Brief Report: Visual Processing of Faces in Individuals with Fragile X Syndrome: An Eye Tracking Study
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Gaze avoidance is a hallmark behavioral feature of fragile X syndrome (FXS), but little is known about whether abnormalities in the visual processing of faces, including disrupted autonomic reactivity, may underlie this behavior. Eye tracking was used to record fixations and pupil diameter while adolescents and young adults with FXS and sex- and age-matched typically developing controls passively viewed photographs of faces containing either a calm, happy, or fearful expression, preceded by a scrambled face matched on luminance. Results provide quantitative evidence for significant differences in gaze patterns and increased pupillary reactivity when individuals with FXS passively view static faces. Such abnormalities have significant implications in terms of understanding causes of gaze avoidance observed in individuals with FXS.
KeywordsFace processing Fragile X syndrome FMR1 gene Eye tracking Pupil reactivity
Fragile X syndrome (FXS) is the most common cause of inherited mental impairment (Crawford et al. 2001) and, to date, the most common known genetic cause of autism (Cohen et al. 2005). Although it is widely reported that gaze avoidance is a hallmark behavioral feature of FXS (Bregman et al. 1988; Cohen et al. 1991; Garrett et al. 2004), it remains unknown whether abnormalities in the visual processing of faces, including disrupted autonomic reactivity, may contribute to this observed social deficit.
Difficulty for individuals with FXS to establish and maintain eye-gaze during social interactions has been physiologically associated with markedly increased levels of cortisol or autonomic reactivity, suggesting that gaze aversion may be a coping mechanism that serves to reduce negative arousal (Belser and Sudhalter 1995; Hall et al. 2006; Hessl et al. 2002, 2006; Wisbeck et al. 2000). Secretion of cortisol, by means of a cascade of hormones along the hypothalamic-pituitary-adrenal (HPA) axis, involves feedback between several limbic structures, among which the amygdala plays a significant role, and which have been implicated in FXS (Binstock 1995; Hessl et al. 2004; Paradee et al. 1999).
Studies have shown that pupillary responses are regulated by the autonomic nervous system in part in response to level of emotional arousal (Bradley et al. 2008; Ekman et al. 1983; Hess and Polt 1960; Steinhauer et al. 2004). Pupil dilation has been linked with direct electrical stimulation of the amygdala (Gloor 1997) and neuroimaging findings have shown that amygdala activity is associated with an observer’s pupil size as well as is sensitive to the pupil size of others (Demos et al. 2008; Harrison et al. 2006).
The goals of the current study were to examine number of fixations and gaze duration when individuals with FXS viewed photographs of faces with different emotional content, and to measure face-specific changes in pupil diameter as an index of autonomic arousal.
Participants included sixteen individuals with FXS (13 males) and sixteen typically developing (TD) controls (13 males). Individuals with FXS were confirmed to carry the FMR1 full mutation as previously described (Saluto et al. 2005; Tassone et al. 2004). TD participants with no current or past psychiatric diagnoses were recruited from the community. Groups were individually matched on sex and chronological age (t 1, 30 = −0.085, p > .05). At the time of testing, 10 individuals with FXS (8 males) were being treated with at least one class of medication; stimulant (n = 3), antipsychotic (n = 4), and anti-depressant (n = 5). One female control participant was being treated with an anti-hypertensive medication.
Descriptive characteristics of the fragile X syndrome (FXS) and control groups (mean ± SEM)
FXS (n = 16)
TD (n = 16)
Chronological age (years)
16.99 ± 6.8
17.14 ± 6.3
Full scale IQa
58.36 ± 9.8
15.45 ± 7.51
10.46 ± 4.07
Apparatus and Stimuli
All stimuli were presented on a Tobii 1750 binocular eye tracker monitor. This eye tracking system consists of a high-resolution camera embedded in a 17-inch monitor (1,280 × 1,024 pixels resolution, 50 Hz sampling rate, average precision of 0.5° of visual angle). There are several benefits of the Tobii 1750 system that make it conducive to testing individuals with developmental disorders, including approximately 20 cm of tolerance to head-motion in any direction without requiring any head restraints. Stimuli consisted of 60 colored photographs of adult human faces (equal numbers of males and females, different races and ethnicities) from the NimStim Face Stimulus Set (Tottenham 2002), each showing a calm, happy, or fearful expression, and 60 scrambled versions of the face images. Since it was critical that pupil responses following the onset of the face stimulus be independent of a pupillary light reflex, each face and its scramble were matched on mean luminance, and equivalence was confirmed using a photometer (Minolta, LS-100, Osaka, Japan). Face images subtended a 12.12° by 17.19° region (the size of an actual human face) when viewed from a distance of 60 cm, and were presented on a standard 50% grey background.
The experimental protocol was approved by the Institutional Review Board at the University of California, Davis, and informed consent was obtained from all participants or their parents. Following a nine-point calibration, participants were told to view the pictures shown. Each trial consisted of a scrambled face presented for 1 second followed immediately by its matched face for 3 seconds. An inter-trial interval containing a uniform grey screen was shown for 0.5, 1, or 2 s, randomly determined. The order of face presentation was randomized.
Four area-of-interest (AOI) regions were defined for each face: eyes (including the eyebrows), nose, mouth, and other. Scrambled faces included a single AOI around the ellipse. Measures included number of fixations (where a fixation was defined as any data point within a 30 pixel radius for a minimum duration of 100 ms) and proportion of looking time to each AOI region.
Each participant’s pupil data, averaged from both eyes, were first filtered to remove any outlier values corresponding to blinks, loss of tracking data, or large changes in head position. Mean pupil diameter was calculated for 250-ms intervals across the trial duration, time-locked to the onset of the face stimulus. In order to determine the presence of a face-specific pupil response, relative change in pupil size was calculated by subtracting the mean pupil size during the scrambled face from the mean pupil size during each interval of the face presentation, and then “standardized” by dividing by the mean pupil size during the scrambled face. A similar pupil change was calculated for the intervals of the scrambled face, relative to the mean pupil size during the inter-trial interval.
An exploratory analysis revealed that, in individuals with FXS, but not controls, pupil dilation in response to the fearful faces was inversely correlated with number of fixations to the eyes of calm (r = −0.550, p = 0.027), happy (r = −0.612, p = 0.012), and fearful (r = −0.641, p = 0.007] faces, as well as proportion of gaze duration to the eyes of calm faces (r = −0.579, p = 0.019]. There were no significant sex differences within either group on any of the above eye tracking measures. However, a lack of difference may also reflect limitations in statistical power as there were only three girls in each group.
Finally, correlational analyses revealed no significant associations between symptoms of autism in individuals with FXS as measured by the SCQ and ADOS and number of fixations, gaze duration, and changes in pupil diameter in response to the faces. This finding is consistent with studies of gaze aversion in individuals with autism (Dalton et al. 2007; Klin et al. 2002; Speer et al. 2007).
These findings reveal both qualitative and quantitative differences in the way that individuals with FXS visually process static human faces, and to our knowledge, are the first to utilize pupillometry as a measure of autonomic reactivity in individuals with FXS. Individuals with FXS demonstrated fewer fixations and less gaze time to the eye region of faces, and increased pupil reactivity to emotional faces, compared to controls. Importantly, pupil dilation in response to the fearful faces was inversely correlated with number of fixations to the eyes of all faces. This pattern was observed in both males and females with FXS, and was not significantly associated with severity of autism symptomology. Documentation of face processing differences is critical for developing treatment approaches aimed at alleviating the symptoms of social anxiety and has significant potential for use in assessing specific phenotypic outcomes following treatment in clinical research studies (Guastella et al. 2008).
Research has firmly established that FXS and autism are closely associated. Two to six percent of children with autism have the FMR1 mutation (Reddy 2005; Wassink et al. 2001) and approximately 30% of children with FXS are diagnosed with autism and an additional 20–30% have PDDNOS (Bailey et al. 2001; Harris et al. 2008; Kaufmann et al. 2004; Rogers et al. 2001). Researchers have hypothesized that the presence of autism symptoms in FXS exists on a spectrum, such that some individuals with FXS who are also diagnosed with ASD may not be qualitatively different from those without ASD (D. B. Bailey et al. 2004; Lewis et al. 2006).
Our results are in line with research demonstrating that individuals with ASD spend a smaller percentage of time fixating the eyes (Klin et al. 2002; Merin et al. 2007; Pelphrey et al. 2002; Spezio et al. 2007), and thus support the argument that gaze aversion observed in idiopathic autism and in FXS may reflect similarities in underlying network dysfunctions (Belmonte and Bourgeron 2006). Several fMRI studies report reduced activity in the fusiform gyrus (FG) when individuals with autism perform face processing tasks (Dalton et al. 2005; Pierce et al. 2004; Schultz et al. 2000), and fMRI in conjunction with eye tracking has shown that eye-gaze in individuals with autism is positively associated with increased activity and amygdala compared to controls (Dalton et al. 2005). It has therefore been suggested that gaze aversion may be a result of hyperactivation of the amygdala. On the cellular level, van Kooten et al. (2008) recently reported that the FG in post-mortem brains of patients with autism show significant reduction in neuron density and volume, which could provide a neurobiological explanation for the atypical activation of the FG observed in autism. Neuroimaging studies with individuals with FXS have shown reduced FG activation to forward faces and equal FG activation to angled faces, relative to controls (Garrett et al. 2004). Although our interpretations of a common pathophysiological pathway remain speculative until differences in the underlying neural circuitry can be better identified, they are consistent with clinical and research reports of individuals with FXS, with and without autism, becoming overly emotionally aroused and anxious during social situations and therefore averting gaze to facilitate reduction of arousal.
These results should be viewed in light of a few limitations. Including data from groups of individuals with idiopathic developmental delay or autism would help to specify the interpretations and implications of the findings. While our results establish that individuals with FXS exhibit abnormal fixation patterns when viewing static photographs of faces, suggesting that pictures of faces, particularly eyes, are inherently aversive, using dynamic social stimuli that resemble real-life social situations would extend these results. Future studies are required to investigate these findings as they relate to the function of specific brain areas involved in social behavior and emotion regulation.
This work was supported by a grant from the National Institute of Mental Health to DH (MH77554). Thanks are given to the individuals who participated in this study and Alexis L. Schwartz for his assistance in developing specialized data analysis scripts. Data from this study were presented at the 11th International Fragile X Conference, St. Louis, MO, in July, 2008.
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