- Short paper
- Open Access
Reduced orbitofrontal cortical thickness in male adolescents with internet addiction
https://doi.org/10.1186/1744-9081-9-11
© Hong et al.; licensee BioMed Central Ltd. 2013
- Received: 17 October 2012
- Accepted: 6 March 2013
- Published: 12 March 2013
Abstract
Background
The orbitofrontal cortex (OFC) has consistently been implicated in the pathology of both drug and behavioral addictions. However, no study to date has examined OFC thickness in internet addiction. In the current study, we investigated the existence of differences in cortical thickness of the OFC in adolescents with internet addiction. On the basis of recently proposed theoretical models of addiction, we predicted a reduction of thickness in the OFC of internet addicted individuals.
Findings
Participants were 15 male adolescents diagnosed as having internet addiction and 15 male healthy comparison subjects. Brain magnetic resonance images were acquired on a 3T MRI and group differences in cortical thickness were analyzed using FreeSurfer. Our results confirmed that male adolescents with internet addiction have significantly decreased cortical thickness in the right lateral OFC (p<0.05).
Conclusion
This finding supports the view that the OFC alterations in adolescents with internet addiction reflect a shared neurobiological marker of addiction-related disorders in general.
Keywords
- Internet addiction
- Magnetic resonance imaging
- Cortical thickness
- Orbitofrontal cortex
Introduction
Internet addiction has been increasingly recognized as a mental disorder. Recent estimates of its high prevalence in young people, combined with evidence that problematic internet use is a maladaptive behavior with potentially serious occupational and mental health consequences, support the validity of the diagnosis [1]. Nevertheless, there has been much disagreement in the planning for DSM-V about how to conceptualize this relatively new condition, or its core psychopathology [2]. Given this background, identifying the existence of any biological markers would help improve the diagnostic validity [3].
The neural basis of substance addiction has been more extensively studied and is better established compared to other forms of ‘addiction’ (e.g., behavioral addictions). So far, numerous studies in the literature have implicated the role of the orbitofrontal cortex (OFC) in addiction [4–6]. Volkow and colleagues (2000, 2002) suggest that the OFC is one of the most implicated frontal cortical areas in drug addiction [4, 7]. Recently, researchers in our group have reported a longitudinal prospective study result suggesting that structural abnormalities in the OFC might predate and contribute to risk for later cannabis use in young people [8]. Similarly, although few studies have been conducted, the reported functional and structural alterations observed in internet addiction have been relatively consistent in demonstrating altered OFC function (especially in the right hemisphere) and structure [9–14].
We hypothesized that adolescents with internet addiction would show structural abnormalities of the OFC, preferentially in the right hemisphere. Specifically, we conducted a case–control comparison of cortical thickness in adolescents with and without internet addiction, particularly focusing on excessive online gaming, which is among the major subtypes of this disorder [15].
Materials and methods
Subjects
Fifteen right-handed male adolescents with internet addiction were recruited through advertisement in Seoul National University Hospital. The recruitment was performed between February and June 2011. In order to establish the diagnosis of internet addiction we used the Young Internet Addiction Scale (YIAS) [16]. In addition, participants were confined to those reporting to have experienced typical components of addiction with their online gaming including: tolerance, withdrawal, preoccupation with playing it, repeated unsuccessful attempts to reduce or stop it, negatively influenced mood when attempting to reduce it, and neglecting important relationships or activities because of it [17, 18]. In order to exclude any comorbid psychiatric disorders, we used the Kiddie-Schedule for Affective Disorders and Schizophrenia-Present and Lifetime Version (K-SADS-PL) [19]. Healthy male adolescents were recruited through advertisement in local schools and were screened using the same assessment tools described above. Exclusion criteria for both groups were any axis I psychiatric disorder including substance abuse, epilepsy or other neurological disorders, and past history of severe head trauma. The prevalence of internet addiction has been estimated to be much higher in males than in females [1]. Given that males are over-represented in internet-addicted populations, and given time and budget limitations, we decided to focus only on male adolescents. This study was approved by the institutional review board for human subjects at the Seoul National University. All the adolescents and their parents provided written informed consent prior to study entry.
Data acquisition
Whole brain T1-weighted MR images were acquired on a 3T Siemens scanner (Siemens Magnetom Trio Tim Syngo MR B17, Germany) with the following parameters: TR 1900 ms; TE 2.36 ms; inversion time 700 ms; flip angle 9°; voxel size 1.0 mm3; slices 224. Head motions were minimized by filling the empty space around the head with sponge material and fixing the lower jaw with tape.
Image processing
Cortical thickness was estimated using FreeSurfer 5.1.0 (Massachusetts General Hospital, Boston, MA, US), a set of software tools that provides a semi-automated method to investigate brain morphometry. The surface-based stream involves (i) normalization of brain signal intensity, (ii) skull-stripping, (iii) segmentation of gray and white matter, (iv) delineation of the gray-white interface (inner surface), and (v) tracing of the pial (outer) surface. The distance between equivalent vertices in these two surfaces represents the cortical thickness. The whole cortex of each subject was visually inspected and systematically corrected for errors in a blind manner to the group status of the participants. We used our sample to generate an average target surface and the data for each participant were pre-smoothed with a full-width half-maximum Gaussian kernel of 10 mm prior to statistical analyses.
Data analysis
Region-of-interest (ROI)-based analyses were conducted comparing the cortical thickness of the OFC generated by FreeSurfer based on the Desikan-Killiany atlas [20]. More specifically, the Desikan-Killiany atlas defines the lateral and medial divisions of the OFC. The rostral/caudal and medial/lateral boundaries of these two structures are the rostral extent of the lateral orbital gyrus/the caudal portion of the lateral orbital gyrus and the midpoint of the olfactory sulcus/the lateral bank of the lateral orbital sulcus (and/or the circular insular sulcus) for the lateral OFC; and the rostral extent of the medial orbital gyrus/the caudal portion of the medial orbital gyrus (or gyrus rectus) and the cingulate cortex/the medial bank of the superior frontal gyrus for the medial OFC, respectively [20]. Analysis of covariance (ANCOVA) using the general linear model (GLM) was performed with SPSS 19.0 (SPSS Inc., Chicago, IL, USA), and the main effect of group (internet addiction vs. healthy control) was analyzed controlling for age, intelligence quotient (IQ), and intracranial volume (ICV). Results of this analysis were reported with a significance threshold of p<0.05 (two-tailed).
Results
Participant characteristics
The groups of adolescents with and without internet addiction significantly differed in age (13.33±2.84 for internet addiction; 15.40±1.24 for control; p=0.018). IQ was comparable across both groups (103.80±15.84 for internet addiction; 109.06±9.84 for control; p=0.283), and a significant difference in ICV was found (1434.42±158.33 cm3 for internet addiction; 1577.21±183.12 cm3 for control; p=0.030). The YIAS score was significantly higher in the internet addiction group (57.26±16.11 for internet addiction; 37.60±9.72 for control; p=0.000).
ROI-based analyses
Parcellated region-of-interest-based comparison of cortical thickness between adolescents with internet addiction and healthy controls
Comparison | Region | Side | Cortical thickness (mm) | F | p-value | R2 | |
---|---|---|---|---|---|---|---|
Internet | Control | ||||||
Internet < Control | Lateral orbitofrontal | Right | 2.78±0.21 | 2.80±0.18 | 6.609 | 0.016 | 0.395 |
Internet < Control | Cingulate (isthmus) | Right | 2.81±0.31 | 2.84±0.26 | 6.813 | 0.015 | 0.437 |
Internet < Control | Lateral occipital | Left | 2.48±0.15 | 2.48±0.08 | 9.323 | 0.005 | 0.581 |
Internet < Control | Pars orbitalis | Right | 2.75±0.20 | 2.84±0.32 | 5.266 | 0.030 | 0.258 |
Secondary analysis
Vertex-wise whole brain comparison of cortical thickness between adolescents with internet addiction and healthy controls. Red color indicates cortical thickness is greater in adolescents with internet addiction, and blue color indicates cortical thickness is greater in controls.
Discussion
This is the first structural brain imaging study of cortical thickness in adolescents with internet addiction. Consistent with our hypothesis, the results indicated a reduced thickness of OFC in the internet addiction group compared to healthy controls. This finding is in accord with the results of former neuroimaging studies of internet addiction [9–14], and supports the theoretical model of addiction disorders, which emphasizes the involvement of the OFC.
The current finding on internet addiction supports the results of former studies on substance addiction, including ours [8], that have argued that the right OFC plays an important role in the biological mechanism of addiction disorders more broadly. The result of this study is not only in line with numerous other findings in the literature implicating the role of the OFC in addiction [4–6], but also with those indicating that this brain region in the right hemisphere might be particularly important [21].
In this study, only the lateral and not the medial OFC was shown to be significantly different in adolescents with internet addiction. The reason for this finding is not clear, but there have been multiple studies reporting different functions between the lateral and medial OFC, especially in reward-associated decision-making [22]. For example, the medial OFC has been found to be preferentially activated in choices involving immediate rewards, whereas the lateral OFC has been implicated in choices concerning delayed rewards or suppression of previously rewarded responses [23, 24]. It is noteworthy that pars orbitalis, which is laterally adjacent to the lateral OFC, also showed significant cortical thinning in adolescents with internet addiction. This finding supports that the cortical thinning is particularly located in the lateral part of the OFC, without or less involving medial OFC. Further work is warranted on potentially different lateral and medial OFC functions.
Lateral OFC has also been implicated in cognitive flexibility deficits and in the genesis of pathological habits [25]. In this regard, Chamberlain and colleagues (2008) demonstrated that the lateral OFC can be central to neurobiological models of obsessive-compulsive disorder (OCD) [26]. Behavioral addictions are often considered to share similar features with other known disorders including OCD [2], involving specific difficulties in refraining from a certain behavior that causes serious personal consequences. Rotge and colleagues (2008, 2010), based on their previous meta-analyses [27, 28], investigated overlapping brain regions between the anatomical and functional brain maps that showed significant gray matter density change and activity during symptom provocation, respectively, in patients with OCD: the authors found that the only overlapping brain region was the lateral OFC. Recently, Zhou and colleagues (2012) have shown impaired mental flexibility along with poor response inhibition in young adults with internet addiction [29]. The implications of reduced cortical thickness in lateral OFC, in relation to its role in internet addiction as well as other conditions with similar neurobehavioral features, are subject to future studies.
The present study has some important limitations. Above all, a different age distribution between the groups was a critical limitation of this study. However, previous reports on normal brain development have shown that cortical thickness peaks at approximately 8–9 years of age and then global cortical thinning begins afterward [30]. Of note is that all the participants in our study were over this age. Therefore, in adolescents, younger individuals tend to have thicker cortex; our finding of thinner right OFC in the younger internet addiction group thus suggests that the age difference in groups was unlikely to have affected the results. Second, we did not measure the duration of internet addiction. Third, the study participants in the internet addiction group were excessive online gamers, and therefore, the current findings may entail limited generalizability to other subtypes of internet addiction [15].
In summary, the results of the present study indicate preliminary findings of reduced thickness of the right OFC in adolescents with internet addiction. The findings are further suggestive of a shared neurobiological mechanism between internet addiction and other addictive disorders.
Declarations
Acknowledgements
This work was supported by the Seoul National University Brain Fusion Program Research Fund. SBH was supported by a National Research Foundation of Korea (NRF) grant (Global Internship Program) funded by the Korean government (MEST). MY was supported by an NHMRC fellowship grant (#1021973). The funders had no role in the study design, collection, analysis or interpretation of the data, writing the manuscript, or the decision to submit the paper for publication.
Authors’ Affiliations
References
- Ko CH, Yen JY, Yen CF, Chen CS, Chen CC: The association between Internet addiction and psychiatric disorder: A review of the literature. Eur Psychiat. 2012, 27: 1-8.View ArticleGoogle Scholar
- Holden C: 'Behavioral' addictions: do they exist?. Sci. 2001, 294: 980-982. 10.1126/science.294.5544.980.View ArticleGoogle Scholar
- Goldney RD: The utility of the DSM nosology of mood disorders. Can J Psychiatry. 2006, 51: 874-878.PubMedGoogle Scholar
- Volkow ND, Fowler JS: Addiction, a disease of compulsion and drive: involvement of the orbitofrontal cortex. Cereb Cortex. 2000, 10: 318-325. 10.1093/cercor/10.3.318.View ArticlePubMedGoogle Scholar
- London ED, Ernst M, Grant S, Bonson K, Weinstein A: Orbitofrontal cortex and human drug abuse: functional imaging. Cereb Cortex. 2000, 10: 334-342. 10.1093/cercor/10.3.334.View ArticlePubMedGoogle Scholar
- Dom G, Sabbe B, Hulstijn W, van den Brink W: Substance use disorders and the orbitofrontal cortex: systematic review of behavioural decision-making and neuroimaging studies. Br J Psychiatry. 2005, 187: 209-220. 10.1192/bjp.187.3.209.View ArticlePubMedGoogle Scholar
- Goldstein RZ, Volkow ND: Drug addiction and its underlying neurobiological basis: neuroimaging evidence for the involvement of the frontal cortex. Am J Psychiatry. 2002, 159: 1642-1652. 10.1176/appi.ajp.159.10.1642.PubMed CentralView ArticlePubMedGoogle Scholar
- Cheetham A, Allen NB, Whittle S, Simmons JG, Yucel M, Lubman DI: Orbitofrontal volumes in early adolescence predict initiation of cannabis use: a 4-year longitudinal and prospective study. Biol Psychiatry. 2012, 71: 684-692. 10.1016/j.biopsych.2011.10.029.View ArticlePubMedGoogle Scholar
- Dong G, Huang J, Du X: Enhanced reward sensitivity and decreased loss sensitivity in Internet addicts: an fMRI study during a guessing task. J Psychiatr Res. 2011, 45: 1525-1529. 10.1016/j.jpsychires.2011.06.017.View ArticlePubMedGoogle Scholar
- Han DH, Bolo N, Daniels MA, Arenella L, Lyoo IK, Renshaw PF: Brain activity and desire for Internet video game play. Compr Psychiatry. 2011, 52: 88-95. 10.1016/j.comppsych.2010.04.004.PubMed CentralView ArticlePubMedGoogle Scholar
- Han DH, Kim YS, Lee YS, Min KJ, Renshaw PF: Changes in cue-induced, prefrontal cortex activity with video-game play. Cyberpsychol Behav Soc Netw. 2010, 13: 655-661. 10.1089/cyber.2009.0327.View ArticlePubMedGoogle Scholar
- Ko CH, Liu GC, Hsiao S, Yen JY, Yang MJ, Lin WC, Yen CF, Chen CS: Brain activities associated with gaming urge of online gaming addiction. J Psychiatr Res. 2009, 43: 739-747. 10.1016/j.jpsychires.2008.09.012.View ArticlePubMedGoogle Scholar
- Yuan K, Qin W, Wang G, Zeng F, Zhao L, Yang X, Liu P, Liu J, Sun J, von Deneen KM: Microstructure abnormalities in adolescents with internet addiction disorder. PLoS One. 2011, 6: e20708-10.1371/journal.pone.0020708.PubMed CentralView ArticlePubMedGoogle Scholar
- Park HS, Kim SH, Bang SA, Yoon EJ, Cho SS, Kim SE: Altered regional cerebral glucose metabolism in internet game overusers: a 18F-fluorodeoxyglucose positron emission tomography study. CNS Spectr. 2010, 15: 159-166.PubMedGoogle Scholar
- Block JJ: Issues for DSM-V: internet addiction. Am J Psychiatry. 2008, 165: 306-307. 10.1176/appi.ajp.2007.07101556.View ArticlePubMedGoogle Scholar
- Widyanto L, McMurran M: The psychometric properties of the internet addiction test. Cyberpsychol Behav. 2004, 7: 443-450. 10.1089/cpb.2004.7.443.View ArticlePubMedGoogle Scholar
- Christakis DA: Internet addiction: a 21st century epidemic?. BMC Med. 2010, 8: 61-10.1186/1741-7015-8-61.PubMed CentralView ArticlePubMedGoogle Scholar
- Flisher C: Getting plugged in: an overview of internet addiction. J Paediatr Child Health. 2010, 46: 557-559. 10.1111/j.1440-1754.2010.01879.x.View ArticlePubMedGoogle Scholar
- Kaufman J, Birmaher B, Brent D, Rao U, Flynn C, Moreci P, Williamson D, Ryan N: Schedule for Affective Disorders and Schizophrenia for School-Age Children-Present and Lifetime Version (K-SADS-PL): initial reliability and validity data. J Am Acad Child Adolesc Psychiatry. 1997, 36: 980-988. 10.1097/00004583-199707000-00021.View ArticlePubMedGoogle Scholar
- Desikan RS, Segonne F, Fischl B, Quinn BT, Dickerson BC, Blacker D, Buckner RL, Dale AM, Maguire RP, Hyman BT: An automated labeling system for subdividing the human cerebral cortex on MRI scans into gyral based regions of interest. Neuroimage. 2006, 31: 968-980. 10.1016/j.neuroimage.2006.01.021.View ArticlePubMedGoogle Scholar
- Tessner KD, Hill SY: Neural circuitry associated with risk for alcohol use disorders. Neuropsychol Rev. 2010, 20: 1-20. 10.1007/s11065-009-9111-4.PubMed CentralView ArticlePubMedGoogle Scholar
- Mar AC, Walker ALJ, Theobald DE, Eagle DM, Robbins TW: Dissociable Effects of Lesions to Orbitofrontal Cortex Subregions on Impulsive Choice in the Rat. J Neurosci. 2011, 31: 6398-6404. 10.1523/JNEUROSCI.6620-10.2011.PubMed CentralView ArticlePubMedGoogle Scholar
- Elliott R, Dolan RJ, Frith CD: Dissociable functions in the medial and lateral orbitofrontal cortex: Evidence from human neuroimaging studies. Cereb Cortex. 2000, 10: 308-317. 10.1093/cercor/10.3.308.View ArticlePubMedGoogle Scholar
- McClure SM, Laibson DI, Loewenstein G, Cohen JD: Separate neural systems value immediate and delayed monetary rewards. Sci. 2004, 306: 503-507. 10.1126/science.1100907.View ArticleGoogle Scholar
- Rotge JY, Langbour N, Jaafari N, Guehl D, Bioulac B, Aouizerate B, Allard M, Burbaud P: Anatomical alterations and symptom-related functional activity in obsessive-compulsive disorder are correlated in the lateral orbitofrontal cortex. Biol Psychiatry. 2010, 67: e37-e38. 10.1016/j.biopsych.2009.10.007.View ArticlePubMedGoogle Scholar
- Chamberlain SR, Menzies L, Hampshire A, Suckling J, Fineberg NA, del Campo N, Aitken M, Craig K, Owen AM, Bullmore ET: Orbitofrontal dysfunction in patients with obsessive-compulsive disorder and their unaffected relatives. Sci. 2008, 321: 421-422. 10.1126/science.1154433.View ArticleGoogle Scholar
- Rotge JY, Langbour N, Guehl D, Bioulac B, Jaafari N, Allard M, Aouizerate B, Burbaud P: Gray matter alterations in obsessive-compulsive disorder: an anatomic likelihood estimation meta-analysis. Neuropsychopharmacol. 2010, 35: 686-691. 10.1038/npp.2009.175.View ArticleGoogle Scholar
- Rotge JY, Guehl D, Dilharreguy B, Cuny E, Tignol J, Bioulac B, Allard M, Burbaud P, Aouizerate B: Provocation of obsessive-compulsive symptoms: a quantitative voxel-based meta-analysis of functional neuroimaging studies. J Psychiatry Neurosci. 2008, 33: 405-412.PubMed CentralPubMedGoogle Scholar
- Zhou Z, Yuan G, Yao J: Cognitive biases toward Internet game-related pictures and executive deficits in individuals with an Internet game addiction. PLoS One. 2012, 7: e48961-10.1371/journal.pone.0048961.PubMed CentralView ArticlePubMedGoogle Scholar
- Shaw P, Greenstein D, Lerch J, Clasen L, Lenroot R, Gogtay N, Evans A, Rapoport J, Giedd J: Intellectual ability and cortical development in children and adolescents. Nature. 2006, 440: 676-679. 10.1038/nature04513.View ArticlePubMedGoogle Scholar
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