We propose an exploratory clinical study (NEURO-CARD-2) that employs simultaneous functional near-infrared spectroscopy (fNIRS) and electrocardiography (ECG) to investigate interhemispheric dysfunction in the dorsolateral prefrontal cortex (DLPFC) and its relationship with autonomic sympathetic activation in women with recurrent pregnancy loss (RPL) and comorbid anxiety. Using a standardized multisensory aversive emotional stimulation paradigm, the study will assess cortical and cardiac responses within the framework of the Brain-Heart-Emotion interaction model. The objective is to identify neurobiological signatures underlying emotion-autonomic dysregulation in this population, thereby informing future development of precision-targeted interventions.
Recurrent pregnancy loss (RPL), defined as two or more consecutive pregnancy losses before 24 weeks' gestation, affects an estimated 2-5% of reproductive-aged couples worldwide. Beyond its profound reproductive consequences, RPL carries a heavy psychological burden: approximately 50% of affected women experience chronic anxiety. This emotional distress is more than a mental health concern-it triggers persistent sympathetic activation, evidenced by elevated resting heart rate and diminished heart rate variability (HRV), thus compounding cardiovascular and reproductive risks in a self-reinforcing pathogenic cycle. Modern psycho-cardiology paradigms, backed by statements from the American Heart Association, underscore the intimate interplay between emotional dysregulation and autonomic dysfunction. Yet the neural mechanisms linking altered central emotion regulation to cardiac autonomic outcomes in women with RPL remain largely elusive-especially in those with comorbid anxiety. Emerging theories in interoceptive neuroscience suggest that higher-order brain regions could serve as shared neural substrates mediating both anxiety and sympathetic overactivation. In particular, the dorsolateral prefrontal cortex (DLPFC), a critical node within the cognitive control and central autonomic networks, stands out. Evidence from neuroimaging and neuromodulation studies demonstrates hemispheric asymmetry in the DLPFC: the right DLPFC is implicated in threat processing, anxiety generation, and sympathetic arousal, whereas the left DLPFC supports cognitive reappraisal, emotional inhibition, and parasympathetic modulation. We propose a Brain-Heart-Emotion interaction model in which effective and adaptive autonomic responses depend on synchronized bilateral activation of the DLPFC during negative emotional challenge. Conversely, functional decoupling-manifested as right-lateralized DLPFC dominance-may undermine emotion regulation capacity and precipitate sympathetic overdrive. In women with RPL and comorbid anxiety, this decoupling is posited to drive the convergence of emotional dysregulation and cardiac dysfunction, thereby elevating the risk of adverse reproductive and cardiovascular outcomes. To test this hypothesis, we have designed a prospective, exploratory clinical study employing simultaneous functional near-infrared spectroscopy (fNIRS) and electrocardiography (ECG) during a standardized multisensory emotional provocation paradigm. We will investigate patterns of interhemispheric DLPFC activation and their relationship to heart rate dynamics in women with recurrent pregnancy loss (RPL), in the presence versus absence of comorbid anxiety, within the proposed Brain-Heart-Emotion framework. If confirmed, these findings will provide both mechanistic insight and empirical justification for neurobiologically informed, precision-targeted interventions. In particular, they may support the application of inhibitory neuromodulation targeting the right DLPFC, with the potential to deliver multidimensional therapeutic benefits-including enhanced emotional regulation, restoration of autonomic balance, reduced long-term cardiovascular risk, and improved reproductive outcomes in this high-risk population.
Study Type
OBSERVATIONAL
Enrollment
50
To elicit hemodynamic responses in the dorsolateral prefrontal cortex (DLPFC) and activate the sympathetic nervous system, we used a standardized multisensory aversive stimulation protocol comprising: (i) Visual stimuli: 72 high-arousal images from the GAPED database (moral violations, legal violations, fear-related) shown in 12 blocks (6 images/block, 5 s each) with 20 s baseline and 30 s stimulation; (ii) Auditory stimuli: each block paired with 30 s of calibrated 90 dB(A) high-frequency narrowband white noise (4 kHz center frequency), shown to increase heart rate; (iii) Cold-pain stimuli: during each block, participants placed both hands on 0 °C ice-filled bottles for pain-induced sympathetic activation. This tri-modal task reliably provokes DLPFC engagement and autonomic responses.
The Second Affiliated Hospital of Shenyang Medical College
Shenyang, Liaoning, China
RECRUITINGCentral Hospital Affiliated to Shenyang Medical Collage
Shenyang, Liaoning, China
RECRUITINGInterhemispheric asymmetry of DLPFC activation during aversive emotional stimulation (group × hemisphere interaction).
The primary outcome is the interaction between diagnostic group (RPL with anxiety vs RPL without anxiety) and hemisphere (right vs left dorsolateral prefrontal cortex, DLPFC) in response to aversive emotional stimulation, assessed using a linear mixed-effects model (LME). The model includes fixed effects for group, hemisphere, and their interaction, with random intercepts specified for participants. Post hoc pairwise comparisons of estimated marginal means are conducted using linear contrasts, and Bonferroni correction is applied to account for multiple comparisons. We hypothesise that participants with RPL and comorbid anxiety will exhibit significantly greater right-lateralised DLPFC activation relative to those without anxiety, reflecting altered interhemispheric asymmetry in emotion regulation pathways.
Time frame: Single-session fNIRS-ECG protocol
Group difference in interhemispheric synchronization of DLPFC activity
Interhemispheric synchronization in the dorsolateral prefrontal cortex (DLPFC) is assessed using wavelet transform coherence (WTC) between homologous fNIRS channels. Coherence values are averaged across the frequency band of interest (0.01-0.08 Hz) and time window, background-corrected using the 3-minute resting period, and Fisher z-transformed. Group-level statistical comparisons will be then performed on the resulting z-values.
Time frame: Single-session fNIRS-ECG protocol
Group difference in averaged heart rate increase during aversive emotional stimulation
For time-domain heart rate variability analysis, preprocessed R-R intervals are resampled at 11 Hz and filtered using a 4th-order low-pass Butterworth filter (cutoff: 0.1 Hz) to suppress respiratory and cardiac noise. Data will be segmented into 40-second epochs (10 s pre-stimulation and 30 s stimulation), and baseline correction will be applied. Mean heart rate elevation during stimulation is computed for each of the 12 blocks and averaged per participant. Between-group comparisons will be performed on the resulting values.
Time frame: Single-session fNIRS-ECG protocol
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