Anthropological Review Vol. 85(3), 1–18 (2022)

Anthropological Review

Available online at: https://doi.org/10.18778/1898-6773.85.3.01



Mandibular Canal and the Arrangement of the Neurovascular Bundle Exit Routes in Divergent Populations


Agnieszka Tomaszewska*

Department of Anthropology, Wroclaw University of Environmental and Life Sciences, Poland

Daniel Psonak

Department of Human Biology, Department of Biological Sciences, University of Wroclaw, Poland

Joanna Rudzka

Department of Human Biology, Department of Biological Sciences, University of Wroclaw, Poland




ABSTRACT: Aim: In face anatomy and surgery, variation in the presence, number, location, and size of the mental foramen is discussed. Knowledge of the location of the mental foramen canal, which may led due to the possibility of accidental injury of the neurovascular bundle passing through this canal may lead to anesthesia. This study aimed to present selected anatomical features of human mandibles, focusing on the morphology of the mandibular canal and its neurovascular bundle exit in populations with different socio-economic status.

Material and methods: Selected well preserved and unharmed human skulls (N= 169) (50.3% males, 49.7% females) from two populations (rural and outskirts) from Poland were used. Populations differed in socioeconomic statuses.

Results: Obvious dimorphic differences in each analyzed population were stated and inter-population differences were observed as well. In an outskirt population sexual dimorphism was more evident. Those differences should be considered when approaching the mandibular canal during anesthetic, surgical and forensic procedures.

Discussion: The occurrence of the mental foramen is relatively constant, but location is variable, and thus, each individual may exhibit a different arrangement of bundle exits. Both the position and the direction of the exit of the neurovascular bundle were similar to other European population. However, differences in localization between those two investigated populations were observed. This may suggest that not only genetic but also environmental factors, such as living conditions and diet (which affects developmental stability), may influence the morphology of the mandibular features.

KEY WORDS: cranial openings, mental foramen, mandibular foramen, canal mandible.



Introduction

Knowledge of the localization of the craniofacial foramina is of importance, mainly for dental, surgical, anesthetic and cosmetic procedures concerning the human skull (Cutright et al. 2003). Among the variety of skull foramina, mental and mandibular foramina are of greatest interest in both clinical and diagnostic practices.

The human mandible is the largest, strongest, and lowest bone in the face. Its innervation is provided by inferior alveolar nerve, a branch of the mandibular division of trigeminal (CNV) nerve (nervus trigeminus), which may be impaired due to, e.g. an accidental injury during dental or surgical procedures. A lesion to CNV may lead to local anesthesia, i.e., half of the mandibular region in the case of branches of the inferior alveolar nerve division (Gray 1985), which is described in detail by Renton et al. (2010).

The functional complexity of the human mandible has contributed to its complex structure, in which foramina and canals responsible for communication between the spaces within the human skull can be distinguished. The mandibular foramen is located in the middle of the mandibular ramus, in the inner (medial) aspect of the mandible. The mental foramen is located lateral to the mental protuberance, usually inferior to the apices of the mandibular first and second premolars. The mental foramen allows entrance of the mental nerve and blood vessels into the mandibular canal (Valente et al. 2012; Łasinski 1993; Samantha and Kharb 2013). Through the mandibular canal runs the inferior alveolar nerve and inferior alveolar artery, which provides blood supply to the lower teeth, periodonts of the buccal side and chin and lower lip (Gray 1985; Drake et al. 2010).

Inter- populations and regional differences in size and location of the mental and mandibular foramina has been reported (Green 1987; Moiseiwitsch and Hill 1998; Nayarana and Prashanthi 2003; Hasan 2012; Shenoy et al. 2012). Thus, its position, size, and number need to be considered before preparing osteotomy and other surgical procedures in the foraminal area. Although different methods of measurements of the mandibular features have been reported, the traditional anthropometric measurements with sliding calipers are most often carried out. However, some research was conducted on roentgenographs. Therefore, we should be aware of small simplification of the obtained measurements, because the results are in 2 D space, and therefore, some of the curvilinear measurements may be simplified. Moreover, anatomical variations may impede observations of some mandibular features, such as the bifid or trifid mandibular canal (Mizbah et al. 2012; Miličević et al. 2021), which may not be detected in panoramic or periapical films (Dario 2002). Its occurrence depends on the assessment method (cone- beam computed tomography or panoramic radiographs) but for anthropological and archaeological field work purposes only macroscopic assessment is useable. Radiographic assessment of mental and mandibular foramina may be tentative. Jacobs et al. (2004) reported the mental foramen was detected on 94% of panoramic radiographs, but clear visibility was only attained in only 49% of the time. Similarly, Yosue and Brooks (1989) observed the mental foramen in 87.5% of the samples, but the foramina were clearly visible only in 64% of the samples. Therefore, computed tomography seems to be the best solution in visualizing the position of the foraminal area. According to Sonick et al. (1994), average linear errors for CT investigation is only 1.8% (compared to 24% for panoramic films and 14% for periapical films).

This study aims to compare selected anatomical features of human mandibles, focusing on the morphology of the mental and mandibular foramina. Since there have been reported inter-populations and regional differences in mandibular morphology, we used 2 populations with different socioeconomic statuses to determine whether environmental (geographical) conditions, e.g., life conditions and diet (which affects developmental stability) in diverse populations can influence the morphology of the mandibular features. This study makes also clinical suggestions to reduce inadvertent damage to the mental and inferior alveolar nerve during surgical procedures or dental approaches in the foraminal area.

Material and methods

The study used 169 adult skulls, held at the Department of Human Biology, University of Wroclaw, Poland. The adult age of the crania was confirmed based on the closure of sphenooccipital synchondrosis. The sex of the individuals was determined based on sexually dimorphic cranial features (Workshop 1980). None of the examined skulls showed signs of cranial deformations, malformations, or trauma.

For the analysis, a selection of 2 populations from the Middle-Western European region with different socioeconomic statuses, were used:

  1. An example of the rural population sample from Sypniewo site (Maków County, Masovian Voivodeship, Poland) (Xth – XIIIth centuries) (Sekutowski 2002; Biermann 2006). This sample consisted of 75 skulls 25 (33.0%) skulls which were classified as male and 50 (67.0%) as female.
  2. An example of the outskirt population sample from Gródek upon the Bug River (Hrubieszów County, Lublin Voivodeship, Poland) (Xth- XIIIth centuries) was examined (Belniak et al., 1961). The sample consisted of 94 skulls 60 (64.0%) classified as male and 34 (36.0%) as female.

Morphometric measurements were conducted using a MicroScribe G2L, a 3D contact scanner (www.e-microscribe.com). The measurements (Tab. 1, Fig. 1) were carried out according to Martin’s instructions (Martin et al. 1988) and recorded to two decimal places of a millimeter. Each measurement was conducted twice and an average of 2 measurements was used for statistical analyses using Statistica 13.0 software (StatSoft 2016).

The mean, standard deviation (SD), and variation ranges (minimum-maximum) for each of the measurements were calculated. All variables had a normal distribution (Shapiro–Wilk test; p>0.05), mostly with homogeneous variances (Levene’s test; p>0.05). For paired comparisons, the Student t-test was used (in cases where variances were not homogenous- with Cochran-Cox adjustment) or Wilcoxon test as an alternative. For unpaired comparisons, as an alternative, the U-Mann Whitney test was used. Pearson correlation coefficient (or Spearman for non- normal distribution of the features) was also calculated. The scale according to Stanisz (1998) was used to apply the strength of the correlation:

0 < r < 0.1 very weak correlation

0.1 ≤ r < 0.3 weak correlation

0.3 ≤ r < 0.5 average correlation

0.5 ≤ r < 0.7 high correlation

0.7 ≤ r < 0.9 very height correlation

0.9 ≤ r < 1 almost complete correlation.

Table 1. Measurements taken in the study sample
Martin’s et al. (1988) measurement number Measurements Description of measurements Figure 1- measurement number
65 kdl-kdl intercondylar breadth 1–1
65(1) kr-kr distance between coronoid processes 2–2
66 go-go gonion- gonion distance 3–3
68 gn-go gnathion- gonion distance 4–3
69 id-gn infradentale- gnathion distance 4–5
69(2) CHM2 mandibular corpus height below second molar 13
70 go-cm mandibular ramus height gonion- caput mandibulae
70(3) MID mandibular incisura depth 8
79 MA mandibular angle 7
kdl-kr distance between condylar and coronoid processes 1–2
pg- gn pogonion- gnathion distance 6–4
id- pg infradentale- pogonion distance 5–6
pg- ml pogonion- formane mentale distance 6–9
MinCH minimal corpus height 10
MaxCH maximal corpus height 11
MinMB minimal mandibular breadth
MaxMB maximal mandibular breadth
FMeB mental foramen breadth 9
FMaB mandibular foramen breadth 12
mb- ml mandibular foramen and mental foramen distance (mandibular canal length)

Obraz zawierający wewnątrz

Opis wygenerowany automatycznie

Fig. 1. Measurements taken in the study sample (numbers described in Table 1) (www.legacy.owensboro.kctcs.edu)

Sexual dimorphism was calculated using the formula, where:

SexDim = [(X̅mX̅f) : X̅f] × 100%,

X̅m – male mean, X̅f – female mean.

The significance level was taken at p<0.05 (Stanisz 1998; Field 2006).

Results

For the Sypniewo and Gródek upon the Bug River samples, for unpaired features, significant differences between those two investigated populations were found for 8 features. For the population from the Gródek upon Bug River all features had higher values than those in the Sypniewo population (except for id-pg, go-cm, and MA, although not significant) (Tab. 2).

Table 2. Differences between two analysed populations (bilateral features were averaged)
Features Sypniewo Gródek upon the Bug Test Z Test t Df p

X̅

SD N

X̅

SD N
go-go 95.8 7.1 38 100.5 7.4 41 2.68 p3=0.001*
pg-gn 14.0 1.8 73 15.7 2.1 91 5.37 p3<0.001*
id-gn 24.0 3.5 68 25.3 3.3 87 2.4 153 p1<0.001*
id-pg 9.9 2.8 68 9.9 2.4 87 3.36 p3= 0.920
kdl-kdl 117.7 5.2 29 119.7 6.3 49 4.66 p3=0.110
kr-kr 95.3 6.0 51 97.9 9.9 64 3.81 p3<0.001*
gn-go 79.1 4.5 55 81.7 7.0 86 3.04 p2=0.002*
pg-FMeB 23.9 2.6 74 24.4 4.0 92 0.38 p2=0.703
CHM2 21.4 3.2 57 22.0 4.0 89 0.64 p2=0.526
MINMH 18.2 4.5 57 19.9 5.1 91 1.06 p2=0.289
MAXMH 22.3 5.5 57 24.4 5.9 91 1.04 p2=0.263
kdl-kr 42.2 4.0 57 43.0 4.6 87 1.05 p2=0.292
MID 12.1 1.4 55 12.5 1.9 84 2.37 p2=0.018*
MA 138.2 5.6 50 135.3 6.8 86 1.9 p2=0.058
MinMB 11.1 1.4 75 12.0 1.5 94 1.28 p2=0.202
MaxMB 14.6 1.6 75 15.4 1.6 94 2.38 p2=0.017*
mb-ml 56.7 3.8 73 59.0 4.0 88 1.55 p2=0.120
FMeB 3.4 1.2 75 3.9 0.9 94 2.42 p2=0.016*
FMaB 2.7 0.6 74 3.5 1.7 92 0.05 p2=0.960
go-cm 60.2 6.6 49 59.2 9.9 77 0.14 p2=0.889
p2- Wilcoxon’s test, p3- U-Manna Whitney’s test

After controlling for sex, even more features were found to differ significantly. Sexual dimorphism for Sypniewo population was 7.0% and for Gródek upon the Bug River 7.5%. Descriptive statistics are presented in Tables 3 and 4 for Sypniewo and Gródek located along the Bug River respectively. Right and left side measurements were higher for males in both populations (except for FMaB in the Sypniewo sample) (Tab. 3 and 4). Comparisons of bilateral features has revealed significant differences in both sexes for few features, but only in the population from the Gródek upon the Bug River (Tab. 5). In contrast, in the Sypniewo sample, no significant differences between sides were observed.

Table 3. Descriptive statistics for male and female skulls in the Sypniewo population [in mm]
Features Body side FEMALES MALES Test Z** Test C* df p
X̅ SD N Ranges min-max X̅ SD N Ranges min-max
go-go 94.1 7.4 22 85-114 98.2 6.3 16 90-107
pg-gn 13.4 1.5 50 11-17 15.3 1.7 23 11-18 4.09 <0.01
id-gn 23.1 2.9 46 16-29 26.1 3.9 22 19-34 3.53 66 <0.01
id-pg 9.4 2.5 46 4-16 10.7 3.2 22 5-17
kdl-kdl 115.2 3.8 18 110-125 121.9 4.7 11 112-129 3.12 <0.01
kr-kr 94.1 5.6 35 82-105 97.9 6.3 16 85-106 2.14 49 0.037
gn-go right 77.5 3.7 30 70-86 80.9 4.2 21 74-89 2.99 49 <0.01
gn-go left 78.0 4.3 24 70-86 80.9 5.5 19 72-90 2.00 0.045
pg-FMeB right 23.6 1.8 49 19-29 25.3 1.5 24 23-29 3.73 <0.01
pg-FMeB left 23.9 1.7 49 19-27 25.1 1.3 24 22-28 2.74 0.06
CHM2 right 20.7 3.1 37 15-26 23.0 3.6 19 16-31 2.41 0.016
CHM2 left 20.5 3.0 36 16-29 22.6 3.4 15 16-28
MinMH right 19.5 2.8 37 12-24 21.7 3.4 18 17-29 2.12 0.034
MinMH left 19.1 2.1 36 15-24 21.8 2.6 12 17-25
MaxMH right 23.8 2.5 37 17-29 27.3 3.7 18 22-34 3.30 <0.001
MaxMH left 23.9 2.8 36 19-31 26.4 4.1 12 20-34 <0.001
kdl-kr right 41.2 3.3 29 35-48 43.2 4.7 16 36-50
kdl-kr left 41.7 3.7 28 34-49 43.5 4.4 14 37-50
MID right 12.0 1.4 26 10-15 12.8 1.5 15 10-15
MID left 11.9 1.2 27 10-14 12.4 1.8 14 9-15
MA right 138.0 5.2 23 129-147 138.6 6.5 18 130-152
MA left 138.2 5.0 18 130-147 138.4 6.9 14 128-153
Min MB right 10.8 1.4 49 8-14 11.9 1.4 25 10-14 2.71 0.007
MinMB left 10.7 1.1 49 8-14 11.8 1.8 24 9-16 <0.001
MaxMB right 14.4 1.8 49 10-17 14.7 1.5 25 11-18 2.73 0.006
MaxMB left 14.5 1.7 49 10-18 15.1 1.6 24 12-19 5.69 68 0.001
Mb-ml right 55.0 2.5 48 50-61 59.4 3.8 22 51-66 5.03 62 <0.001
Mb-ml left 55.4 2.8 43 46-61 59.8 4.1 21 52-67 <0.001
FMeB right 3.4 1.3 50 1-6 3.6 1.4 24 2-7
FMeB left 3.3 1.3 49 1-7 3.2 1.3 25 1-21
FMaB right 2.7 0.6 48 2-4 2.9 0.9 23 2-5
FMaB left 2.8 0.5 45 2-4 2.7 0.8 21 1-4
go-cm right 59.0 3.6 22 52-67 64.7 4.4 17 59-73 4.52 37 <0.001
go-cm left 57.8 3.8 18 50-65 64.1 4.8 14 58-73 4.18 30 <0.001
*Test C- Cochran- Cox’ adjustment; **Test z- U Mann- Whitney test
Table 4. Descriptive statistics for male and female skulls in the Gródek upon the Bug River population [in mm]
Features Body side FEMALES MALES Test Z** Test C* df p
X̅ SD N Ranges min-max X̅ SD N Ranges min-max
go-go 98.2 5.5 15 90-106 101.9 8.2 26 84-115
pg-gn 15.1 1.8 33 11-18 16.1 2.2 58 11-22 2.29 89 0.024
id-gn 23.8 2.4 31 19-29 26.2 3.4 56 17-32 3.48 85 0.001
id-pg 8.8 2.3 31 5-14 10.5 2.3 56 5-17 3.10 0.002
kdl-kdl 116.3 4.3 21 106-126 122.3 6.5 28 106-133 3.66 47 0.001
kr-kr 94.7 13.3 26 34-108 100.1 6.0 38 85-111 2.15 0.032
gn-go right 82.1 6.4 17 73-93 83.4 6.5 40 74-100 2.00 0.045
gn-go left 79.8 6.0 28 73-99 82.5 5.8 40 71-96
pg-FMeB right 25.1 2.0 31 22-28 25.5 2.2 57 21-30
pg-FMeB left 25.3 1.9 32 21-29 25.6 2.2 57 23-31
CHM2 right 21.3 2.8 29 15-27 22.9 3.3 51 15-29 2.42 82 0.018
CHM2 left 21.5 2.4 32 16-26 23.1 3.2 52 17-30
MinMH right 20.9 2.3 28 17-27 22.6 3.3 52 12-31 2.46 78 0.016
MinMH left 21.6 2.1 31 18-26 22.1 3.0 54 12-27
MaxMH right 25.5 2.3 29 22-32 27.9 3.0 52 21-33 3.66 <0.001
MaxMH left 25.7 2.5 30 22-33 27.3 2.8 54 22-33 2.51 0.012
kdl-kr right 40.9 3.7 27 32-47 44.2 3.8 46 36-52 3.43 <0.001
kdl-kr left 41.4 3.9 27 33-48 44.7 3.4 44 36-50 3.30 <0.001
MID right 12.0 1.4 24 10-15 12.8 2.2 45 9-18
MID left 11.7 1.6 28 9-15 13.3 2.2 38 9-20 3.02 0.003
MA right 137.5 6.5 17 126-150 134.0 8.0 40 106-145
MA left 136.5 7.2 29 123-150 135.5 7.0 39 119-151
Min MB right 11.2 1.1 33 9-14 12.6 1.5 58 9-16 4.41 0.003
MinMB left 11.2 1.3 32 9-14 12.4 1.6 59 9-16 3.26 0.001
MaxMB right 14.7 1.2 33 12-17 15.6 1.8 58 12-20 2.09 0.036
MaxMB left 15.1 1.2 32 13-17 15.9 1.7 59 12-21 2.57 <0.010
Mb-ml right 56.6 3.9 30 48-63 60.0 4.1 52 52-68 3.09 <0.001
Mb-ml left 57.6 4.1 30 50-66 60.2 4.3 50 47-69 2.68 78 <0.001
FMeB right 3.7 0.8 32 2-6 4.0 1.0 59 2-6
FMeB left 3.7 1.0 33 2-6 3.8 1.0 58 2-6
FMaB right 3.1 0.9 31 2-5 4.0 3.9 52 2-31
FMaB left 3.0 0.8 30 2-5 3.6 0.9 50 2-6 2.43 0.015
go-cm right 59.3 3.3 16 52-63 64.5 6.4 34 48-87 2.94 <0.001
go-cm left 59.8 4.4 25 50-66 63.9 4.7 34 54-74 3.36 57 0.001
*Test C- Cochran- Cox’ test; **Test z- U Mann- Whitney test
Table 5. Bilateral features in males and females (those with significant differences only in population from the Gródek upon the Bug River
Features Right side X̅ SD N Left side X̅ N Test t Df p
MALES
gn-go 83.4 6.5 40 85.2 5.8 40 2.48 0.0131
MaxMH 27.8 2.9 52 27.3 2.8 54 2.00 0.0461
MID 12.8 2.2 45 13.3 2.2 38 2.63 29 0.0132
FMeB 4.0 1.0 59 3.8 1.0 58 1.97 87 0.0262
FEMALES
gn-go 82.1 6.4 17 79.8 6.0 28 2.22 25 0.0261
MinMH 20.9 2.3 28 21.6 2.1 31 2.17 25 0.0402
MA 137.5 6.5 17 136.5 7.2 29 2.13 25 0.0301
go-cm 61.4 4.2 16 62.2 4.2 25 2.09 25 0.0371
1- Wilcoxon’ test; 2- Student t-test

When mandibular features were compared, a high correlation was also found between mandibular canal length (mb-ml) and mandibular foramen breath (FMaB) for males in population from Gródek upon the Bug River and Sypniewo. High correlation was also found between mandibular foramen breath (FMaB) and mental foramen breadth in males from the Sypniewo. A weak correlation was found between FMaB and FMeB for males from the Gródek upon the Bug River and for females from both populations for mental canal length and FMaB. No statistically significant correlation was found between mandibular canal length and FMeB in both populations (Tab. 6).

Table 6. Spearman’s and Person’s correlation coefficients for mandibular features in populations from Sypniewo and Gródek upon the Bug River
Cecha MALES FEMALES
mb-ml FMeB mb-ml FMeB
GRÓDEK UPPON BUG RIVER
mb-ml ­­­­­__ rs=0,01 ­­­­­­­­­__ rs=0,21
FMaB rs=0,57* r=0,32* rs=0,36* r=0,23
SYPNIEWO
mb-ml ­­­­­___ rs=0,21 ___ rs=-0,09
FMaB rs=0,50* rs=0,55* rs=0,37* rs=0,24
rs - Spearman’s correlation coefficient; r- Pearson’s correlation coefficient; * p≤0,05

For male individuals from the Grodek upon the Bug River population statistically significant weak or moderate correlation was observed between mb-ml measurement and: go-go, pg-gn, id-gn, gn-go, MinMB, MaxMB and MID and for FMaB with kdl-kr and MA as well. In addition, a high correlation (0.6) was observed between FMaB and go-go (Tab. 6). For females, statistically significant and moderate correlation was found between mb-ml and MAxMB as well as between mb-bl and pg-FMaB and between FMaB and go-gndl-kr, MinMB and go-cm. High correlation (0.5) was fount between FMaB and MA measurements (Tab. 7 and 8). For males from a population from Sypniewo average correlation was found between mb-bl and kdl-kr. High correlation was also found between mb-bl and MID. For females, mb-ml was moderately correlated with gn-go and CHM2 (Tab. 7 and 8).

Table 7. Spearman’s and Person’s correlation coefficients for unpaired mandibular features in populations from Sypniewo and Gródek upon the Bug River
Feature go-go pg-gn id-gn id-pg kdl-kdl kr-kr
GRODEK UPON BUG MALES
mb-ml rs=0.19* rs=0.41* rs=0.30* r=0.02 r=0.17 r=0.07
FMaB rs=0.06 rs =-0.03 rs =0.01 rs =0.01 rs =0.05 rs =-0.11
FMeB r=0.6* r=0.11 r=0.22 rs =-0.01 r=0.43 rs =0.16
FEMALES
mb-ml rs=0.23 rs=-0.16 rs=-0.26 rs=0.04 rs=-0.26 rs=0.27
FMaB r=0.08 r=0.01 r=-0.36 r=-0.14 r=0.35 rs=0.29
FMeB r=0.16 r=0.27 r=0.41 rs=0.18 r=0.45 rs=0.24
SYPNIEWO MALES
mb-ml rs=0.08 rs=-0.16 rs=0.02 rs=0.001 rs=-0.24 rs=-0.18
FMaB r=0.39 rs=-0.10 r=-0.26 r=-0.29 r=0.36 r=-0.04
FMeB rs=0.3 rs=-0.02 rs=-0.25 rs=-0.23 rs=0.33 rs=0.38
FEMALES
mb-ml rs=0.31 rs=0.19 rs=-0.13 rs=-0.11 rs=-0.03 rs=0.07
FMaB rs=-0.12 rs=0.11 rs=-0.22 rs=-0.20 rs=-0.28 rs=0.09
FMeB rs=-0.04 rs=0.02 r=-0.08 r=-0.17 rs=0.30 rs=0.20
rs - Spearmana correlation coefficient; r- Pearsona correlation coefficient; * p≤0,05
Table 8. Spearman’s and Person’s correlation coefficients for paired mandibular features in populations from Sypniewo and Gródek upon the Bug River
Feature gn-go pg-FMaB CHM2 MinCH MaxCH kdl-kr MID MA MinMB MaxMB go-cm
GRODEK UPON BUG MALES
mb-ml rs=0.37* rs =0.21 rs =0.02 rs =0.03 rs =0.11 rs =0.58* rs =0.37* rs =0.18 rs =0.48* rs =0.48* rs =0.23
FMaB rs =0.27 rs =-0.01 rs =0.01 rs =-0.02 rs =0.03 rs =0.47* rs =0.22 rs =0.28* rs =0.16 rs =0.21 rs =0.23
FMeB rs =0.17 rs =0.18 rs =-0.01 rs =0.17 rs =0.22 rs =-0.03 rs =0.33 rs =0.23 rs =-0.07 rs =-0.001 rs =0.07
FEMALES
mb-ml rs=-0.14 rs=0.45* rs=0.24 rs=0.22 rs=0.25 rs=0.18 rs=0.10 rs=-0.01 rs=0.28 rs=0.36* rs=-0.01
FMaB rs=0.35* rs=0.34 rs=0.12 rs=0.31 rs=0.32 rs=0.36* rs=0.33 rs=0.50* rs=0.45* rs=0.12 rs=0.47*
FMeB rs=0.06 rs=0.28 rs=0.21 rs=0.20 rs=0.30 rs=0.10 rs=0.18 rs=0.06 rs=0.18 rs=0.04 rs=0.10
SYPNIEWO MALES
mb-ml rs=0.24 rs=-0.21 rs=0.32 rs=0.17 rs=0.08 rs=0.46* rs=0.53* rs=0.24 rs=0.21 rs=0.25 rs=0.35
FMaB rs=0.33 r=-0.45 r=0.13 r=-0.20 r=-0.20 rs=0.17 r=0.02 rs=0.48* r=-0.46 rs=-0.15 rs=0.22
FMeB rs=0.01 rs=-0.25 rs=-0.26 rs=-0.32 rs=-0.33 rs=-0.17 rs=0.13 rs=0.004 rs=0.10 rs=-0.02 rs=-0.12
FEMALES
mb-ml rs=0.41* rs=-0.02 rs=0.34* rs=0.21 rs=0.16 rs=0.24 rs=0.06 rs=0.11 rs=0.15 rs=0.11 rs=0.35
FMaB rs=0.22 rs=-0.26 rs=0.28 rs=0.15 rs=0.17 rs=0.13 rs=-0.004 rs=-0.11 rs=-0.07 rs=0.16 rs=0.16
FMeB rs=-0.13 rs=-0.14 rs=-0.07 rs=-0.15 rs=-0.10 rs=-0.10 rs=0.04 rs=-0.45* rs=-0.13 rs=0.08 rs=-0.27

Discussion

Occurrence of the mental foramen is relatively constant, however, the location is variable. Thus, each individual may exhibit a different arrangement of the neurovascular bundle exit. The position and the direction of the exit of the neurovascular bundle were similar to other European populations (Tab. 9, 10). However, differences in localization between the two investigated populations were observed. Thus, it could suggest that not only genetic but also environmental (geographical) factors, such as living conditions (e.g., diet, which may affect developmental stability), may influence the morphology of the mandibular features.

The literature review revealed a broad variety of features characterized by the human mandible (Tab. 9) which may result from both different environmental conditions (e.g., different food accessibility) as well as nutrition culture. In poorer populations, for instance, a scarcity of food may result in the incorrect realization of the bone growth path. Moreover, nutrition culture, such as consistency and type of food, may result in differences in chewing intensity and, therefore, different sizes of the mandible (Raadsheer et al. 1999; Golusik et al. 2005). A secular trend observed in populations from different time ranges is also an important factor influencing the mandible’s features.

Table 9. Comparison of studies concerning the morphometry of the mandibular features according to sexes [in mm]
Author, year of publication N Population, time ranges Sex Features (mean± SD)
go-go id-gn gn-go kdl-kdl MA go-cm
This study, 2020 50
25
Poland (Sypniewo), XI-XIIth Female
Male
94.1±7.4
98.2±6.3
23.1±2.9
26.1±3.9
77.6±3.8
81.2±4.7
115.2±3.8
121.9±4.7
138.2±5.3
138.5±6.1
58.2±3.7
64.6±4.3
75 TOTAL 95.8±7.1 24.0±3.5 79.1V4.5 117.7±5.2
This study, 2020 34
60
Poland (Gródek upon Bug), XIII-XVIth Female
Male
98.2±5.5
101.9±8.2
23.8±2.4
26.2±3.4
80.7±6.4
82.2±7.4
116.3±4.3
122.3±6.5
136.2±6.8
134.8±6.8
59.6±4.0
64.6±6.0
94 TOTAL 100.5±7.4 25.3±3.3 81.7±7.0 119.7±6.3
Mays, 2014 15
17
Nederland, XIXth Female
Male
91.1±7.5
99.9±6.8
69.7±.3.3
76.3±7.6
113.1±6.3
116.9±6.9
134.0±8.3
126.9±8.7
15
17
England, X-XIXth Female
Male
96.2±7.1
105.1±7.1
70.5±6.1
76.2±4.7
116.7±7.7
124.2±5.7
126.4±6.4
122.6±9.0
Purmal et al., 2013 46
44
Malaisia, XXth Female
Male
103.9±5.4
106.7±7.8
34 TOTAL 105.2±6.7
China, XXth Female
Male
105.3±6.5
108.2±7.5
30 TOTAL 106.7±7.1
India, XXth Female
Male
98.7±8.4
111.1±10.0
26 TOTAL 104.9±11.0
Simalcsik et al., 2012 299
259
Romania,XVI-XVIIIth Female
Male
94.1±7.3
104.8±9.0
28.6±3.0
32.4±3.0
66.1±5.1
69.1±4.8
112.8±7.2
123.9±8.4
60.2±4.8
64.9±5.0
Ongkana et al., 2009 102 Thailand, XXth Female
Male
28.2±6.5
28.3±6.1
79.2±4.6
83.2±5.2
116.1±5.9
123.8±6.3
62.6±5.6
68.1±4.4
Golusik et al. 2005 16
69
Poland (Złota), II-IIIth BC Female
Male
94.1±4.6
99.9±8.4
30.4±5.0
34.1±3.1
80.0±3.8
84.6±4.5
113.9±5.6
118.2±6.9
85 TOTAL 97.00 32.0 82.5 116.0
24
22
Poland (Milicz), XII-XIIIth Female
Male
93.4±4.9
100.3±7.5
30.9±2.2
31.8±3.3
83.4±5.1
86.1±7.0
112.8±8.3
118.5±7.7
47 TOTAL 97.0 31.5 84.5 115.5
104
160
Poland (Gródek upon Bug), XIII-XVIIth Female
Male
94.6±6.4
101.5±7.3
27.0±2.7
30.3±3.0
77.0±4.8
81.2±4.8
116.2±6.0
121.7±7.1
264 TOTAL 98.0 28.5 79.0 119.0
28
70
Poland (Warsaw), XXth Female
Male
94.6±6.6
98.0±7.7
27.5±3.2
30.3±3.4
77.0±4.3
83.0±5.0
110.1±6.6
116.3±6.1
98 TOTAL 96.5 29.0 80.0 114.0
Fabian and Mpembeni, 2002 25
25
Tanzania Bantu, ?? Female
Male
77.0±3.9
80.6±3.8
Puisorua et al., 2006 91 Europe, Near East, Asia, Africa, ?? Female
Male
91.0±3.61
114.1±38.91
Female
Male
89.0±1.82110.0±3.62
Female
Male
95.0±1.673119.0±29.93
Zimbabwe, ?? Female
Male
91.0±3.6
114.0±38.9
128.0
123.0
Nigeria, ?? Female
Male
TOTAL 118.8
Turkey, ?? Female
Male
TOTAL 120.2
USA, ?? Female
Male
126.5
127.8
Spain, ?? Female
Male
TOTAL 118.1
China, ?? Female
Male
TOTAL 121.2
Romania, ?? Female
Male
125.0±1.2
119.0±1.1
Legend: ??- data unavailable, 1- full dentition; 2- uncomplete dentition; 3- no dentition

In this study, differences between sexes were found in both analyzed populations. However, for the population from Sypniewo (which is considered as rural population), we found fewer features that exhibited significant sex differences. When the sex of the individuals was controlled for the population from Gródek upon the Bug River, sexual dimorphism was observed in even more features and was slightly higher (7.5%) (Tab. 3 and 4). When sexual dimorphism was lower, living conditions, and thus, socioeconomic status of the population, are considered worse. Sexual dimorphism of the human body is well established. It may be the result of the environmental factors and lifestyle; sexual dimorphism may also be the result of genetic factors (Galdames et al. 2008; Mays 2014). Moreover, disorders of the endocrine system may also result in sex differences in the morphology of the human mandible (Piontek 1999) and greater masticatory forces may result in sexual dimorphism of the mandible. In general, there is less sexual dimorphism in body size in populations with poorer socio-economic status and living in unfavorable environmental conditions (Wells 2012; Tomaszewska et al. 2015). This conclusion may be also related to diet and eating habits. Our results support previous studies, which contend that worse environmental conditions may influence cranial morphology and, ultimately, disrupt an individual’s skeletal development (Gilligan and Bulbeck 2007; Harvati and Weaver 2006; Pearson 2000; Perez et al. 2007; Wells 2012).

Table 10. Comparison of studies concerning the morphometry of the mandibular features according to body side [in mm]
Author, year of publication N Population, time ranges Body side Feature
go-cm MA FMeB FMaB Mb-ml
This study, 2020 75 Poland (Sypniewo), XI-XIIth Right
Left
61.5±4.9
60.6±5.2
138.3±5.7
138.3±5.8
3.5±1.3
3.3±1.3
2.7±0.7
2.6±0.8
56.4±3.6
56.8±3.9
This study, 2020 94 Poland (Gródek upon Bug), XIII-XVIth Right
Left
62.8±6.1
62.1±5.0
135.0±7.7
135.9±7.1
3.9±0.9
3.8±1.0
3.7±3.1
3.4±0.9
58.8±4.3
59.2±4.4
Shenoy et al., 2012 50 India, ?? Right
Left
124.4±6.0
124.1±6.2
Ennes and Monteiro de Medeiros, 2009 99 Brazil, ?? Right
Left
131.8±8.51
131.2±8.21
Right
Left
125.6±7.82
125.7±9.22
Right
Left
126.5±7.83
125.7±9.23
Prośba-Mackie­wicz et al., 2005 40 Poland, ?? Right
Left
64.0±4.84
63.5±4.84
Oguz and Bozkir, 20027 34 Turkey, ?? Right
Left
65.6±5.0
64.6±4.2
120.2±4.7
120.2±3.6
Rai et al., 2014 40 India, ?? Right
Left
2.6±0.9
2.6±0.9
Hoque et al., 2013 185 Bangladesh, ?? Right
Left
2.6±0.7
2.5±0.5
Agarwal and Gupta, 2011 100 India, ?? Right
Left
3.3
3.3
Junior et al., 2010 50 Brasil, XXth Right
Left
52.8
51.6
Singh and Srivastar, 2010 100 Turkey, ?? Right
Left
2.8
2.6
Ilayperuma et al., 2009 51 Sri Lanka, ?? Right
Left
3.3±0.9
3.4±0.8
Oliveira Junior et al., 2009 80 Brasil, ?? Right
Left
2.4±0.6
2.4±0.6
Wychowański et al., 2008. 100 contemporary Right
Left
3.7±1.0
3.8±1.0
3.2±0.6
3.4±0.6
Right
Left
3.3±0.7
3.8±1.1
3.5±0.5
3.3±0.4
Igbigbi and Lebona, 2005 70 Malawi-
??
Right
Left
2.4±0.2
2.7±0.2
Prośba-Mackiewicz et al., 2005 40 ?? Right
Left
2.7±1.01
2.8±1.01
3.9±0.91
4.0±0.91
Right
Left
2.9±1.14
2.8±1.04
4.1±1.82
4.2±1.72
Goudot, 2002 1 France* - paleolith Right
Left
4.5
4.5
Goudot, 1999 1 France*- 60000- 45000 Right
Left
6.0
6.0
5.0
5.0
Phillips et al., 1992 75 ?? Right+ Left 2.9
Legend: 1 – no dentition; 2 mandibles with 1 to 10 teeth; 3 mandibles with 11 to 16 teeth; 4 partial lack of dentition; * Neanderthal’s mandible.

Foraminal area of the mandible is considered as an important region relevant to anatomy, surgery, anthropology and forensic medicine. The position of the mental and mandibular foramina has been reported to vary in populations from different geographical regions. Currently, to our knowledge, there have not been any investigations concerning the position and morphology of these foramina in populations with divergent socio-economic statuses (SES). The SES may influence lifestyle and some behavioral habits regarding food consumption, consumed food type as well as breastfeeding. Developmental stability may also influence dental eruption, and this may possibly influence the position of the mental foramen. Positional change of mental foramen is a combination of osseous growth in the region combined with a mesial drift of the dental anlage. Williams and Krovitz (2004) stated that the mental foramen migrates posteriorly during ontogeny and found that the mental foramen forms prenatally under the anticipated anterior root of the developing first deciduous molar. Williams and Krovitz (2004) also asserted that this position is maintained at birth and remains mostly stable during the deciduous eruption. During the eruption of the second molar, the mental foramen generally migrates to a position inferior to the second premolar (Hasan 2012; Narayana and Prashanthi 2003).

Possible limitations of this study may result from the anatomical variation in the mandibular area especially given that we did not analyze additional/ accessory mandibular and mental foramina in order to show only variation in mental/mandibular foramina and mandibular canal. If a large accessory mental foramen exists, that could make a regular mental foramen smaller than the foramen on contralateral side (if the contralateral side does not have the accessory mental foramen) (Iwanga et al. 2016). We are also aware that in cone- beam computed tomography different aspects of mandibular canal may occur (i.e. bifid or trifid mandibular canal (Naitoh et al. 2007). Bifid mandibular canal exhibits a variety of incidence, ranging from 0,08 to 65% (Mizbah et al. 2012; Miličević et al. 2021), which may not be seen in panoramic or periapical films (Dario 2002). Its occurrence depends on the assessment method (cone-beam computed tomography or panoramic radiographs) but for anthropological and archaeological field works purposes only macroscopic assessment is useable. Hence, this research is based on macroscopic observations and dedicated for field works/ excavations macroscopic examinations, where sophisticated methods are not possible to conduct. As such, this study aimed to facilitate conclusions based on macroscopic observations although for clinical studies this method could not be sufficient. Nevertheless, the results of our study should be considered when sudden and unplanned interventions in this region are conducted.

Conclusion

The results derived from different studies (please see Tab. 9 and 10 for details) may be flawed due to the application of different methods (Hasan 2012). In addition, the observed differences between right and left sides of the mandible may result from chewing habits (unilateral) (Sójka, Hędzelek 2011). Literature reviews revealed that although studies on the morphology and morphometry of mental and mandible foramina are common, research specifically focused on the distances between these foramina and morphology of the mandible canal are rather rare (Tab. 10). In this study we argue that such (methodological) differences should be considered when approaching to the mandibular canal during anesthetic, surgical and forensic procedures.


Conflict of interests
The authors declared no conflicts of interests


Authors’ contribution
JR collected the data and performed statisti­cal computations.
DP was project supervisor, co- edited the final version of the manuscript.
AT conceived the paper, performed statistical computations, drafted the manuscript and co- edited the final version of the manuscript.
All authors carefully read and accepted the final version of the manuscript.


* Corresponding author: Agnieszka Tomaszewska, Department of Anthropology, Wroclaw University of Environmental and Life Sciences, Poland; e-mail: agnieszka.tomaszewska@upwr.edu.pl


Financial support: This work was supported by the Wrocław University of Environmental and Life Sciences (Poland) as the Ph.D. research program “Innowacyjny Naukowiec”, no. N060/0005/21.



References

Agarwal DR, Gupta SB. 2011. Morphometric Analysis of Mental Foramen in Human Mandibles of South Gujarat. People’s Journal of Scientific Research 4(1):15–18.

Belniak T, Krupiński T, Magnuszewicz M, Rauhut J, Szczotkowa Z. 1961. Cmentarzysko w Gródku nad Bugiem (XIII–XVII w.). Mat. Pr. Antrop. 50.

Bierman F. 2006. Sypniewo. Ein fruhmittelalterlicher Burg-Siedlungskomplex in Nordmasowien. Befunde, funde und kulturhistorische bewertung, teil 1. Archeologia Mazowsza i Podlasia. Studia i materiały. T. 4. Red. serii: W. Szymański. Instytut Archeologii i Etnologii PAN, Warszawa.

Cutright B, Quillopa N, Schubert W. 2003. An anthropometric analysis of the key foramina for maxillofacial surgery. Journal of Oral and Maxillofacial Surgery 61(3):354–357.

Dario LJ. 2002. Implant placement above a bifurcated man-dibular canal: A case report. Implant. Dent. 11:258–261.

Drake RL, Vogl AW, Mitchell AWM. 2010. Gray’s Anatomy for Students. Churchill Livingstone 1142–1144.

Ennes JP, Monteiro de Medeiros R. 2009. Localization of Mandibular Foramen and Clinical Implications. Int. J. Morphol. 27(4):1305–1311.

Fabian FM, Mpembeni R. 2002. Sexual dimorphism in the mandibles of homogenius black population of Tanzania. Tanzania Journal of Science. 28(2):47–54.

Field A. 2006. Discovering statistics using SPSS. 3rd edition, Sage Publications Ltd., London.

Galdames ICS, Matamala DAZ, Smith RL. 2008. Evaluating Accuracy and Precision in Morphologic Traits for Sexual Dimorphism in Malnutrition Human Skull: a Comparative Study. Int. J. Morphol. 26(4): 877–881.

Gilligan I, Bulbeck D. 2007. Environment and morphology in Australian Aborigines: a re – analysis of the Birdsell database. Am. J. Phys. Anthropol. 134:75–91.

Golusik K, Sarul M, Rzeszut Ł, Matthews­-Brzozowska T. 2005. Żuchwa ludzka w procesie ewolucji. Dent. Med. Probl. 42(1):103–109.

Goudot P. 1999. The mandibular canal of a Neanderthal: the La Chapelle-aux-Saints man anatomical-radiological study. J. Craniomaxillofac Surg. 27:134–139.

Goudot P. 2002. The mandibular canal of the “Old Man” of Cro-Magnon: anatomical-radiological study. J. Craniomaxillofac Surg. 30:213–218.

Gray H. 1985. Anatomy of the Human Body. Philadelphia : Lea & Febiger, United States 106–109.

Green RM. 1987. The position of the mental foramen: a comparison between the southern (Hong Kong) Chinese and other ethnic and racial groups. Oral. Surg. Oral Med. Oral Pathol. 63:281–290.

Harvati K, Weaver TD. 2006. Human cranial anatomy and the differential preservation of population history and climate signatures. Anat. Rec., Part A Discov. Mol. Cell. Evol. Biol. 288 A (12):1225–1233.

Hasan T. 2012. Mental Foramen Morphology: a must know in clinical dentistry. Journal of the Pakistan Dental Association 21(3):168–173.

Hoque M, Ara S, Begum S, Kamal M, Momen M. 2013. Study of Number, Shape, Size and Position of Mental Foramen in Bangladeshi Dry Adult Human Mandible. Bangladesh Journal of Anatomy 11(1):7–10.

Igbigbi PS, Lebona S. 2005. The position and dimensions of the mental foramen in adult Malawian mandibles. WAJM 24(3):184–189.

Ilayperuma I, Nanayakkara G, Palahepitiya N. 2009. Morphometric Analysis of the Mental Foramen in Adult Sri Lankan Mandibles. International Journal of Morphology 27(4):1019–1024.

Iwanaga J, Watanabe K, Saga T, Tabira Y, Kitashima S, Kusukawa J, Yamaki K. 2016. Accessory mental foramina and nerves: Application to periodontal, periapical, and implant surgery. Clinical Anatomy 29(4):493–501. https://doi.org/10.1002/ca.22635

Jacobs R, Mraiwa N, Van Steenberghe D, Sanderink G, Quirynen M. 2004. Appearance of the mandibular incisivecanal on panoramic radiographs. Surg Radiol Anat 26:329–333.

Junior ROM, Santos Saud AD, Rodrigues Fonseca D, De-Ary-Pires B, Ary Pires-Neto M, De Ary-Pires R. 2010. Morphometrical analysis of the human mandibular canal: a CT investigation. Surgical and Radiologic Anatomy 33:345–352.

Łasiński W. 1993. Anatomia głowy dla stomatologów. Państwowy Zakład Wydawnictw Lekarskich, Warszawa 26–30.

Martin R, Saller F, Knussman R. 1988. Antropologie In: Handbuch der vergleichenden Biologie des Menschen, Gustav Fischer Verlag, Stuttgart, New York.

Mays S. 2014. Mandibular morphology in two archaeologicalhuman skeletal samples from northwest Europewith different masticatory regimes. HOMO – Journal of Comparative Human Biology 25378:1–13.

Miličević A, Salarić I, Đanić P, Miličević H, Macan K, Orihovac Ž, Zajc I, Brajdić D, Macan D. 2021. Anatomical Variations of the Bifid Mandibular Canal on Panoramic Radiographs in Citizens from Zagreb, Croatia. Acta Stomatologica Croatica 55(3):248–255. https://doi.org/10.15644/asc55/3/2

Mizbah K, Gerlach N, Maal TJ, Bergé SJ, Meijer GJ. 2012. The clinical relevance of bifid and trifid mandibular canals. Oral Maxillofacial Surgery 16(1):147–151. https://doi.org/10.1007/s10006-011-0278-5

Moiseiwitsch JRD, Hill C. 1998. Position of the mental foramen in a North American, white population. Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology 1, 85:457–460.

Naitoh M, Hiraiwa Y, Aimiya H, Ariji E. 2009. Observation of bifid mandibular canal using cone-beam computerized tomography. International J Journal of Oral and Maxillofacial Implants 24:155–159.

Narayana K, Prashanthi N. 2003. Incidence of large accessory mandibular foramen in human mandibles. European Journal of Anatomy 7(3):139–141.

Oguz O, Bozkir MG. 2002. Evaluation of Location of Mandibular and Mental Foramina in Dry, Young, Adult Human. West Indian Medical Journal 51(1):14–16.

Oliveira Junior EM, Araújo ALD, Da Silva CMF, Sousa-Rodrigues CF, Lima FJC. 2009. Morphological and Morphometric Study of the Mental Foramen on the M-CP-18 Jiachenjiang Point. International Journal of Morphology 27(1):231–238, https://doi.org/10.4067/S0717-95022009000100039

Ongkana N, Sudwan P. 2009. Gender difference in Thai mandibles using metric analysis. Chiang Mai,Medical Journal 48(2):43–48.

Pearson OM. 2000. Activity, climate, and postcranial robusticity: implications for modern human origins and scenarios of adaptive change. Current Anthropology 41(4):569–607.

Perez SI, Bernal V, Gonzalez PN. 2007. Morphological differentiation of aboriginal human populations from Tierra del Fuego (Patagonia): implications for South American peopling. American Journal of Physical Anthropology 133:1067–1079.

Phillips JL,Weller RN, Kulild JC. 1992. The Mental Foramen: Part III. Size and Position on Panoramic Radiographs. Journal of Endodontics 18(8):383–386.

Piontek J. 1999. Biologia populacji pradziejowych. Wydawnictwo Naukowe Uniwersytetu im. Adama Mickiewicza w Poznaniu, Poznań.

Prośba-Mackiewicz M, Mackiewicz J, Grzybiak M, Hreczecha J, Skwarek M. 2005. Zastosowanie badań morfometrycznych do oceny ważnych klinicznie parametrów morfologicznych żuchwy. Czasopismo Stomatologiczne LVIII, 2:116–123.

Puisorua M, Fornab N, Fatub AM, Fatub R, Fatua C. 2006. Analysis of mandibular variability in humans of different geographic areas. Annals of Anatomy 188:547–554.

Purmal K, Alam MK, Moganadass D, Zakariat NN, Cheong NW. 2013. The application and correlation of Pont’s Index to the facial framework of three main ethnic groups in Malaysia. Australian Orthodontic Journal Volume 29(1): 34–42.

Raadsheer MC, Van Eijdet TMGJ, Van Ginkel FC, Prahl-Andersen B. 1999. Contribution of jaw muscle size and craniofacial morphology to human bite force magnitude. Journal of Dental Research 78:31–42.

Rai R, Shrestha S, Jha S. 2014. Mental foramen: a morphological and morphometrical study. International Journal of Healthcare and Biomedical Research 2(4):144–150.

Renton T, Adey-Viscuso D, Meechan J. et al. 2010. Trigeminal nerve injuries in relation to the local anaesthesia in mandibular injections. British Dental Journal 209, E15 https://doi.org/10.1038/sj.bdj.2010.978

Samanta PP, Kharb P. 2013. Morphometric analysis of mandibular foramen and incidence of accessory mandibular foramina in adult human mandibles of an Indian Population. Revista Argentina de Anatomia 5(2):60–66.

Sekutowski M. 2002. Wybrane cechy niemetryczne kości kończyny dolnej a przypuszczalny tryb życia średniowiecznych populacji z Sypniewa i Wrocławia (praca magisterska obroniona w Katedra Antropologii. Wrocław: Uniwersytet Wrocławski).

Shenoy V, Vijayalakshmi S, Saraswathi P. 2012. Osteometric Analysis of the Mandibular Foramen in Dry Human Mandibles. Journal of Clinical and Diagnostic Research 6(4):557–560.

Simalcsik A, Groza VM, Simalcsik RD, Miu G. 2012. The Medieval Nectropolis (16th–18th centuries) of ‘Sfantul Nicolae-Ciurchi’ Church from Iasi city (Romania): Anthropologic data. Biologie animală LVIII:183–194.

Singh R, Srivastav AK. 2011. Evaluation of position, shape, size and incidence of mental foramen and accessory mental foramen in Indian adult human skulls. Int. J. Experim. Clinical Anat. 5:23–29.

Sójka A, Hędzelek W, 2011. Ocena różnych rodzajów asymetrii w narządzie żucia na podstawie badania klinicznego i instrumentalnego. Protet. Stomatol. LXI(1):28–36.

Sonick M, Abrahams J, Faiella R. 1994. A comparison of the accuracy of periapical, panoramic, and computerized tomographic radiographs in locating the mandibular canal. Int. J. Oral. Maxillofac. Implants. 9:455–460.

Stanisz A. 1998. Przystępny kurs statystyki w oparciu o program STATISTICA PL na przykładach z medycyny. Kraków: StatSoft Polska.

Tomaszewska A, Kwiatkowska B, Jankauskas R. 2015. Is the area of the orbital opening in humans related to climate? Am. J. Hum. Biol. 27(6):845–850. https://doi.org/10.1002/ajhb.22735. Epub 2015 May 7.

Valente VB, Arita WM, Gonçalves PCG, Campos JADB, de Oliveira Capot TS. 2012. Location of the Mandibular Foramen According to the Amount of Dental Alveoli. Int. J. Morphol. 30(1):77–81.

Wells JCK. 2012. Sexual dimorphism in body composition across human populations: associations with climate and proxies for short – and long – term energy supply. Am. J. Hum. Biol. 24(4):411–419.

Wiliams FL, Krovitz GE. 2004. Ontogenetic migration of the mental foramen in Neandertals and modern humans. J. Hum. Evol. 47(4):199–219.

Workshop of European Anthropologists. 1980. Recommendations for sex and age diagnoses of skeletons. J. Hum. Evol. 9:517–549.

Wychowański P, Nieckula P, Panek M, Kalinowski E, Borkowska U, Wojtowicz A. 2008. Próba oceny położenia otworu żuchwowego i bródkowego na podstawie analizy cyfrowych zdjęć pantomograficznych. Dent Med. Probl. 45(1):21–28.

Yosue T, Brooks SL. 1989. The appearance of mental foramina on panoramic and periapical radiographs. II. Experimental evaluation. Oral Surg Oral Med Oral Pathol. 68(4):488–492. https://doi.org/10.1016/0030-4220(89)90151-5



COPE
CC

Received: 2021-09-23. Revised: 2022-05-11. Accepted: 2022-05-18