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. Author manuscript; available in PMC: 2021 Oct 1.
Published in final edited form as: Am J Psychiatry. 2021 Apr 1;178(4):285–287. doi: 10.1176/appi.ajp.2020.21010022

The Elusive Phenotype of Preadolescent Suicidal Thoughts and Behaviors: Can Neuroimaging Deliver on Its Promise?

Randy P Auerbach 1, Henry W Chase 2, David A Brent 2,*
PMCID: PMC8023751  NIHMSID: NIHMS1673236  PMID: 33789457

Vidal-Ribas and colleagues’ elegant paper (1) highlights many of the challenges in identifying biological markers that confer risk for suicidal behaviors in preadolescent youth. Lifetime suicidal thoughts and behaviors were assessed in a large sample (N=7,994) of 9- to 10-year-old youths recruited through the Adolescent Brain Cognition and Development (ABCD) project. Suicidal thoughts and behaviors were most closely associated with child psychopathology, family conflict, and parental psychopathology. The strongest neural correlate was an association between suicidal thoughts and behaviors and decreased thickness of the superior temporal gyrus (STG). Psychosocial and neuroimaging findings only modestly discriminated between those with and without lifetime suicidal thoughts and behaviors. This paper is timely, as the rate of suicidal thoughts and behaviors among preadolescents is increasing rapidly (2), most notably among females as well as Black youth for reasons that are poorly understood. Despite recent efforts, no definitive neural correlates of suicidal thoughts and behaviors have been identified (3).

Although the STG is not a usual suspect in neural markers related to suicide risk, the present study, as the authors note, is not the first to identify an association between structural integrity of this region and suicidal thoughts and behaviors (4). Alterations in resting state functional connectivity have also been observed in a nearby region (Figure 1) (5). The authors’ stringent, unbiased approach greatly diminishes the likelihood that this finding is a false positive, while also ensuring that all regions of the brain received adequate attention. A conventional neurofunctional interpretation of the region does not lend itself to extant theories of suicide, as the region is mostly associated with language. There is, however, a growing body of functional and structural literature that also links the region’s function to social cognition (6, 7). To provide a more comprehensive overview of the region’s functional role, we performed a decoding analysis using the BrainMap database implemented in Mango software (http://ric.uthscsa.edu/mango/)(8). This approach can be useful for providing a broad overview of which cognitive domains might show a functional association with a region’s activity by identifying types of paradigms (e.g., language, sensorimotor, cognition, emotion) that activate the region more often than would be expected by chance. This type of analysis is performed in volume rather than surface space, and thus, the authors kindly provided the peak Montreal Neurological Institute (MNI) coordinates (x=−54.34, y=−44.54, z=4.16) defining the regions of significant difference. We then created a spherical region of interest (ROI) with a 10-mm radius centered on this peak and converted it into Talaraich space. As expected, language-related paradigms (speech/semantics: z’s>5.1) frequently activated the region. However, an intriguing finding was seen just below the standard threshold (z=3), namely social cognition (z=2.93). With regards to suicide, an association between alterations in social behavior and suicide is in line with prior findings, as a common precipitant for pre-adolescent suicide is conflict with parents or peers (9). At the very least, the present analyses provide justification for further targeted analyses of the left STG in suicidal thoughts and behaviors, perhaps including seed-based functional connectivity analyses and paradigms designed to evaluate social behavior.

Figure 1.

Figure 1.

MNI coordinates obtained from Vidal-Ribas et al. (1) MNI coordinates reveal the peak location of structural alteration in youth reporting lifetime suicidal thoughts and behaviors (displayed in blue), overlayed with an alteration in resting state functional connectivity between the dorsal posterior cingulate cortex (dPCC) and the STG region (displayed in red: greater dPCC-temporal functional connectivity among individuals with a lifetime history of suicidal thoughts and behaviors versus healthy controls [5]). Taken together, the STG warrants future investigation, as it may highlight challenges associated with social cognition that confer increased risk for suicidal behaviors.

There are numerous strengths to the paper. Vidal-Ribas and colleagues (1) have been scrupulously careful to control for multiple comparisons and to indicate the clinical significance of statistically significant findings. This respectful and cautious approach to data analysis and interpretation should be a model for the field. In particular, their unbiased and comprehensive approach ensures that the significant finding they observed in the STG is sufficiently strong (Cohen’s d=0.17) to warrant further attention. This state of affairs is not always the case in very highly-powered studies, as rather modest findings can be statistically significant if the power is sufficiently high. Taking a step back from the current findings, however, the broader question is how we build on this and related work in youth suicide. Herein, we offer tenative signposts to guide future work.

First, as the authors acknowledge, a key challenge in interpreting the present data is the temporal and phenomenological breadth of the primary phenotype, lifetime suicidal thoughts and behaviors. Prior research has shown that there may be core differences among youth suicide ideators and attempters (e.g., interpersonal stress exposure [10]; anhedonia and reward processing [11]; familial transmission [12]). Further, there is evidence that functional connectivity and task-based neural activation are sensitive to whether suicidal thoughts and behaviors are current or more distal (13). Accordingly, comparing current ideators with and without a history of recent suicide attempts may elucidate mechanisms that facilitate the transition from ideation to action. Relatedly, longitudinal studies that prioritize enrollment for ideators enriched with those at high risk of making a future suicide attempt—based on a prior attempt history, family history of attempts, or a risk calculator—may validate biological markers implicated in suicide attempts and deaths over time.

Second, suicide risk may be best understood through the identification of interactive, and potentially transactional, processes that shape the emergence of suicidal behaviors (3). Biological diatheses may be a necessary but not sufficient predisposition to engage in suicidal behaviors. In the presence of specific environmental exposures, however, the likelihood of suicidal behaviors may increase. Prior work in adolescence has underscored the importance of peer-related interpersonal stressors often related to romantic attachments as it relates to suicidal behaviors (10), whereas preadolescent suicide decedents often have conflict with family or peers (9). Testing models that account for these developmentally salient environmental exposures and their interaction with biological vulnerability may clarify the pathway for suicidal behaviors among preadolescent youth.

Third, the ABCD project affords access to methodologically rigorous neuroimaging and clinical data. Critically, participants will be followed through preadolesence into early adulthood, a period characterized by a surge in depressive disorders and interpersonal stress exposure (9, 14), which are known correlates of suicidal thoughts and behaviors. Repeated scans during a period of intense neuromaturation will provide an unprecented opportunity to determine whether deviations in normative development are related to suicidal thoughts and behaviors, above and beyond contributions from underlying mental disorders. Enriching the overall ABCD design with ambulatory assessments may illuminate temporal patterns of risk factors leading up to suicidal thoughts and behaviors. Wearables (particularly for younger children) and smartphone apps collect real-time data that provide unique access to dynamic changes in sleep, emotional distress, and social interactions—risk factors repeatedly implicated in suicidal behaviors (15). Coupled with ecological momentary assessment of suicidal thoughts and behaviors, in-lab biological markers—including but not limited to structural and functional neural correlates as well as event-related potentials—can be linked to real-time functioning in the service of clarifying longitudinal predictors of suicidal thoughts and behaviors. It is impractical to follow the entirety of the ABCD sample; however, focusing on an enriched subset of youth at high risk to make a transition from ideation to attempt (e.g., current suicidal ideation with plan and/or suicidal intent) could provide an important roadmap for clarifying central biological markers and associated socioemotional states that inform the timing of suicidal behaviors.

An open question in the field is to what extent neuroimaging—and what modality therein—will improve our understanding of youth suicidal thoughts and behaviors. The relatively low discriminatory power of the suicidal thoughts and behaviors correlates may have prompted Vidal-Ribas and colleagues (1) to be unduly pessimistic in the intepretation of their findings. Given their methodologically rigorous approach, the authors are well-positioned for a longitudinal sequel, accounting for variations in neuromaturation and stress exposures during a critical period of neural and socioemotional development. Integrating these interactive and transactional processes may shed light onto the growing problem of suicidal thoughts and behaviors among preadolescent youth, and perhaps, motivate innovative treatments that reduce the needless loss of young lives.

Acknowledgements:

Funding from the National Institute of Mental Health (NIMH) provided partial support for RPA and DAB (U01MH116923) to prepare this manuscript with additional support from MH115838 for DAB. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health or NIMH.

Disclosures: RPA is a member of the Research Grants Committee for the American Foundation for Suicide Prevention. DAB is a member of the Scientific Advisory Board of the Klingenstein Third Generation Foundation and the Scientific Advisory Council of the American Foundation for Suicide Prevention. He receives research support from NIMH, AFSP, the Once Upon a Time Foundation, and the Beckwith Foundation. He has received royalties from Guilford Press, eRT, and UpToDate, and consulting fees from Healthwise. The design, preparation, review, and approval of the manuscript as well as the decision to submit the manuscript for publication was entirely done by the authors RPA, HWC, and DAB.

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