Introduction
Recently, the importance of aesthetic restorations has emerged not only in adults but also in children and adolescents[
1]. It shows that the color reproduction that harmonizes with the oral environment should be considered in addition to pain relief and functional rehabilitation in the anterior restoration. For growing children whose gingiva shape and crown exposure are constantly changing, direct composite resin restoration is preferable in cases of crown fracture, because it allows for a relatively simple procedure and preservation of tooth structure[
2].
The color is recognized by the detection of the wavelengths of reflected visible light by the human eye. The color has properties of hue, brightness, and saturation. The Commission International de L’Eclairage (CIE) defined the color space in 1976, and it has been mainly used for quantifying the color properties recognized by the human eye[
3]. CIE color space system is expressed by L*, a*, and b* values as three-dimensional spatial coordinates. L* value quantifies perceptual lightness, which defines black as 0 and white as 100. a* value is relative to green to red color scale, and b* value is relative to blue to yellow color scale. The color difference, △E
*ab, is defined as a vector in the color space. The formula of the color difference is △E
*ab = ((△L*)
2 + (△a*)
2 + (△b*)
2)
1/2. Perceptibility refers to the perception of the difference between two colors, and acceptability is defined as the clinically acceptable color difference. The perceptibility threshold ranges from △E
*ab = 1.0 to 3.7, and △E
*ab of 2.7 has been set as the clinical perceptibility threshold[
4]. For acceptability, the threshold ranges from △E
*ab = 2.7 to 6.8. The acceptability threshold appears to be greater than the perceptibility threshold[
5].
According to previous studies, the colors of maxillary permanent incisors differ in terms of age and race[
6]. However, these studies were conducted mainly on adult patients, and only a few papers have studied the colors of permanent incisors in children and adolescents[
7]. The changes in color distribution according to age and root developmental stage have rarely been studied in children and adolescents. To this end, the goal of this study is to analyze the color distribution of permanent central and lateral incisors in children and adolescents using a spectrophotometer and to determine the effects of age and root developmental stage on the color distribution.
Discussion
One of the most important and difficult problems in aesthetic restoration is the choice of tooth color. For selecting an accurate color, precise measurement of tooth color is mandatory. As the importance of aesthetic restoration is increasingly emphasized in pediatric dentistry, it is required to precisely match the restoration color to adjacent teeth.
Fracture of permanent incisors is one of the most frequent traumas at all ages, but particularly frequent in ages 7 to 12[
10]. As fracture of permanent incisor due to trauma can entail negative impact on a child’s oral function, aesthetics, and psychological status, a proper recovery of its shape and color is desired[
11]. In order to achieve successful aesthetic restoration in pediatric patients, analyzing the optical characteristics of the central and lateral incisors is critical to accurately matching the color. Direct composite resin restoration is the most viable treatment option for pediatric patients; however, it is challenging to reproduce the tooth colors with composite resin. For this reason, it is important to accumulate data on the colors of maxillary permanent incisors in children and adolescents.
The color measurement using shade guides, which has been traditionally used, has limitations in quantitatively and precisely measuring the color distribution of the natural teeth. Also, shades tend to differ by manufacturer even though they use the same color system. Measurer subjectivity can also be a limitation. Compared to the measurements based on the shade guide, optical measurements by colorimeters and spectrophotometers are considered to be more reliable and objective. Compared to spectrophotometers which use a wide range of wavelength for color measurement including ultraviolet, visible, and infrared, colorimeters use a fixed wavelength in the visible range[
12]. This restricts colorimeters in detecting the reflectance and metamerism[
13]. For this reason, spectrophotometers are considered to be more suitable for precise color measurement. Several studies have proven that spectrophotometers present significantly higher accuracy and reliability in color measurement than colorimeters[
12,
13]. This study used VITA Easyshade
® system, which is a spot-measuring contact-type spectrophotometer, to obtain the color information of teeth. VITA Easyshade
® presented 92.6% in accuracy and 96.4% in reliability[
13]. This is notably higher than those of colorimeters. The availability of various measurement modes, such as “averaged shade determination” mode, “shade determination of the tooth area” mode, “restoration color verification” mode, and “shade tab” mode, is another advantage of VITA Easyshade
® system[
14].
Spot-measuring contact-type spectrophotometers have some limitations. First, edge loss occurs when measuring the reflectance of translucent materials. The light transmitted through a translucent material spreads beyond the measurement area and may not be measured by the device[
15]. This phenomenon can occur if the measurement spot is smaller than the measuring tip, if the measurement surface is not flat, or if the measuring tip cannot contact closely to the measurement surface. With edge loss, the amount of reflected light can be decreased resulting in underestimated actual CIE L*a*b* values[
16]. A VITA Easyshade
® V spectrophotometer includes multiple spectrometers for measuring scattered light at two different distances within the photosphere in the ring in order to minimize edge loss[
17]. To further minimize edge loss, a measuring tip was placed as close as possible and perpendicular to the labial surface of the tooth in each measurement.
Another limitation of the spectrophotometer is the relatively large diameter of the measuring tip compared to the clinical crown length. The diameter of the measuring tip is 5.0 mm. According to Song et al.[
18], the average crown lengths of maxillary permanent central incisors and maxillary permanent lateral incisors are 9.9 mm and 8.5 mm, respectively. To minimize the overlapping measurement area, the measuring tip was placed as closely as possible to the cervical line, incisal edge, or center area of each tooth while measuring the cervical and incisal subregions.
The total surface of central incisors had CIE L*a*b* values of 84.01 ± 3.57, 0.17 ± 0.67, and 24.07 ± 3.43, respectively. The total surface of lateral incisors had CIE L*a*b* values of 82.33 ± 3.38, 0.31 ± 0.56, and 25.99 ± 3.23, respectively. Compared to the color values reported in previous studies conducted on adults ages 18 years and older, CIE L*a*b* values of children and adolescents in this study showed higher L* and b* values[
17,
19]. The inverse correlation of L* and b* values with age was also reported in other studies[
20]. The age-dependent changes in L* values can be interpreted as a result of secondary dentin accumulation which makes the tooth harder, less permeable, and darker in color[
21]. The changes in b* values are considered to be a result of the gradual loss of the enamel layer over time. Consequently, dentin, which is more yellow than the white enamel layer, reveals its color[
22].
In comparison to CIE L*a*b* values of maxillary primary incisors reported in the study conducted by Choi et al.[
23], the color of maxillary permanent incisors in this study is darker and has more yellow shade. This difference between permanent and primary teeth is consistent with the results of the previous studies[
24]. This may be attributed to the fact that primary incisors have more water content than permanent incisors. The structure of primary incisors with thin enamel and dentin layers and a large pulp chamber is also considered to be the cause of the color difference.
Maxillary permanent central incisors presented higher L* values and lower a* and b* values compared to maxillary permanent lateral incisors. Only L* and b* values showed statistically significant differences. Karamen et al.[
6] and Pustina-Krasniqi et al.[
25] reported that L* value of maxillary permanent central incisors is significantly higher than that of maxillary permanent lateral incisors, which is consistent with the results of this study. Unlike the results reported by Karamen et al.[
6], b* value of maxillary permanent central incisors in this study was lower than that of maxillary permanent lateral incisors. This means that maxillary permanent central incisors were brighter and has more blue shade than maxillary permanent lateral incisors in this study population.
Significant differences were observed between each subregion within a tooth, except for L* values between the middle 1/3 and the cervical 1/3 region in maxillary permanent lateral incisors. L* value increased from the incisal 1/3 to the cervical 1/3 region. a* and b* values also increased in the same direction. Previous studies concluded that redness and yellowness increase from the incisal 1/3 region to the cervical 1/3 region[
26,
27]. The main reason for the color difference between subregions is the selective wavelength absorption of dentin. The color is determined by the thickness of dentin and enamel[
28]. Similar to the previous study[
26], the color differences between subregions were larger than the clinical perceptibility threshold of 2.7 in all subjects of this study. This indicates that the color differences are easily distinguishable by the naked eye. The △E
*ab between the subregions were similar to the previous study[
26]. L*, a*, and b* values of the middle 1/3 region showed a strong correlation with those of the cervical 1/3 region and the incisal 1/3 region. According to this correlation, it should be possible to predict the color of other subregions based on the color of one subregion of a tooth. If more data can be accumulated with accurate measurement devices, it will be possible to generate a useful database for predicting the color of one subregion based on the color of another subregion to produce restorations and prostheses with a more suitable color.
L*a*b* values of maxillary permanent central incisors showed a negative correlation with age with a correlation coefficient ρ = 0.914, 0.908, 0.710 respectively, as presented in
Table 7. There was no correlation between age and the color values of maxillary permanent lateral incisors. The majority of maxillary permanent central incisors studied in this study were at the Demirjan’s stage G and H, and the proportion of maxillary permanent central incisors with complete root development tended to increase with patients’ age. On the other hand, maxillary permanent lateral incisors included a considerable number of stage F (
Table 2), and there was no clear pattern of agedependent root development. Based on this observation, it is considered that the correlation of CIE L*a*b* values with age is not as strong in maxillary permanent lateral incisors as in maxillary central incisors between age 7 and 14. Future studies with a larger sample size will be necessary. In both of maxillary permanent central and lateral incisors, the tooth colors were brighter in patients age 10 and younger. According to Kuremoto et al.[
29], age 9.7 is when root development of maxillary permanent incisors is completed, and the mean age of this study population was 10.0 ± 1.5. For this reason, the age of 10 years old was used as the criterion for dividing groups. Similar results were reported in Jahangiri et al.[
20]. The dentin layer becomes harder and less permeable with age as the dental pulp shrinks and secondary dentin forms, resulting in darker tooth color[
22]. At the same time, the pigments and ions can diffuse through enamel, and accumulate at the interface of dentin and enamel and within dentin[
21]. Meera et al.[
30] and Goodkind and Schwabacher[
19] reported that the deposition of secondary dentin mainly contributes to changes in teeth color with age. A limitation of this study was that the number of patients aged 7 and 12 to 14 years old was insufficient to confirm the age-dependent color change. Future studies with a sufficient sample size at each age are necessary.
Although several studies have reported the effect of age on the color of maxillary permanent incisors[
30], there are no reliable databases of the tooth color in relation to root developmental stage. There was no significant color difference between teeth with Demirjian stage F, G and H. The teeth were classified into a group with incomplete root development and a group with complete root development. While L* value decreased with increasing age, the color values did not show statistically significant differences associated with root developmental stage. This differs from the reports of the previous studies[
31], which suggested that teeth become darker and yellower as the root develops, because the accumulation of secondary dentin is a crucial event for the tooth darkening process. Savas et al.[
7] suggested that an incomplete calcification process of teeth with an open apex can cause color differences with root developmental stage, as underdeveloped teeth have low levels of mineralization and porous structures. The reason why it was not possible to confirm the color difference in relation to root developmental stage in this study is possibly because of the sample size differences between the incomplete and complete root development groups. Since only patients with fully erupted incisors were included in this study, those in Demirjian Stage F were only 6.9% among maxillary permanent central incisors and 17.3% among all the teeth studied. Incisors with earlier root developmental stages were not included. Hence this study cannot exactly reflect the impact of root development on tooth color due to insufficient sample size for each stage of root development.
Since there is no standard colorimetric system, each company selects a shade guide of choice to manufacture restorative materials[
32]. VITA classical A1 - D4
® is the most widely used shade guide. It consists of 16 specimens from A1 to D4 with different chroma and brightness. ‘A’ stands for reddish - brown; ‘B’ stands for reddish - yellow; ‘C’ stands for gray; and ‘D’ stands for reddish - gray. The number indicates the brightness, with the smallest number being the brightest[
32]. In maxillary permanent incisors, A2 and B3 shades appear most frequently[
6]. In this study, B3 shade is the most frequent in both maxillary permanent central incisors and lateral incisors which is consistent with the previous studies[
6]. In patients younger than age 7, the best matching VITA shade for both maxillary permanent central and lateral incisors was A1. Considering the small sample size for patients at age 7, future studies with more samples will be necessary to confirm A1 as the best matching VITA shade for age 7. As chronological age increased the best matching VITA shade for each age group showed darker and more yellow shades (
Table 9). Based on this observation, A1 shade seems suitable for the restoration of maxillary permanent incisors in children under the age of 7 years old, and the darker and more yellow resin for older patients.
In this study, the colors of maxillary permanent incisors were measured using the spectrophotometer with known accuracy and reliability. This study was intended to provide a database for the color distribution of maxillary permanent incisors in children and adolescents. It is meaningful that all the color measurements of maxillary permanent incisors were performed with the same spectrophotometer under consistent conditions.
Additional studies with greater sample sizes should be conducted, and the results should be compared to the existing studies, as a limitation of this study is the small sample size of maxillary permanent central incisors with incomplete root development and maxillary permanent lateral incisors with complete root development. The diameter of the measuring tip of the spectrophotometer could have been another limitation. Because of the relatively large diameter of the measuring tip of the spectrophotometer, the color measuring area for the cervical 1/3, middle 1/3 and incisal 1/3 subregions may have overlapped to some extent. Hence, a measuring tip with a smaller diameter is required for accurate color evaluation of tooth subregions.