Professional Documents
Culture Documents
Introduction: The purpose of this study was to assess the growth of the cranial base in a sample of patients
diagnosed with Down syndrome (DS). Methods: The sample comprised 47 subjects (25 boys, 22 girls) with
DS. All patients had at least 2 x-rays that showed the cranial base. To make comparisons among age groups,
the sample was divided into 3 groups: prepubescent (8-11 years), pubescent (12-14 years), and postpubes-
cent (15-18 years). A control group included 38 normal subjects (22 boys, 16 girls, without DS) who were part
of a longitudinal growth sample. Computerized cephalometric analysis was performed on all subjects, and
cephalometric superimpositions were made. Two-way ANOVA was used to study the overall changes
between groups. In addition, 1-way ANOVA and the Duncan multiple range test were used to analyze
possible differences in the age groups. Results: Cranial base growth in patients with DS from age 8 to 18 was
similar to that of the control group. Structural differences in the cranial base are established before 8 years
of age and consist of shorter, flatter anterior and posterior bases. (Am J Orthod Dentofacial Orthop 2008;133:
729-37)
own syndrome (DS), described by Down1 in sinus.8 The ethmoid bone is retruded, thereby forming
Table I. Cephalometric superimposition variables and cephalometric variables: comparison of the 2 groups (Student
t test)
Postpubescent (15-18
Cranial base parameters Total (8-18 y) Prepubescent (8-11 y) Pubescent (12-14 y) years)
Variable Unit Group Average SD Sig Average SD Sig Average SD Sig Ave. SD Stat. Sig.
Horiz N (mm/y) D 0.47 0.49 0.49 0.37 P 0.01 0.69 0.60 NS 0.25 0.33 P 0.01
C 0.75 0.41 0.77 0.42 0.73 0.42 0.76 0.29
Vert N (mm/y) D 0.13 0.15 0.18 0.18 NS 0.17 0.14 NS 0.05 0.11 P 0.05
C 0.14 0.07 0.14 0.06 0.14 0.08 0.15 0.06
Horiz Ba (mm/y) D 0.48 0.53 0.77 0.62 P 0.01 0.55 0.50 NS 0.21 0.33 P 0.05
C 0.40 0.45 0.32 0.40 0.48 0.52 0.49 0.24
Vert Ba (mm/y) D 0.36 0.45 NS 0.60 0.56 NS 0.41 0.46 NS 0.16 0.23 NS
C 0.40 0.47 0.47 0.46 0.32 0.50 0.25 0.22
Basal (/y) D 0.49 1.19 0.74 1.36 P 0.01 0.38 1.20 NS 0.42 1.05 NS
angle C 0.15 0.70 0.06 0.66 0.39 0.71 0.47 0.26
SN (mm) D 63.77 4.04 P 0.001 61.85 3.68 P 0.001 63.99 3.91 P 0.001 64.81 3.98 P 0.001
C 72.26 2.84 71.15 2.66 73.02 2.80 73.83 2.00
CCN (mm) D 52.42 3.19 P 0.001 50.59 2.96 P 0.001 52.62 3.11 P 0.001 53.42 2.91 P 0.001
C 60.23 3.00 58.97 3.06 61.04 2.59 62.23 2.06
SBa (mm) D 42.33 3.22 P 0.001 39.94 2.91 P 0.001 43.04 3.00 P 0.001 43.31 2.81 P 0.001
C 46.30 3.03 45.53 2.78 46.78 3.13 47.52 3.02
NBa (mm) D 100.90 5.55 P 0.001 96.98 4.26 P 0.001 101.50 5.49 P 0.001 102.90 5.10 P 0.001
C 109.60 4.36 107.90 4.40 110.60 3.81 112.90 3.00
SNBa () D 143.40 4.76 P 0.001 143.30 5.37 P 0.001 142.60 4.06 P 0.001 144.00 4.83 P 0.001
C 133.90 4.12 133.90 3.95 133.50 4.19 135.60 4.31
Deflection () D 27.12 2.26 P 0.001 27.48 2.92 P 0.001 26.92 2.08 P 0.001 27.05 1.87 P 0.05
C 29.01 1.84 29.25 1.76 28.93 1.94 28.35 1.70
CCPo (mm) D 43.37 3.84 NS 42.42 4.33 NS 43.61 3.57 NS 43.80 3.66 NS
C 43.27 2.47 42.72 2.63 43.75 2.29 43.69 2.06
D, Down syndrome group; C, control group; Sig, statistical significance; NS, not significant.
cordance type III, a greater difference than previously plied the least square means correction to find differ-
described. ences in the data of the arithmetic means.
In concordance type II, the arithmetic mean be- Because the samples were unequal, we could only
tween the 2 values is established for the parameter that compare the overall averages when the ANOVA with
does not coincide. When the difference is greater interaction did not find statistical significance. Other-
(concordance type III), the lines are drawn, and the wise, it is methodologically more appropriate to estab-
measurements are made again, bearing in mind the 3 lish the comparison according to age groups, thereby
types of concordance. Standard error was determined avoiding doing so with overall averages. When we
with the Dahlberg formula (SE 76d2/2n),30,31 and were able to compare overall averages (nonsignificant
the systematic error was found by using the Student t ANOVA), we did so using the least square means
test at P 0.05.32-34 A descriptive statistical analysis correction because it is more precise than the Student t
was carried out to evaluate the data obtained in which test when assigning statistical significance.
we included the arithmetic mean, percentage, and range In each group and to compare the different age
(maximum and minimum values) of each variable for groups, we applied 1-way ANOVA followed by the
each group (DS and control) according to sex and age. Duncan multiple range test as an a posteriori test with
Then an analytical or inferential statistical analysis was a 0.05 confidence level. To determine the differences
done in which the differences between the 2 groups between the sexes, we also used the Student t test.
were analyzed by using the Student t test for indepen-
dent samples to establish comparisons between age RESULTS
groups. To study the evolution of each variable over Table I gives average values, standard deviations,
time and to establish comparisons in the behavior of 1 and statistical significance, after the Student t test, of
particular variable in each group, we used the 2-way the values obtained from the cephalometric superimpo-
analysis of variance (ANOVA) with interaction. When sition method. The values studied were the horizontal
this test did not show significant differences, we ap- growth of N (horiz N), vertical growth of N (vert N),
732 Alio, Lorenzo, and Iglesias American Journal of Orthodontics and Dentofacial Orthopedics
May 2008
Table II. Cephalometric variables of superimposition and cephalometric variables: differences between the sexes in
the 2 groups (Student t test)
Females Males
Variable of superimposition
Horiz N (mm/y) D 0.48 0.56 0.46 0.43 NS
C 0.68 0.40 0.81 0.41 NS
Vert N (mm/y) D 0.13 0.15 0.12 0.15 NS
C 0.15 0.08 0.13 0.06 NS
Horiz Ba (mm/y) D 0.45 0.48 0.50 0.56 NS
C 0.27 0.33 0.50 0.50 P 0.01
Vert Ba (mm/y) D 0.46 0.48 0.29 0.42 NS
C 0.18 0.25 0.58 0.53 P 0.01
Basal angle (/y) D 0.55 1.37 0.22 1.05
C 0.06 0.61 0.22 0.76 NS
Cephalometric variables
SN (mm) D 61.15 2.32 65.84 3.92 P 0.001
C 71.29 2.73 73.03 2.71 P 0.001
CCN (mm) D 50.34 2.06 54.06 2.96 P 0.001
C 59.46 2.71 60.87 3.10 P 0.01
SBa (mm) D 40.37 2.68 43.88 2.75 P 0.001
C 45.36 2.45 47.04 3.26 P 0.001
NBa (mm) D 96.80 3.51 104.13 4.67 P 0.001
C 108.51 4.28 110.49 4.25 P 0.01
SNBa () D 144.14 4.75 142.76 4.71 NS
C 135.65 4.15 132.55 3.55 P 0.001
Deflection () D 27.55 2.07 26.77 2.35 P 0.05
C 29.15 2.00 28.89 1.71 NS
CCPo (mm) D 41.53 3.32 44.83 3.60 P 0.001
C 42.56 2.58 43.84 2.24 P 0.01
D, Down syndrome group; C, control group; Sig, statistical significance; NS, not significant.
horizontal growth of Ba (horiz Ba), vertical growth of cent, pubescent, and postpubescent) with the 1-way
Ba (vert Ba), and changes in the angle of the base (basal ANOVA and the a posteriori Duncan test. For the DS
angle). In the first column are the total average values group, regarding horizontal and vertical growth of N, the
for both groups. In the next 3 columns, the same values group that distinguished itself from the others was the
appear but are separated into the prepubescent, pubes- postpubescent group. The same occurred for growth of
cent, and postpubescent stages. In the lower half of Ba, even though in this case and regarding horizontal
Table I, we show these same data but here applied to growth, its behavior was different in each of the 3 age
the cephalometric variables themselves. All variables groups. To make these data easier to understand, we
show significant differences between the groups for the present the same finding in Figure 2 regarding the hori-
total sample as well as the 3 age groups. zontal growth of N. In the DS group, there was forward
Table II presents the differences between the sexes growth of N of 0.47 mm per year, whereas in the control
in the DS patients and the control group. In the group, it was 0.75 mm per year. Therefore, the growth rate
cephalometric superimposition variables, the only sta- was slower in the DS group, especially in the prepubes-
tistically significant differences appeared in the control cent and postpubescent stages (P 0.01). In the vertical
group and in the growth of Ba, both vertically and plane (Fig 3), the prepubescent DS groups vertical
horizontally. The differences between the sexes in the growth was limited (0.13 mm per year) but was similar to
cephalometric variables were significant except for the the control groups 0.18 mm per year. From the age of 15
cranial base and cranial deflection angles. onward, growth of N in the DS group slowed to a halt,
Table III, in the first column, gives the results of the vertically and horizontally, with virtually no annual
2-way ANOVA, which allowed us to analyze the evolu- growth. However, this growth limitation was not seen in
tion of the different parameters over time between both the control group, where this landmark shows regular,
groups. In the next column, each group is analyzed constant growth.
individually, comparing the 3 age subgroups (prepubes- If we look at Figures 4 and 5 and Tables I and III,
American Journal of Orthodontics and Dentofacial Orthopedics Alio, Lorenzo, and Iglesias 733
Volume 133, Number 5
Variables of superimposition
Horiz N D P0.05 NS NS P0.05
C NS NS NS
Vert N D P0.05 NS NS P0.05
C NS NS NS
Horiz Ba D P0.001 P0.05 P0.05 P0.05
C NS NS NS
Vert Ba D NS NS NS P0.05
C NS NS NS
Basal angle D P0.05 NS NS NS
C P0.05 NS NS
Cephalometric variables
SN D NS P0.05 NS NS
C P0.05 NS NS
CCN D NS P0.05 NS NS
C P0.05 NS NS
SBa D NS P0.05 NS NS
C P0.05 NS P0.05
NBa D NS P0.05 NS NS
C P0.05 P0.05 P0.05
SNBa D NS NS NS NS
C NS NS NS
Deflection D NS NS NS NS
C NS NS NS
CCPo D NS NS NS NS
C NS NS NS
we can analyze the horizontal (posterior) and vertical 2-way ANOVA (Table III) was applied, horizontal
growth of Ba. No significant differences were shown growth differences appeared between the 2 groups, but
with the Student t test. In the DS group, horizontal there were no vertical differences. In short, the evolu-
growth was 0.48 mm per year, and, in the control tion of Ba growth over time is similar to that of N,
group, it was 0.40 mm per year. Vertical growth in the slowing to a virtual halt after age 15 years in the DS
DS group was 0.36 mm per year, and, in the control group and remaining constant in the control group.
group, it was 0.40 mm per year (Table I). When the The behavior of the basal angle as seen through
734 Alio, Lorenzo, and Iglesias American Journal of Orthodontics and Dentofacial Orthopedics
May 2008
CONCLUSIONS
16. Kisling E. Das schdelwachstum und sein bedentung fr die 36. Baer MJ, Gavan JA. Symposium on bone growth as revealed by
okkluionsverhltnisse bei morbus Down. Stomatol DDR 1976; in vivo markers. Am J Phys Anthropol 1968;29:157-66.
26:785-92. 37. Naval L. Anlisis telerradiogrfico del desarrollo craneofacial en
17. Krumme B. Untersuchungen uber die ontogenetische entwick- pacientes monglicos [thesis]. Zaragoza, Spain: University of
lung des menschlichen schadelbasiswinkels. Z Morphol Zaragoza; 1983.
Antropol 1952;43:331-60. 38. Alonso-Tosso A, Naval L, Hernandez-Vallejo G, Lucas M.
18. Roche AF, Seward FS, Sunderland S. Nonmetrical observations Etude cphalometrique de la base crnienne dans 133 cas de
on cranial roentgenograms in mongolism. Am J Roentgenol syndrome de Down. Rev Stomatol Chir Maxillofac 1985;86:234-
Radium Ther Nucl Med 1961;85:659-62. 40.
19. Dabelow A. Uber die Korrelationen in der pylogenetischen. 39. Menendez M, Alarcon JA, Gonzalez E. Estudio de la morfologa
Entwicklung der Schadelbasisform II. Beziehungenwischen ge- craneofacial en el sndrome de Down. Ortod Esp 1992;33:223-
hirn Schadelbasisform bei den Mammalrru. Gegenbaurs Mor- 32.
phol Jahrb 1931;67:81-113. 40. Suarez-Quintanilla J, Biedma BM, Rodriguez MQ, Mora MT,
20. Roche AF. The cranium in mongolism. Acta Neurol Scand Cunqueiro MM, Pazos MA. Cephalometrics in children with
1966;42:62-78. Downs syndrome. Pediatr Radiol 2002;32:635-43.
21. Lutz A. Uber das wachsatum der schodels (uach messungen an 41. Spitzer R. Development anomalies in teeth and skull in mental
roatgenaufhahmen im seitlichen strahlengang) [dissertation]. Tu- defectives. Int Dent J 1963;3:678-83.
bingen, Germany: University of Tubingen; 1965. 42. Spitzer R. Observations on congenital dentofacial disorders in
22. Fischer- Brandies H, Schmid RG, Fischer-Brandies E. Craniofa- mongolism and microcephaly. Oral Surg Oral Med Pathol
cial development in patients with Downs syndrome from birth to 1967;24:325-32.
14 years of age. Eur J Orthod 1986;8:35-42. 43. Frostad WA, Cleall JF, Melosky LC. Craniofacial complex in the
23. Adams JW. Correction of error in cephalometric roentgeno- trisomy 21 syndrome (Downs syndrome). Arch Oral Biol
grams. Angle Orthod 1940;10:3-13. 1971;16:707-22.
24. Hixon EH. Cephalometric and longitudinal research. Am J 44. Baughan B, Demirjian A. Sexual dimorphism in the growth of
Orthod 1960;46:36-42. the cranium. Am J Phys Anthropol 1978;49:383-90.
25. Klaim U. Pubert e mongolismo (studio auxologico di 10 casi). 45. Latham RA. The sella point and postnatal growth of the human
Minerva Pediatr 1965;17:1248-9. cranial base. Am J Orthod 1972;61:156-62.
26. Rarick RS, Wainer H, Thissen D, Seefeldt V. A double logistic 46. Gosman SD, Vimeland NJ. Facial development in mongolism.
comparison of growth pattern of normal children and children Am J Orthod 1951;37:332-49.
with Downs syndrome. Ann Hum Biol 1975;2:339-46. 47. Benda CE. Growth disorder of the skull in mongolism. Am J
27. Arnell H, Gustafsson J, Ivarsson SA, Anneren G. Growth and Pathol 1940;16:71-86.
pubertal development in Down syndrome. Acta Paediatr Scand 48. Brodie AG. On the growth pattern of the human head from the
1996;85:1102-6. third month to the eighth year of life. Am J Anat 1941;68:209-62.
28. Toledo C, Alembik Y, Aguirre JA, Stoll C. Growth curves of 49. Jensen GM, Clearll JF. Dentoalveolar morphology and develop-
children with Down syndrome. Ann Genet 1999;42:81-90. ment changes in Downs syndrome. Am J Orthod 1973;64:607-
29. Bjork A. Cranial base development. Am J Orthod 1955;41:198- 18.
225. 50. Roche AF, Lewis AB. Sex differences in the elongation of the
30. Dahlberg G. Statistical methods for medical and biological cranial base during pubescence. Angle Orthod 1974;44:279-94.
students. Interscience: New York; 1940. 51. Michejda M, Menolascino FJ. Skull base abnormalities in
31. Calatayud J, Martin G. Bioestadstica en la investigacin odon- Downs syndrome. Ment Retard 1975;13:24-6.
tolgica. 2002.Pues SL; Madrid: 52. James AE Jr, Merz T, Janower ML. Radiological features of the
32. Houston WJB. The analysis of error in orthodontics measure- most common autosomal disorders: trisomy 21-22 (mongolism
ment. Am J Orthod 1983;83:382-90. or Downs syndrome), trisomy 13-15, and the cri du chat
33. Baumrind S, Frantz R. The reliability of head film measurements. syndrome. Clin Radiol 1971;22:417-33.
Am J Orthod 1971;60:111-27. 53. Michejda M. The role of basicranial synchondroses in flexure
34. Richardson A. A comparison of traditional and computerized processes and ontogenetic development of the skull base. Am J
methods of cephalometric analysis. Eur J Orthod 1981;3:15-20. Phys Anthropol 1972;37:143-50.
35. Seward FS, Roche AF, Sunderland S. The lateral cranial silhou- 54. Lewis AB, Roche AF. The saddle angle: constancy or change?
ette in mongolism. Am J Roentgenol 1961;85:653-8. Angle Orthod 1977;47:46-54.