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      Understanding the Effects of Prenatal Alcohol Exposure Using Three Dimensional Facial Imaging

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      , M.S., , Ph.D.
      Alcohol Research & Health
      National Institute on Alcohol Abuse and Alcoholism

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          Abstract

          One of the (at least theoretically) most easily detectable features of fetal alcohol syndrome (FAS) and fetal alcohol spectrum disorders (FASD) is a distinct pattern of facial characteristics. However, in many children prenatally exposed to alcohol, these characteristics are expressed only subtly, making it difficult to correctly identify children with these disorders. To date, several studies have used conventional two-dimensional images to develop computerized programs assisting in the identification of individuals with FAS or FASD. However, many of the subtle features of prenatal alcohol exposure cannot be visualized using two-dimensional images. Therefore, researchers at the Collaborative Initiative on Fetal Alcohol Spectrum Disorders (CIFASD; http://www.cifasd.org) have been using a special camera system that can generate three-dimensional images, which allows them to explore the advantages of using such images to identify subtle facial differences between individuals who were exposed to alcohol prenatally and individuals who were not. This approach may help investigators and clinicians to better understand the complications that may arise from prenatal alcohol exposure. For example, CIFASD researchers can use facial measurements or shapes obtained from the three-dimensional images to predict the presence of FAS, examine associations between facial shapes and cognitive deficiencies, or better understand how the facial growth of a person with FAS compares with facial growth in someone not prenatally exposed to alcohol. Through an international consortium, CIFASD has been addressing these questions in various age groups as well as different ethnic groups. The Three-Dimensional Camera System and Image Analysis The camera system used to obtain the three-dimensional images consists of two pods attached at each end of a long arm that is mounted to a standard camera tripod (see figure 1). Each pod contains three cameras and two flashes so that a total of six photographs are generated. These six photographs, which eventually comprise the three-dimensional image, are obtained in 1.5 milliseconds, similar to normal flash photography. The attached laptop computer system uses special software to automatically stitch together the six photographs (see figure 2), generating the final three-dimensional image in less than 2 minutes (see figure 3). Although the camera system looks big and bulky, it can easily be taken apart and packed into two cases. As a result, CIFASD researchers have the ability to transport the camera anywhere in the world, take three-dimensional images of dozens of children within a day, and electronically transfer these images to a secure computer for analysis. The three-dimensional images can be analyzed in several ways. One of the simpler analytic strategies is to measure the length, width, or height of various portions of the face, such as the length of the eye, width of the forehead, or height of the upper face (figure 4). CIFASD investigators have used these measurements to evaluate whether these parameters differ in people with and without prenatal alcohol exposure. The analyses found that by using a subset of these measurements as predictor variables in a statistical method called logistic regression, one can accurately classify children in a given sample into two groups: those with FAS and those who were not exposed to alcohol prenatally. For example, when studying children from Cape Town, South Africa, CIFASD researchers identified a set of measurements that could correctly classify 94 percent of children with FAS and 91 percent of children without prenatal alcohol exposure (Moore et al. 2007). Using the same statistical approach, but with a group of children from Helsinki, Finland, the researchers also identified a set of facial measurements that correctly classified 96 percent of children with FAS and 91 percent of those without prenatal alcohol exposure. Interestingly, the sets of facial measurements that best identified the respective groups differed between the South African and Finnish samples. However, in both groups small eye width was one of the parameters that helped to predict FAS (Moore et al. 2007). These results support previous observations that small eye widths are a key feature distinguishing individuals with FAS and without prenatal alcohol exposure. CIFASD researchers now are seeking to understand why some unique facial features helped predict group membership in the South African and Finnish samples. One possibility is that these differences are caused by facial variation attributable to ethnicity. Alternatively, the differences may be related to age differences between the two samples because the South African children, on average, were much younger than the Finnish participants, and previous studies already noted that the facial characteristics of people with FAS change with age (Mutsvangwa et al. 2010; Streissguth et al. 1991). Another way to analyze three-dimensional images is to place specific landmarks on the images and then connect the landmarks with lines that generate shapes (see figure 5) (Mutsvangwa and Douglas 2007), a method that originally was proposed by Clarren and colleagues (1987). Using an approach called morphometrics, one then can look at differences between the shapes found in the faces of children prenatally exposed to alcohol and those found in the faces of nonexposed children. To achieve this, the shapes obtained from the faces of all subjects are aligned statistically so that they then can be compared between the two groups (i.e., people with FAS and control individuals) (Douglas and Mutsvangwa 2010). Similarly, one can compare the shapes between younger and older individuals (Mutsvangwa et al. 2010). Using this approach, researchers can examine what information specific shapes can provide about an individual’s face—such as the fullness of the face, slower growth in certain facial areas, or asymmetries between the two sides of the face. Thus, CIFASD researchers have found that differences exist in the shape of particular facial regions between children with FAS and controls (Klingenberg et al. 2010). In addition, certain differences in facial shapes appear to be related to performance on tests that measure cognitive function (i.e., IQ) (Wetherill et al. 2009). Findings such as these are important because they begin to allow researchers to better understand how prenatal alcohol exposure affects development, both in the face and in the brain. Potential Applications of the Three-Dimensional Imaging System The three-dimensional facial imaging system has several potential applications that may aid researchers and clinicians in identifying individuals with FAS and delineating the consequences of prenatal alcohol exposure. For example, the technology may allow researchers to track how the facial features associated with prenatal alcohol exposure change as an individual grows up. Studies currently are underway in a group of children seen in South Africa in 2005, when most of them were 5 years old, and then again in 2009, when they were 9 years of age. Analyzing data from both time points, CIFASD researchers found that during this time period, children with FAS exhibited faster growth than non–alcohol-exposed children in particular parts of the face. As a result, the facial features most characteristic of FAS (i.e., small eyes and small face) became larger, making the facial features less distinct (Mutsvangwa et al. 2010; Wetherill et al. 2010). This observation confirms previous reports by doctors and clinicians who specialize in the effects of prenatal alcohol exposure that the facial features of children with FAS become less obvious as the children age. Another application currently being explored by members of CIFASD is the opportunity to study changes in the faces of younger children. To this end, CIFASD is working with a team of pediatricians at Tygerberg Hospital, a part of Stellenbosch University Medical School, South Africa, to take three-dimensional images of babies at 1 month of age and again at 12 months. The investigators hope to enroll about 1,200 babies in the study, about 600 of whom will have been prenatally exposed to alcohol. Extensive data is available on the children’s prenatal alcohol exposure, which will allow the research team to study how the babies’ faces change during the first year depending on the amount and timing of the prenatal alcohol exposure. Finally, studies involving participants of differing ages, races, and ethnicities will allow the CIFASD team to devise new ways to identify children with prenatal alcohol exposure. Because it is essential for the children’s prognosis to initiate interventions as early as possible, this approach using the three-dimensional camera and image analysis can lead to earlier detection of and intervention for those at greatest risk.

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          Most cited references9

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          Fetal alcohol syndrome in adolescents and adults.

          Fetal alcohol syndrome is a specific recognizable pattern of malformation. Manifestations in 61 adolescents and adults suffering from alcohol teratogenesis are presented. After puberty, the faces of patients with fetal alcohol syndrome or fetal alcohol effects were not as distinctive. Patients tended to remain short and microcephalic, although their weight was somewhat closer to the mean. The average IQ was 68, but the range of IQ scores widely varied. Average academic functioning was at the second- to fourth-grade levels, with arithmetic deficits most characteristic. Maladaptive behaviors such as poor judgment, distractibility, and difficulty perceiving social cues were common. Family environments were remarkably unstable. Fetal alcohol syndrome is not just a childhood disorder; there is a predictable long-term progression of the disorder into adulthood, in which maladaptive behaviors present the greatest challenge to management.
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            Prenatal alcohol exposure alters the patterns of facial asymmetry.

            Directional asymmetry, the systematic differences between the left and right body sides, is widespread in human populations. Changes in directional asymmetry are associated with various disorders that affect craniofacial development. Because facial dysmorphology is a key criterion for diagnosing fetal alcohol syndrome (FAS), the question arises whether in utero alcohol exposure alters directional asymmetry in the face. Data on the relative position of 17 morphologic landmarks were obtained from facial scans of children who were classified as either FAS or control. Shape data obtained from the landmarks were analyzed with the methods of geometric morphometrics. Our analyses showed significant directional asymmetry of facial shape, consisting primarily of a shift of midline landmarks to the right and a displacement of the landmarks around the eyes to the left. The asymmetry of FAS and control groups differed significantly and average directional asymmetry was increased in those individuals exposed to alcohol in utero. These results suggest that the developmental consequences of fetal alcohol exposure affect a wide range of craniofacial features in addition to those generally recognized and used for diagnosis of FAS. Copyright © 2010 Elsevier Inc. All rights reserved.
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              Unique facial features distinguish fetal alcohol syndrome patients and controls in diverse ethnic populations.

              Effective management of fetal alcohol spectrum disorders (FASD) is dependent on the timely and reliable diagnosis of affected individuals. There are significant diagnostic difficulties because of the reduced prominence of facial features as children age to adulthood as well as potential population or ethnic differences in the most characteristic alcohol-related facial features. A total of 276 subjects were recruited from 4 sites (Cape Town, South Africa; Helsinki, Finland; Buffalo, New York; and San Diego, California) and completed a detailed dysmorphology evaluation to classify subjects as either fetal alcohol syndrome (FAS; 43%) or control (57%). Computerized anthropometry was employed to identify facial features that could distinguish FAS patients from controls across a wide age range and across ethnically disparate study populations. Subjects were placed into 1 of 4 populations based on their ancestry (Cape Coloured, Finnish Caucasian, African American, or North American Caucasian). Analyses performed in each of the 4 study populations were able to identify a unique set of variables which provided excellent discrimination between the 2 groups (FAS, control). In each study group, at least one ocular-related measurement, shortened palpebral fissure, reduced outer canthal width, or reduced inner canthal width, was included in the final classification model. We found measurements that reflected reduced size of the eye orbit to be a consistent feature discriminating FAS and controls across each study population. However, each population had a unique, though often overlapping, set of variables which discriminated the 2 groups, suggesting important ethnic differences in the presentation of FAS. It is possible that these differences were accentuated by the wide age distribution of the study subjects.
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                Author and article information

                Journal
                Alcohol Res Health
                Alcohol Res Health
                ARH
                Alcohol Research & Health
                National Institute on Alcohol Abuse and Alcoholism
                1535-7414
                1930-0573
                2011
                : 34
                : 1
                : 38-41
                Author notes

                L eah W etherill, M.S., is a statistician, and T atiana F oroud, P h.D., is a professor in the Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana.

                Article
                arh-34-1-38
                3860560
                23580039
                ca24f7d7-9132-4716-9ccc-f9776073afe8
                Copyright @ 2011

                Unless otherwise noted in the text, all material appearing in this journal is in the public domain and may be reproduced without permission. Citation of the source is appreciated.

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