This exploratory clinical study, NEURO-CARD-2, will use simultaneous functional near-infrared spectroscopy (fNIRS) and electrocardiography (ECG) to investigate interhemispheric dysfunction in the dorsolateral prefrontal cortex (DLPFC) and its association 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 a Brain-Heart-Emotion interaction framework. The objective will be to identify neurobiological signatures of emotion-autonomic dysregulation in this population and to inform the future development of precision-targeted interventions.
Recurrent pregnancy loss (RPL), defined as two or more consecutive pregnancy losses before 24 weeks of gestation, affects an estimated 2% to 5% of reproductive-aged couples worldwide. In addition to its reproductive consequences, RPL is associated with a substantial psychological burden, and approximately 50% of affected women experience chronic anxiety. This emotional burden has been linked to persistent sympathetic activation, including elevated resting heart rate and reduced heart rate variability, which may contribute to cardiovascular and reproductive risk. Contemporary psycho-cardiology models, including statements from the American Heart Association, emphasize the close relationship between emotional dysregulation and autonomic dysfunction. The neural mechanisms linking altered central emotion regulation to cardiac autonomic outcomes in women with RPL remain insufficiently characterized, particularly in those with comorbid anxiety. Emerging work in interoceptive neuroscience suggests that higher-order brain regions may provide shared neural substrates for anxiety and sympathetic overactivation. The dorsolateral prefrontal cortex (DLPFC), a key node in the cognitive control network and central autonomic network, is of particular interest. Neuroimaging and neuromodulation studies have shown hemispheric asymmetry within the DLPFC. The right DLPFC has been associated with threat processing, anxiety, and sympathetic arousal, whereas the left DLPFC has been associated with cognitive reappraisal, emotional inhibition, and parasympathetic modulation. A Brain-Heart-Emotion interaction model underlies this study. Within this framework, effective autonomic adaptation during negative emotional challenge is hypothesized to depend on coordinated bilateral DLPFC recruitment. Functional decoupling, expressed as right-lateralized DLPFC dominance, may weaken emotion regulation capacity and promote sympathetic overactivation. In women with RPL and comorbid anxiety, this pattern is hypothesized to contribute to the convergence of emotional dysregulation and cardiac dysfunction, with potential implications for reproductive and cardiovascular risk. To evaluate this hypothesis, this prospective exploratory clinical study will use simultaneous fNIRS and ECG during a standardized multisensory emotional provocation paradigm. Patterns of interhemispheric DLPFC activation and their associations with heart rate dynamics will be examined in women with RPL with and without comorbid anxiety within the proposed Brain-Heart-Emotion framework. If confirmed, the findings may provide mechanistic insight and empirical support for neurobiologically informed precision-targeted interventions. Potential implications may include support for inhibitory neuromodulation targeting the right DLPFC, with possible benefits for emotional regulation, autonomic balance, long-term cardiovascular risk reduction, and reproductive outcomes in this high-risk population.
Study Type
OBSERVATIONAL
Enrollment
70
Participants will undergo a standardized multisensory aversive stimulation paradigm during simultaneous fNIRS and ECG recording. The protocol will use a block design with 12 stimulation blocks, each comprising a 20 s resting phase followed by a 30 s multisensory stimulation phase. During stimulation, participants will view six negative high-arousal images per block selected from the Geneva Affective Picture Database, while concurrently being exposed to time-locked band-limited white noise calibrated to approximately 90 dB(A) and placing both hands on a 0.5 liter bottle filled with ice water maintained at approximately 0 °C. The auditory stimulus will have spectral energy restricted to 2-6 kHz. This standardized multisensory protocol will be used to elicit negative affect and sympathetic arousal.
The Second Affiliated Hospital of Shenyang Medical College
Shenyang, Liaoning, China
Central Hospital Affiliated to Shenyang Medical College
Shenyang, Liaoning, China
157 Hospital of Liaoning Health Industry Group
Shenyang, Liaoning, China
242 Hospital Affiliated to Shenyang Medical College
Shenyang, Liaoning, China
Group-dependent hemispheric asymmetry of DLPFC activation during aversive emotional stimulation (group × hemisphere interaction)
The primary endpoint will be the group-by-hemisphere interaction in task-evoked DLPFC HbO activation during aversive emotional stimulation, comparing women with recurrent pregnancy loss (RPL) with anxiety versus without anxiety. Hemisphere will be defined as right versus left DLPFC, measured within the same participant. The participant-level activation metric will be the DLPFC HbO response estimate (β) derived from the prespecified fNIRS analysis pipeline. The primary hypothesis will be tested using a linear mixed-effects model (LME) fitted by restricted maximum likelihood, with prespecified covariates including age, education, body mass index, miscarriage etiology category, and resting heart rate. The primary confirmatory test will evaluate whether the right-minus-left difference in DLPFC activation differs by group.
Time frame: Single-session fNIRS-ECG protocol (Day 1)
Group difference in interhemispheric synchronization of DLPFC activity
Interhemispheric DLPFC synchronization will be assessed using wavelet transform coherence (WTC) between homologous left and right DLPFC HbO signals. For each participant, coherence values will be averaged across the task-relevant low-frequency band (0.01-0.08 Hz) and across the stimulation period, background-corrected using the 3-minute resting period, and Fisher z-transformed to yield a participant-level synchronization metric. Between-group differences will be summarized descriptively and tested using a two-sample independent t test and a covariate-adjusted linear regression model with prespecified covariates. Prespecified supporting analyses will repeat the same computation and inferential framework across four additional prefrontal subregions to assess spatial specificity.
Time frame: Single-session fNIRS-ECG protocol (Day 1)
Group difference in mean heart-rate increase during aversive emotional stimulation
Autonomic reactivity will be assessed as the mean heart-rate increase during aversive stimulation relative to the resting baseline, derived from ECG over the prespecified task window using a uniform preprocessing pipeline across participants. Preprocessed R-R intervals will be resampled at 11 Hz, filtered with a fourth-order low-pass Butterworth filter with a 0.1 Hz cutoff, detrended, segmented into 40-second epochs consisting of 10 seconds before stimulus onset and 30 seconds during stimulation, and baseline-corrected using the 10-second prestimulus period. The resulting heart-rate increase will be averaged across the 12 blocks for each participant. Between-group differences will be tested using a two-sample independent t test and a covariate-adjusted linear regression model.
Time frame: Single-session fNIRS-ECG protocol (Day 1)
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.