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A R T I C L E I N F O A B S T R A C T
Article history: The aim of this study was to find any relation between soft facial tissue thickness (FSTT) and sex, age and
Received 28 August 2015 asymmetry in the contemporary Czech population. The studied sample consisted of head CT scans of
Received in revised form 11 December 2015 102 adult Czech individuals between the ages of 21 and 83. Forty FSTTs were evaluated and analysed
Accepted 7 January 2016
using PCA, Hotelling’s T2 test, LDA, the Kolmogorov-Smirnov test, MANOVA, the Kruskal-Wallis test and
Available online 15 January 2016
Wilcoxon’s paired test. The greatest sexual dimorphism was detected in the lower part of the face, which
had discriminant power almost the same as the entire faces (approximately 80%). On the other hand, a
Keywords:
significant influence of aging was shown, mostly in the area of the upper face (In females, twice as many
Forensic science
Forensic anthropology population data
landmarks displayed a significant influence, compared with males). The influence of asymmetry was
Craniofacial reconstruction confirmed in seven bilateral landmarks, five of them favouring the right side.
Soft tissue thickness ß 2016 Elsevier Ireland Ltd. All rights reserved.
Computer tomography
Sexual dimorphism
Knowledge of facial soft tissue thicknesses (FSTT) provides the The studies monitoring FSTT are inspired by the assumption of
basis for any craniofacial reconstruction (CFR). The aim of CFR is to the large variability in faces. The reliability of CFR may be
produce a face that matches the underlying skull. This reconstructed negatively influenced by a lack of records about the thickness of
face can help in the recognition of an individual. Craniofacial soft tissues in a specific population. For that reason, many new
reconstruction cannot itself lead to positive identification of human studies have been performed aiming at data collection. Building a
remains; however, it plays an important role in cases in which the database of specimens from various populations to establish the
remains cannot be identified by DNA analysis, fingerprint compari- reference values for FSTT is advantageous; however, it is equally
son or dental record examination [1]. Knowledge of FSTT plays an important to perform studies on a specific population and analyse
important role in other fields as well, for example, embryology or the intra- and inter-population variability.
aesthetic surgery [2]. The appearance of the face is modelled from Foreign studies focus primarily on sex and age dimorphism in
the skeletal remains on the basis of a known average FSTT in specific FSTT. Males typically have higher values than females on almost
anthropometric points [3]. FSTT in reality fluctuates within a specific all landmarks [2,5,7,8]. However, De Greef et al. [9] and Stephan
interval. The final value is dependent on the sex, age, population and Simpson [6] noticed that females reach higher levels of
group and constitution of the subject [4,5], among other aspects. The dimorphism on the cheeks and males near the eyes and mouth
different values are measured in living people and cadavers. Some [9]. Significant differences were found in many studies [e.g.,
methods tend to generate higher values of FSTT; for example, the 2,5,10–12], but greater variation has been detected within one
radiography method generates higher values of FSTT in the medial sex than between sexes [9,13]. The differences between males
plane, and ultrasounds generate higher values on supra-M2, infra- and females are less than 2 mm on average; therefore, they are
M2 or gonion landmarks [6]. The position of scanned subjects can be not crucial for predicting the appearance of a face. Sexual
important as well. Therefore, the comparison of different studies is dimorphism in FSTT does not contribute to facial recognition;
often extremely difficult. however, it plays an important role in the improvement of
CFR [13].
Age-related changes in the face are caused mostly by external
* Corresponding author at: Lublaňská 34, 120 00 Prague 2, Czech Republic.
factors [14,15]. Significant determinants of aging include body
Tel.: +420 221 951 618; fax: +420 221 951 619. mass index, smoking, sun exposure, use of antidepressants,
E-mail address: drgan@seznam.cz (A. Drgáčová). alcohol and drugs consumption and marital status [16–18]. The
http://dx.doi.org/10.1016/j.forsciint.2016.01.011
0379-0738/ß 2016 Elsevier Ireland Ltd. All rights reserved.
106.e2 A. Drgáčová et al. / Forensic Science International 260 (2016) 106.e1–106.e7
appearance of the face is also affected by changes in skeletal wrinkles due to the loss of subcutaneous fat, and gravitation effects
structure and loss of volume in soft tissues [19]. Aging demon- [19]. Unfortunately, these age-related changes are extremely
strates common traits in both sexes, but male faces exhibit more variable and difficult to predict [21].
intense aging changes (Sexually dimorphic traits tended to The asymmetry of FSTT has been the focus of relatively few
diminish in the elderly age category) [20]. The least pronounced studies [e.g., 7,22]. De Greef et al. [23] noted probably the greatest
changes were registered between the ages of 20 and 30, and the influence of asymmetry (50% from select landmarks). However,
most pronounced between the ages of 40 and 50. Soft tissues reveal asymmetry of the face is a commonly accepted fact, which forensic
decreases in facial skin elasticity, the formation of skin folds and papers should therefore consider.
Table 1
Definitions of soft and hard tissue landmarks.
Median Points
Glabella (g) The most anterior midline point on the Glabella’ (g’) The most anterior midline soft tissue point overlying the glabella
frontal bone
Nasion (n) Midline point on the naso-frontal Nasion’ (n’) The most posterior soft tissue point overlying the nasion
suture
Rhinion (rhi) Midline point at the inferior free end of Rhinion’ (rhi’) Midline soft tissue point directly above the hard tissue rhinion
the internasal suture
Spinale (sp) The most anterior midpoint of the Subnasale (sn) Midline point of the angle at the comulella base where the septum
anterior nasal spine of the maxilla and upper lip join
Subspinale (ss) The most posterior midline point on the Subspinale’ (ss’) The most posterior point between soft tissue subnasale and the
premaxilla between the anterior nasal vermilion border of the upper lip in the groove of the philtrum
spine and prosthion
Prosthion (pr) The most anterior point on the Labrale superius (ls) Midline soft tissue point at the vermilion border of upper lip
maxillary alveolar process, between the
central incisor teeth
Infradentale (id) The most anterior point of the alveolar Labrale inferius (li) Midline soft tissue point at the vermilion border of lower lip
process of the mandible
Supramentale (sm) Deepest midline point in the groove Supramentale’ (sm’) Deepest soft tissue point at the midline of the groove just superior
superior to the mental eminence to the chin
Pogonion (pg) The most anterior midline point on the Pogonion’ (pg’) The most anterior midline point on the eminence of the soft tissue
mental eminence of the mandible chin
Gnathion (gn) The most inferior midline point at the Gnathion’ (gn’) Midline soft tissue point directly overlying the gnathion
mental symphysis of the mandible
Bilateral Points
Orbitale superius The most superior point at the Orbitale superius’ (ors’) Soft tissue point directly overlying the hard tissue orbitale
(ors) supraorbital margin superius
Ectoconchion (ec) The most lateral point at the lateral Ectoconchion’ (ec’) Soft tissue point directly overlying the hard tissue ectoconchion
margin of orbit
Orbitale (or) The most inferior point at the Orbitale’ (or’) Soft tissue point directly overlying the hard tissue orbitale
infraorbital margin
Zygion (zy) The most lateral extent of the lateral Zygion’ (zy’) Soft tissue point directly overlying the hard tissue zygion
surface of the zygomatic arch
Jugale (ju) A craniometric point at the union of the Jugale’ (ju’) Soft tissue point directly overlying the hard tissue jugale
temporal and frontal processes of the
zygomatic bone
Inferior malar (im) The deepest point at fossa canina Inferior malar’ (im’) Soft tissue point directly overlying the hard tissue inferior malar
Alare (al) Most lateral point at the border of the Alare’ (al’) The most lateral point at alae nasi
nasal aperture
Supra canine (sC) Point on superior alveolar ridge Supra canine’ (sC’) Soft tissue point directly overlying the hard tissue supra canine
superior to the crown of the maxillary
canine(s)
Infra canine (iC) Point on inferior alveolar ridge inferior Infra canine’ (iC’) Soft tissue point directly overlying the hard tissue infra canine
to the crown of the mandibular
canine(s)
Supra M2 (sM2) Point on superior alveolar ridge Supra M20 (sM20 ) Soft tissue point directly overlying the hard tissue supra M2
superior to the crown of the maxillary
second molar(s)
Infra M2 (iM2) Point on inferior alveolar ridge inferior Infra M20 (iM20 ) Soft tissue point directly overlying the hard tissue infra M2
to the crown of the mandibular second
molar(s)
Gonion (go) Point on the lateral aspect of the border Gonion’ (go’) Soft tissue point directly overlying the hard tissue gonion
of mandibular angle where a tangent
bisects the angle formed by the
posterior ramus border and the inferior
corpus border
Mentale (m) The most inferior point at border of Mentale’ (m’) Soft tissue point directly overlying the hard tissue mentale
foramen mentale
Mid-ramus (mr) Point at the center of the mandibular Mid-ramus’ (mr’) Soft tissue point directly overlying the hard tissue mid-ramus
ramus
Mid-mandibular Point on the inferior border of the Mid-mandibular Soft tissue point directly overlying the hard tissue mid-
border (mmb) corpus of the mandible midway border’ (mmb’) mandibular border
between pogonion and gonion
A. Drgáčová et al. / Forensic Science International 260 (2016) 106.e1–106.e7 106.e3
Our research was based on the measurement of soft tissue the medial plane were defined on the hard and soft profiles
depth using CT scans of 102 Czech adult individuals between the separately. Bilateral points were defined initially on the skull, and
ages of 21 and 83. The aim of this study was to determine the mean the corresponding soft tissue landmarks were found in locations
and variability of FSTT in Czech adults and to expand the Central proximate to the craniometric landmarks. The only exception was
European population FSTT sample. Our analyses were evaluated the point alare, which was always placed on soft and hard tissues
with respect to sex, age and bilateral asymmetry of the face. separately. Landmark placement was performed by the first
author using the in-house software Morphome3cs (https://
1. Material and methods www.natur.cuni.cz/biology/anthropology/veda-a-vyzkum/
morphome3cs-ii-en?set_language=en). Morphome3cs uses a ray
Our study was performed using CT scans from 102 adults, casting approach to place landmarks on an isosurface with a
including 56 males and 46 females. None of the patients had any defined density (http://www.cs.utah.edu/shirley/papers/iso/iso.
facial malformations [24], and the data were anonymous, tagged pdf). Thresholds for soft and hard tissues were set to 700 HU and
only with the age and sex of the patients. All individuals were 226 HU, respectively (http://mspace.lib.umanitoba.ca/xmlui/
treated at the Department of Radiology in Na Homolce Hospital, bitstream/handle/1993/22023/Maltais%20Lapointe_Genevieve.
Prague. Surface models of the heads were created using pdf?sequence=1). The measurements were taken perpendicular to
reconstruction methods that employed virtual 3-D modelling the craniometric points, following Vanezis [25] and Panenková
from the Digital Imaging and Communications in Medicine et al. [8]; the FSTT equals the length of the line projecting from the
(DICOM) image sequence of the CT outputs. The initial raw data skeletal to the facial point.
were acquired by scanning the heads of patients using a Somatom A complete set of landmarks was defined in only 54 speci-
Sensation 16 tomograph (Siemens, Erlangen, Germany). The slice mens. In some scans, landmark placement was impossible due to
distance was 0.75 mm (0.4 mm kernel, H60). Patients gave beam-hardening artefacts caused by dental fillings. Therefore,
informed consent for the use of their CT images and data in this the data were split into 3 sets: data using all landmarks (31 males
study. The sample ranged in age from 21 to 83 years and was and 23 females), data with the upper part of the face only
divided into three age groups: 20–39 years, 40–59 years, and above (55 males and 45 females) and data with the lower part of the
60 years. face (32 males and 23 females). The division of face is illustrated
Soft tissue depth was measured at 40 standard anthropological in Fig. 1.
landmarks on the head (see Table 1). The position of every
landmark was controlled in relation to three planes. The points in
Fig. 1. The complete set of landmarks. The line separates the face to upper and lower Fig. 2. The results of sexual dimorphism of FSTT. The significant FSTT are displayed
part. by full points.
106.e4 A. Drgáčová et al. / Forensic Science International 260 (2016) 106.e1–106.e7
Measurement error was determined according to [26], using Morphome3cs (Faculty of Mathematics and Physics of Charles
5 repeated measurements of 5 specimens. The mean measurement University, Prague). The results were compared with Panenkova
error was 0.778 mm. et al. [8] because of the geographical relationship between the
General descriptive statistics were calculated first. Variability of samples.
sex was tested using a non-parametric Kolmogorov-Smirnov test.
Principal component analysis (PCA) was performed on all three 2. Results
sets. The first principal components were selected and tested using
Shapiro Wilk’s normality W test, Hotteling’s T2 test and linear 2.1. Sexual dimorphism
discriminant analysis (LDA). Scores on the first three principal
components were used for LDA, and this number was tested using The results with regard to sexual dimorphism in FSTT are
the broken-stick rule. The effect of age on tissue thickness was shown in Table 2 and Fig. 2. Landmarks with significant sexually
evaluated using the Kruskal Wallis test performed separately on dimorphic FSTT were situated primarily on the A lower part of the
each linear measurement and using multivariate analysis of face (all lower face landmarks with the exception of the mid-
variance (MANOVA) applied to the first three principal compo- mandibular border, gonion and infra M2 on the right side).
nents. The significance of soft tissue depth asymmetry at bilateral Significant FSTTs were detected also at almost all landmarks on or
points was tested using Wilcoxon’s paired test. Statistical near the midline, with the exception of glabella, and at nine
significance was set at a = 0.05. bilateral landmarks (mentale, supra canine, infra canine, supra M2,
All data were analysed using Microsoft Excel (Microsoft infra M2 on the left side, alare, orbitale, orbitale superius and mid-
Corporation), PAST 1.99 (Natural History Museum, Oslo) and ramus). All significant soft tissue thicknesses are higher in males.
Table 2
The results of sex dimorphism (Kolmogorov-Smirnov test).
Glabella 46 3.662 9.505 6.019 1.315 0.506 56 3.991 9.659 6.298 1.165 0.022 0.155
Nasion 46 5.173 14.595 8.255 1.868 0.082 56 3.831 12.900 9.416 1.905 0.125 0.003*
Rhinion 46 1.587 4.766 2.618 0.627 0.009 56 2.168 4.690 3.115 0.633 0.001 0.004*
Spinale-Subnasale 46 6.723 14.458 9.848 1.947 0.022 56 7.206 19.019 11.518 2.255 0.013 0.001*
Subspinale 46 9.867 16.838 12.765 1.773 0.325 56 11.792 19.825 15.655 1.803 0.311 <0.001*
Prosthion-Labrale 43 7.462 17.335 11.128 1.966 0.230 47 4.312 20.638 13.707 2.689 0.216 <0.001*
superius
Infradentale-Labrale 43 9.716 18.215 14.151 1.962 0.773 49 12.24 23.871 16.351 2.104 0.096 <0.001*
inferius
Supramentale 46 8.513 14.642 10.939 1.420 0.049 56 10.061 16.602 12.514 1.559 0.004 <0.001*
Pogonion 46 7.309 17.384 11.767 2.197 0.671 56 7.510 22.995 13.542 2.641 0.004 0.002*
Gnathion 41 4.942 13.526 7.978 2.155 0.106 52 4.921 13.512 9.148 1.876 0.132 0.014*
Mentale (R) 46 6.063 18.029 12.053 2.430 0.925 56 9.988 19.193 14.170 2.081 0.177 <0.001*
Mentale (L) 46 6.057 16.885 11.560 2.386 0.668 56 8.891 17.737 13.342 2.229 0.060 0.003*
Gonion (R) 46 5.401 28.492 15.948 6.224 0.123 56 6.861 33.597 17.941 6.206 0.064 0.060
Gonion (L) 46 4.804 31.534 16.152 6.808 0.344 56 7.476 34.858 17.998 6.170 0.019 0.181
Supra canine (R) 40 5.318 12.725 8.438 1.762 0.323 47 7.417 15.657 11.035 1.679 0.641 <0.001*
Supra canine (L) 41 5.943 13.278 8.640 1.632 0.150 47 7.530 15.595 10.844 1.841 0.301 <0.001*
Infra canine (R) 43 5.898 13.672 9.316 1.724 0.022 50 6.701 14.846 10.476 1.913 0.142 0.002*
Infra canine (L) 43 6.215 13.394 8.943 1.713 0.003 50 6.845 15.208 9.947 1.825 0.018 0.013*
Supra M2 (R) 34 21.535 45.605 29.626 5.965 0.016 39 25.815 42.700 33.530 4.988 0.009 0.001*
Supra M2 (L) 34 19.707 40.365 29.414 4.823 0.657 39 24.638 46.431 32.162 4.765 0.071 0.041*
Infra M2 (R) 31 21.535 36.852 25.519 6.096 0.071 37 19.111 36.551 27.107 4.979 0.088 0.060
Infra M2 (L) 30 14.859 37.853 24.838 6.346 0.030 37 18.784 37.776 26.793 4.478 0.111 0.006*
Alare (R) 46 8.498 14.724 10.623 1.282 0.075 56 8.776 19.821 12.02 1.668 0.000 <0.001*
Alare (L) 46 7.681 14.778 10.690 1.401 0.812 56 8.667 21.929 12.357 1.985 0.000 <0.001*
Orbitale (R) 46 3.022 12.953 7.229 2.301 0.237 56 3.677 15.007 8.350 3.005 0.001 0.230
Orbitale (L) 46 2.897 12.648 7.479 2.547 0.133 56 3.596 16.169 8.370 3.204 0.000 0.593
Zygion (R) 46 4.556 14.586 9.174 2.882 0.016 56 4.315 17.680 8.491 2.440 0.002 0.357
Zygion (L) 46 4.718 16.839 9.197 3.164 0.024 56 4.934 16.300 8.770 2.874 0.000 0.322
Jugale (R) 46 6.555 16.489 10.565 2.458 0.026 56 6.048 15.095 10.367 2.372 0.001 0.458
Jugale (L) 46 6.007 16.630 10.270 2.554 0.061 56 5.128 16.134 9.721 2.532 0.005 0.607
Ectoconchion (R) 46 2.558 10.134 5.879 1.752 0.704 56 3.109 9.740 5.847 1.684 0.003 0.919
Ectoconchion (L) 46 3.244 9.858 5.857 1.560 0.026 56 3.262 9.946 5.856 1.767 0.000 0.540
Orbitale superius (R) 46 5.444 12.588 8.935 1.587 0.975 56 5.924 13.974 10.221 1.693 0.078 0.001*
Orbitale superius (L) 46 4.878 12.032 8.911 1.776 0.338 56 5.224 13.433 9.996 1.716 0.106 0.008*
Inferior malar (R) 46 11.826 35.187 17.460 3.826 0.000 56 10.794 26.948 18.060 3.123 0.023 0.136
Inferior malar (L) 46 13.577 25.723 17.913 2.651 0.090 56 11.898 25.769 18.200 2.864 0.068 0.872
Mid-ramus (R) 46 14.448 40.158 23.040 4.809 0.013 56 17.468 36.164 25.892 4.230 0.722 0.017*
Mid-ramus (L) 46 14.706 37.477 22.824 4.689 0.045 56 18.432 33.714 25.441 3.877 0.168 0.006*
Mid-mandibular 46 7.253 23.101 13.149 3.804 0.319 56 6.164 23.029 13.220 3.740 0.073 0.992
border (R)
Mid-mandibular 46 7.166 26.409 14.215 4.091 0.128 56 6.763 22.444 13.566 3.738 0.336 0.573
border (L)
Table 3
The results of LDA.
Part of face Success Number of successful Number of Success rate of Number of successful Number of
rate classifications (F/M) unsuccessful clasification with classifications (F/M) unsuccessful
classifications (F/M) cross-validation classifications (F/M)
% n % n % % N % n %
All face 85.19 19/27 82.61/87.10 4/4 17.39/12.90 81.48 18/25 78.26/80.65 5/6 21.74/19.35
Upper part of face 65.00 26/39 57.78/70.91 19/16 42.22/29.09 62.00 26/36 57.78/65.45 19/19 42.22/34.55
Lower part of face 87.27 18/30 78.26/93.75 5/2 21.74/6.25 80.00 17/27 73.91/84.38 6/5 26.09/15.62
Fig. 3. The results of age influence on FSTT variability (females on the left side, males on the right sides). The significant FSTT are displayed by full points.
On the basis of these results, sex classification using FSTT was The values in the buccal area (orbitale, jugale and inferior malar)
evaluated (see Table 3). The accuracy of sex classification was increased from the ages of 21 to 59 and then decreased. The
tested three times (for the face as a whole, the upper part of face significant values were often detected in the upper part of face for
and the lower part of face) using Hotelling’s T2 test and LDA with both sexes. This result was confirmed using MANOVA (p < 0.001).
cross-validation. Significant sexual dimorphism in FSTT was
detected for all groups (for the entire face p < 0.001, for the upper Table 4
part of face p = 0.004, and for the lower part of face p < 0.001). The The results of asymmetry (Wilcoxon’s paired test).
most accurate classification was obtained using all FSTT landmarks Landmark n Mean Mean Wilcoxon
(81.48%), but the discriminant power of only the lower face FSTT (mm) (mm) paired test
landmarks was almost the same (80%). Using landmarks in the (p-value)
upper part of face, the classification success rate dropped to 62%. Mentale 102 13.215 12.556 <0.001*
Gonion 102 17.042 17.176 0.673
2.2. Age Supra canine 87 9.863 9.797 0.498
Infra canine 93 9.947 9.502 <0.001*
Supra M2 71 31.773 30.682 0.009*
The results with regard to the influence of age on FSTT Infra M2 66 26.432 26.050 0.042*
variability are shown in Fig. 3. Twice as many landmarks with Alare 102 11.390 11.598 0.088
significant age influence were detected in females (glabella, Orbitale 102 7.844 7.968 0.420
subspinale, gonion, orbitale, zygion, jugale, inferior malar on the Zygion 102 8.799 8.960 0.702
Jugale 102 10.456 9.969 <0.001*
right side only, mid-ramus on the left side only and mid-
Ectoconchion 102 5.861 5.856 0.680
mandibular border). In males, age had a significant effect on Orbitale superius 102 9.635 9.502 0.090
4 landmarks (supramentale, orbitale, ectoconchion on the left side Inferior malar 101 17.808 18.059 0.042*
only and mid-ramus on the left side only). The FSTT values for Mid-ramus 102 24.621 24.275 0.077
males always increased with age. The FSTT values for females Mid-mandibular border 102 13.188 13.862 0.003*
Table 5 Table 6
Comparison of results with study Panenkova et al. [8]. Comparison of results with study Guyomarc’h et al. [28].
Sex N Mean (SD) N Mean (SD) P-value N Mean (SD) N Mean (SD) P-value
Glabella M 56 6.3 (1.2) 80 5.9 (1.3) 0.071 Glabella 102 6.2 (1.2) 366 6.5 (1.2) 0.026*
F 46 6.0 (1.3) 80 5.5 (1.0) 0.017* Nasion 102 8.9 (1.9) 469 8.2 (1.6) <0.001*
Nasion M 56 9.4 (1.9) 80 8.0 (1.5) <0.001* Rhinion 101 2.9 (0.7) 321 3.0 (1.3) 0.458
F 46 8.3 (1.9) 80 6.9 (1.2) <0.001* Subspinale 101 14.4 (2.3) 459 12.9 (0.9) <0.001*
Rhinion M 56 3.1 (0.6) 80 2.5 (0.7) <0.001* Prosthion/labrale 84 12.4 (2.7) 294 14.1 (2.5) <0.001*
F 46 2.6 (0.6) 80 2.1 (0.6) <0.001* superius
Subspinale M 56 15.7 (1.8) 69 15.2 (2.6) 0.225 Infradentale/labrale 90 15.3 (2.3) 266 16.8 (3.1) <0.001*
F 46 12.8 (1.8) 72 12.4 (2.0) 0.273 inferius
Prosthion/labrale M 47 13.7 (2.7) 21 12.9 (1.9) 0.224 Pogonion 102 12.7 (2.6) 254 11.8 (2.1) <0.001*
superius Gnathion 93 8.6 (2.1) 211 9.5 (3.3) <0.001*
F 43 11.1 (1.9) 12 11.4 (1.9) 0.628 Orbitale 102 7.8 (2.8) 371 8.6 (2.3) 0.003*
Orbitale superius M 56 10.2 (1.7) 80 8.2 (1.6) <0.001* Ectokonchion 102 5.9 (1.7) 372 7.8 (2.6) <0.001*
F 46 8.9 (1.8) 80 7.2 (1.3) <0.001* Zygion 102 8.8 (2.7) 364 10.0 (2.8) <0.001*
Orbitale M 56 8.4 (3.0) 80 7.0 (2.1) 0.002* Jugale 102 10.5 (2.4) 245 10.9 (2.2) 0.134
F 46 7.2 (2.3) 80 6.8 (2.5) 0.375 Gonion 102 17.0 (6.3) 238 18.5 (6.9) 0.060
Ektokonchion M 56 5.8 (1.7) 79 9.0 (2.0) <0.001* Supra canine 82 9.9 (2.1) 307 13.4 (2.6) <0.001*
F 46 5.9 (1.8) 80 10.0 (2.0) <0.001* Infra canine 92 9.9 (1.9) 262 12.8 (2.1) <0.001*
Zygion M 56 8.5 (2.4) 75 9.5 (2.4) 0.019* Mentale 102 13.2 (2.5) 255 12.8 (2.1) 0.125
F 46 9.2 (2.9) 66 9.1 (2.5) 0.846 Mid-ramus 101 24.6 (4.7) 327 22.7 (4.8) <0.001*
Inferior malar M 56 18.1 (3.1) 75 16.4 (2.5) <0.001* Mid-mandibular 101 13.2 (3.8) 242 14.6 (4.3) 0.005*
F 46 17.5 (3.8) 74 15.2 (2.5) <0.001* border
Supra M2 M 39 33.5 (4.9) 60 30.6 (5.2) 0.007* *
p < 0.05.
F 34 29.6 (5.9) 57 28.1 (4.8) 0.189
*
p < 0.05.