Difference of Bigonial Width Batak Tribe in Medan City According
to Age Groups in Terms of Panoramic Radiograph
Maria Sitanggang
1
, Trelia Boel
2
, Sondang Pintauli
3
1
Master of Program, Faculty of Dentistry, Universitas Sumatera Utara, Medan 20155, North Sumatra, Indonesia
2
Unit of Oral and Maxillofacial Radiology, Faculty of Dentistry, Universitas Sumatera Utara, Medan 20155, North
Sumatra, Indonesia
3
Department of Dental Public Health, Faculty of Dentistry, Universitas Sumatera Utara, Medan 20155, North Sumatra,
Indonesia
Keywords: Bigonial Width, Panoramic Radiograph.
Abstract: Changes in mandibular morphology will occur during life-long growth and development, such as the
bigonial width, which is one of the parameters of growth and development of the mandible. The changes of
bigonial width can be measured using panoramic radiograph. The objective of this research was to
determine the difference of bigonial width of Batak tribe in Medan according to age groups based on
panoramic radiograph. The type of this research is analytical research using cross-sectional study with a
total sample of 150 people divided into five age groups, according to inclusion and exclusion criteria. Group
1 (age 4-12 years), group 2 (13-24 years, group 3 (25-34 years), group 4 (35-60 years), and group 5 (> 60
years). Measurements on the digital panoramic radiograph are done by computerized. Data that obtained
was analyzed with Oneway ANOVA and LSD. The mean value from the highest to the lowest of bigonial
width, sequentially, were in group 3 (163,283 mm ± 9,947 mm), group 4 (157,580 mm ± 7,776 mm), group
5 (155,623 mm ± 12,597 mm), group 2 (147,787 mm ± 9,108 mm), group 1 (141.917 mm ± 10.992 mm).
1 INTRODUCTION
Craniofacial is a very specific part of the body,
which is easily recognizable and distinguished
between one individual to another, and can be used
to assess one's growth and development. (Bourzgui,
2012). The mandible is one of the craniofacial parts,
where many potential landmarks provide diagnostic
information about growth and development related
to age, sex, and race. (Rachmadiani, et al., 2017).
Physical assessment of one's growth can be done
one of them by radiographic measurement.
Measurement of the mandible as one of the
parameters of growth and development with
radiography can use panoramic radiography
(Durtschi, et al., 2009) but it can also be used as an
estimate of age in forensics. (Leversha et al., 2015).
Study by means of radiographic measurements on
the mandible for an estimated age apart from the
gonial angle, the height of the ramus was also
performed on the bigonial width. (Manigandan et
al., 2015) Bigonial width is the horizontal distance
between two right and left gonial points. Bigonial
width measurements were performed on panoramic
radiographs.(Al-Shamout et al., 2012)
Indonesia is an archipelagic country, with
multicultural or multi-ethnic groups with a very large
number. (Tumonggor et al., 2013) Batak nation is
one of the tribe inhabiting the province of North
Sumatra, with a sizeable population. The Batak tribe
has five sub-tribes and each major area. Batak sub-
tribe in question are: Batak Karo, Batak Simalungun,
Batak Dairi, Batak Toba, Batak Mandailing. In the
Batak tribe (sub-Ras Proto Melayu), there is a
customary group Dalihan Na Tolu, although the term
is different but the same meaning. (Manurung, 2016)
This study was conducted to determine the
differences size of mandibular bigonial width in
Batak tribe at Rumah Sakit Gigi dan Mulut Faculty
of Dentistry, Universitas Sumatera Utara according
to age group in terms of panoramic radiography. The
purpose of this study was to find out the difference
mean value of bigonial width mandibular of Batak
tribe in Medan according to age group in terms of
panoramic radiograph, which can be used and
Sitanggang, M., Boel, T. and Pintauli, S.
Difference of Bigonial Width Batak Tribe in Medan City According to Age Groups in Terms of Panoramic Radiograph.
DOI: 10.5220/0009901100002480
In Proceedings of the International Conference on Natural Resources and Sustainable Development (ICNRSD 2018), pages 261-266
ISBN: 978-989-758-543-2
Copyright
c
2022 by SCITEPRESS Science and Technology Publications, Lda. All rights reserved
261
become a guideline in the care and growth of a
person.
2 METHODS
This analytical research conducted using cross-
sectional design, carried out at Oral-Maxillo Facial
Radiology, Faculty of Dentistry, Universitas
Sumatera Utara. The population of this study was
Batak tribe with three generations above who came
to Rumah Sakit Gigi dan Mulut Faculty of
Dentistry, Universitas Sumatera Utara and live in
Medan City. The total sample size was 150 people,
divided into five age groups. Group 1 consists of 4-
12 years old, group 2 consists of 13-24 years old,
group 3 consists of 25-34 years old, group 4
consists of 35-60 years old, and group 5 consists of
>60 years old. Each age group of samples consisted
of 30 people.
Sample selection method was done by purposive
sampling method by fulfilled inclusion and
exclusion criteria. Inclusion criteria: complete teeth
(in primary dentition period consisting of 20 teeth
and in permanent dentition period consisting of 28
teeth, except for third molar) never received
orthodontic treatment, did not use dentures.
Particularly in the age at mixed tooth period, there
is no premature loss deciduous teeth and missing of
permanent teeth, and in group 5 (age> 60 years):
full edentulous. Exclusion criteria: suffered from
systemic diseases or received treatment,
experienced of jaw surgery, odontectomy, suffered
from micrognathia, pathological conditions in the
mandible, persistence of deciduous teeth,
experienced deep caries with exposure to the pulp
and crown loss, received fullcrown or space
maintainer/space regainer treatments.
After completing the questionnaire and informed
consent, a digital of the panoramic radiography was
performed on the sample using Orthopantomograph
Instrumentarium, model QC 200 D 1-4-1, 2012. The
parameters are computerized on digital panoramic
radiograph (Fig. 1). The one-way Anova and
Multiple Comparison LSD test was done to analyze
the calculated data. Ethical clearance was obtained
from the Research Ethics Committees of Faculty of
Medicine, Universitas Sumatera Utara No.
345/TGL/KEPK FK USU-RSUP HAM/2017.
3 RESULTS
The results of normality test using one-sample
Kolmogorov-Smirnov Test showed that the variables
have normal distribution with p>0.05. Table 1
showed the mean value of bigonial width in each age
group (ANOVA test, p value = 0.000 < 0.05). The
mean value of bigonial width from the highest to the
lowest, sequentially, were in group 3 (25-34 years),
group 4 (35-60 years), group 5 (>60 years), group 2
(13-24 years), and group 1 (4-12 years).
Multiple comparison test was performed after
ANOVA analysis. Table 2 showed the significant
differences (Multiple Comparison LSD Test result)
according to age groups (p< 0.05).
Figure 1: Bigonial width in panoramic radiograph (private document).
ICNRSD 2018 - International Conference on Natural Resources and Sustainable Development
262
Table 1: The mean value of the result of the measurement
of bigonial width Batak tribe.
Groups
(y
ears
)
n
Mean ± Std.
Deviation
P
1
(
4-12
y
)
30 141.917±10.992
.000
*
2
(
13-24
y
)
30 147.787±9.108
3 (25-34y) 30 163.283±9.947
4 (35-60y) 30 157.580±7.776
5 (>60y) 30 155.623±12.611
Total 150 153.238±12.597
*One-way Anova test, sig. p<0.05
Table 2: Multiple Comparison LSD Test between five age
groups in mandibular bigonial width Batak tribe in Medan
according to age groups.
(I) Group
(years)
(J) Group
(years)
P
1 (4-12y)
2 (13-24) .028
*
3 (25-34) .001
*
4
(
35-60
)
.001
*
5
(
>60
)
.001
*
2 (13-24y)
1
(
4-12
)
.028
*
3 (25-34) .001
*
4 (35-60) .001
*
5
(
>60
)
.003
*
3 (25-34y)
1
(
4-12
)
.001
*
2
(
13-24
)
.001
*
4 (35-60) .032
*
5 (>60) .004
*
4 (35-60y)
1 (4-12) .001
*
2
(
13-24
)
.001
*
3
(
25-34
)
.032
*
5
(
>60
)
.460
5 (>60y)
1 (4-12) .001
*
2 (13-24) .003
*
3
(
25-34
)
.004
*
4
(
35-60
)
.460
4 DISCUSSION
In this study the average values of bigonial width
Batak tribe of five age groups showed the mean
value from the highest to the lowest, sequentially,
were in group 3 (25-34 years), group 4 (35-60
years), group 5 (>60 years), group 2 (13-24 years),
and group 1 (4-12 years). There was a significant
difference in bigonial width from group 1 (4-12
years) to other groups, from group 2 (13-24 years) to
other groups, and group 3 (25-34 years) to other
groups, but there was not significant difference in
bigonial width from group 4 (35-60 years) to group
5 (>60 years) (Table 2). A study conducted by Al-
Shamout et al.,, showed that there was a significant
difference in the mean values of bigonial width
between the age group of 11-19 years with the age
group of 20-29 years, 30-39 years, 40-49 years, and
50- 59 years old. Bigonial width will change with
age change.[6] The results of the same study also by
Ghaffari et al., which mentions a significant
decrease in bigonial width size from the 21-30, 31-
40, to 41-50 year age groups
. (Ghaffari et al., 2013).
The remodeling process is the process by which
old bone is removed from the skeleton (resorption)
replaced with new bone (ossification/ new bone
formation). The remodeling process occurs
throughout life, by removing old bone continuously
with new protein matrix and mineralization matrix to
form new bone. (Kini et al., 2012) The time of
children and adolescents is a very important time to
maximize accumulation of bone formation, due to
the process of growth, development, and remodeling
of bone. In both men and women, it is generally
believed that bone mass increased substantially
during the first two decades to reach peak bone mass
in adolescence or young adulthood. Several studies
have shown that peak mass bone is achieved at the
early age of 20 years but other data suggest that
bone mineral still accumulates in the third decade of
life. (Baxter-Jones et al., 2011)
After birth, the mandibular body gradually
extends towards the horizontal especially behind the
foramen mentale to produce a place for the
permanent teeth. (Al-Shamout et al., 2012) During
the process of tooth eruption in the mandible, in the
process of growth and development of the mandible,
in addition to the process of remodeling, there is also
anterior and inferior displacement. The
endocondrium of the condyle has hardening, and
affects the growth of the posterior mandible.
Apposition and remodeling will cause the mandible
to grow larger. (Reynolds et al., 2011; Ghosh et al.,
2009)
The results of this study indicate the maximum
growth of mandibular to lateral direction occurs in
the age group 13-24 years, to reach the optimal size
of bigonial width in the age group 25-34 years. This
is likely due to the mandibular basal bone
morphology generally altered by bone aposition on
the outer (buccal and labial) surfaces of the
mandible to provide a spot of tooth eruption, and
resorption on the lingual surface of the mandible. At
the age after 35 years the mandible will experience a
minimum growth that occurs until age> 60 years
(there is menopause period for the woman) which is
likely due to a greater resorbtion than bone
apposition, especially in the age group> 60 years
who have teeth lost entirely. (Ghosh et al., 2009)
Difference of Bigonial Width Batak Tribe in Medan City According to Age Groups in Terms of Panoramic Radiograph
263
From the transverse aspect, after the first year of
life, the growth in the posterior region of ramus is in
the form of the letter "V". Changes in the function of
chewing muscles, especially in the angle of gonial
regions may also be the cause of the bigger width
increase. The gonial angle is a part of the mandible
that is directly related to the massetter and internal
pteryigoid muscles. During the craniofacial growth
period, the mandible undergoes continuous
repositioning in order to perform optimally function.
The rami grows in divergent direction, in order to
obtain a connection with the maxilla in order to
function normally. (Singh, 2007) A study conducted
by Bishara et al., on the mandible arch, showed
mandibular growth in the lateral direction, with an
increase in 3.7 mm intercanine width between 3-13
years, but decreased by 1.2 mm by 13 to 45 years.
The intermolar width increases by 1.5 mm at the age
between 3-5 years and 1 mm between 8-13 years but
decreases 1 mm at the age of approximately 45
years. (Standring, 2008) The results of this study are
also supported by Leversha et al., examined the
bigonial width that grew from 18-29 years old to 30-
39 years old, and decreased in the 40-49, 50-59, and
60-69 years age group. (Leversha et al., 2015)
In adolescence, there is an increase in the
acceleration of growth, changes in size and shape,
and changes in the proportion of muscle, fat, and
bone. During puberty, there is a considerable
increase in bone mass due to increased bone size
(Sharma et al., 2014) where the rate of bone
formation process is faster than resorption.
However, this growth rate will stop when the linear
growth stops, and bone mass peaks someone is
reached, occurring at the age of 15-25 years. Total
bone mass usually remains constant for about 10
years, because the rate of bone formation and
resorption is balanced. Then the bone mass will
slowly decrease as a result of the dominance of the
resorbsi process in the third decade of life to the
fourth. (Lau et al., 2011)
There was not significant difference in bigonial
width from group 4 (35-60 years) to group 5 (>60
years). This is likely due to the large age range in the
sample used in group 4 (35-60 years). Where the
number of samples used with age 35-40 years as
many as 5 people and ages 41-60 years as many as
25 people, the age at which bone loss is more, and
minimal bone growth. The dominant effect of aging
on bone is the loss of bone mass and strength. At the
age of the third decade to the fourth decade of life,
total bone mass will begin to decline. By age 80, it is
estimated that the body’s total bone mass will be
about 50% of its peak value. Loss of bone mass from
the jaw is caused not only by the teeth, decreased
bone density is caused by the age factor, so the
bones become more fragile. Fractures occur more
easily and the healing process becomes slower. (Lau
et al., 2011; Boskey et al., 2010)
Parathyroid hormone (PTH), an 84-amino acid
peptide secreted by the parathyroid gland is
important as a systemic regulator of calcium
homeostasis, serves to regulate the concentration of
calcium and serum phosphorus through receptor-
mediation, combined actions in the bones, intestines,
and kidneys. High serum PTH levels, increase
osteoclastic bone absorption, as seen in primary and
secondary hyperparathyroidism. Low PTH levels,
increase osteoblastic bone formation, especially if
delivered episodically. The skeletal effect of PTH is
mediated through osteoblasts, because it is the main
expression of PTH receptors. However, osteoblasts
communicate with osteoclasts to mediate the effects
of PTH. Many factors may be involved in increasing
serum PTH levels in the elderly. Vitamin D
deficiency is quite common which can contribute to
elevated serum PTH levels by decreasing calcium
resorption from the gastrointestinal tract. Moreover
estrogen deficiency results in reducing intestinal
calcium absorption as well as renal tubular calcium
disrupted reabsorption, which leads to chronic
negative calcium balance. Vitamin D is an important
factor in the regulation of calcium metabolism. 1,25-
Dihydroxy vitamin D3, the active form of vitamin D
which has the effect of increasing intestinal calcium
absorption, decreasing serum PTH levels through
direct inhibition of PTH secretion, and also
indirectly, through inhibition of PTH secretion with
elevated serum calcium levels. Therefore, vitamin D
has the overall effect of decreasing bone resorption
mediated by PTH. Vitamin D deficiency often
occurs with advanced aging, and this may be another
contributor to the pathogenesis of senile
osteoporosis. Although severe vitamin D deficiency
results in the development of osteomalacia in adults,
mild deficiencies can cause a secondary state of
hyperparathyroidism, with the result of developing
osteoporosis. (Kini et al., 2012; Lau et al., 2011;
Boskey et al., 2010; Feng et al., 2011)
The facial skeleton has a profound effect on one's
appearance. The main characteristic of adolescents is
good skeletal structural support. The result of facial
aging is a combination of soft tissue and bone
changes, with bone loss in certain areas of the facial
bone contributing significantly to aging facial
features. Conceptually it is important to appreciate
that in most individuals with premature aging, facial
frames can be inherently inadequate. Thus, changes
ICNRSD 2018 - International Conference on Natural Resources and Sustainable Development
264
in the facial bone resulting from the aging process
must be resolved to get a natural facial rejuvenation.
(Mendelson et al., 2012)
The mandible is the bone that forms the lower
part of the face, chin, and mandibular angle. The
mandible provides attachment for the mastication
muscles, tongue, and the floor of the mouth. (Burns,
2013) According to Enomoto et al.,, mastication
affects the growth and development of the mandible.
The mechanical stress induced by mastication
greatly affects the condyle cartilage and the
mandible around the mastication muscle, and alters
the growth and development pattern of the mandible.
(Enomoto et al., 2010) Many researches have been
done to evaluate mandibular morphology by age,
such as measurements of height and width of ramus,
condyle height, and bigonial width. The
morphological changes of the mandible after birth
are affected by the teeth (mastication) and age. Age,
systemic factors, and tooth loss may lead to changes
in mandibular morphology. (Liu et al., 2010;
Huumonen et al., 2010; Shaw et al., 2010; Chole et
al., 2013; Shilpa et al., 2014) Increasing age,
changes in the function and structure of mastication
muscles that occur in edentulous patients lead to
reduced contraction in activity and decreased muscle
density compared with toothed patients. The strength
of the masseter and medial pterygoid muscle
contractions that work in the area of the gonial
angle, also affect the basic form of the
mandible.(Thakur et al., 2013; Oksayan et al., 2014)
In computed tomographic scans can be seen the
activity of electromyography and lower muscle
density on the edentulous subject than the dentulous
subject. The occurrence of masticatory muscle
atrophy may be one of the factors that cause
mandibular changes. (Baxter-Jones et al., 2011;
M.Reynolds et al., 2011; Shaw et al., 2010; Chole et
al., 2013; Shilpa et al., 2014) Another factor that
may cause the changes is the loss of intermaxillary
support due to missing teeth, allowing the masseter
and medial pterygoid muscles to draw an
unobstructed pull on the mandible. (Baxter-Jones et
al., 2011) A significant limitation with currently
available uses is data obtained from digital
panoramic radiographs. The ideal study is linear to
show the aging changes in the same individual.
However, the study that can be done in this field is
cross-sectional population research based on the
comparison between individuals in different age
groups, so it cannot see significant changes in the
age-related mandibular of the same individual.
5 CONCLUSION
The conclusion of this study is that group 3 (25-34
years old) has the highest mean value of bigonial
width. There is difference of bigonial width Batak
tribe in Medan according to age group in terms of
panoramic radiography that can be affected by teeth
and age. Statistically significant differences in
bigonial width was group 1 (4-12 years), 2 (13-24
years), and 3 (25-34 years) to the other groups, but
there is not significant differences in bigonial width
for group 4 (35-60 years) to group 5 (>60 years).
ACKNOWLEDGMENT
This research was conducted with the support my
family and all of my friends, Bu Erna from Faculty
of Public Health and Prof. Harlem Marpaung from
Faculty of Math and Science, Universitas Sumatera
Utara.
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