status of vitamin D may be used as a predictor of pediatric
fractures. Especially in spring and summer, families with children with isolated distal
radius fractures should be informed about vitamin D deficiency, and, in children with
low levels of vitamin D, supplementation may be considered.
