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February 12, 2026PAIN Reports2 citationsOpen Access

Baseline vagal tone and pain reactivity: linking autonomic function to endogenous pain inhibition in women

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EGEinav GozanskyUniversity of HaifaHOHadas Okon-SingerMax Planck Institute for Human Cognitive and Brain SciencesIWIrit Weissman‐FogelUniversity Health Network

Key Result

Baseline vagal tone (RMSSD) predicted better conditioned pain modulation efficiency during the follicular phase in healthy women (β = −1.05, P = 0.010).

Key Points

  • This research investigates the relationship between baseline vagal tone and pain inhibition, particularly across different phases of the menstrual cycle.
  • Sixty-seven healthy females completed psychological questionnaires and psychophysical pain assessments.
  • Participants underwent tonic heat pain testing alone and during conditioned pain modulation (CPM).
  • Electrocardiograms recorded heart rate variability during baseline and pain conditions categorized by menstrual phase.
  • The interaction of resting RMSSD and menstrual cycle phase predicted CPM efficiency.
  • Vagal tone was linked to pain inhibition primarily during the follicular phase (β = −1.05, P = 0.010).
  • Higher RMSSD levels correlated with increased CPM magnitude, indicating better pain modulation.

Structured PICO

Does baseline vagal tone associate with endogenous pain inhibition in healthy females, and is this influenced by the menstrual cycle?

P
Population
67 healthy females
I
Intervention
Assessment of heart rate variability (vagal tone via RMSSD) and conditioned pain modulation (CPM)
O
Outcome
Conditioned pain modulation (CPM) efficiency and its association with resting root mean square of successive differences (RMSSD)surrogate

Baseline vagal tone is associated with more efficient endogenous pain inhibition in healthy females, specifically during the follicular phase of the menstrual cycle.

Limitations

  • Lack of within-subject design across the menstrual cycle

Abstract

Abstract Introduction: Conditioned pain modulation (CPM) is a laboratory test of the efficacy of endogenous pain inhibition. Although the vagus nerve is thought to contribute to analgesia via descending inhibitory pathways, its role in CPM remains unclear. In addition, as vagal tone fluctuates across the menstrual cycle due to hormonal changes, the menstrual cycle's influence on the vagal–CPM association warrants investigation. Methods: Sixty-seven healthy females completed psychological questionnaires and underwent psychophysical assessments (1-minute tonic heat pain THP given alone and during CPM). An electrocardiogram was recorded at rest, and in 1-minute segments before, during, and after the THP alone, as well as during a conditioning stimulus (CPM paradigm). Heart rate variability was assessed using time- and frequency-domain indices. Menstrual phase was categorized as either follicular or luteal based on standard cycle-length division. Results: The interaction between the resting root mean square of successive differences (RMSSD) and the menstrual cycle predicted better CPM efficiency. Post-hoc analysis revealed that the vagal–CPM association emerged solely in the follicular phase (β = −1.05, P = 0.010). Nevertheless, psychological factors did not influence the vagal–CPM association. The RMSSD broadly changed under pain with conditioning compared to baseline, with higher levels of RMSSD positively associated with CPM magnitude. Conclusions: The findings suggest a tentative menstrual cycle–dependent association between baseline vagal tone and pain inhibition in healthy females. Further, greater vagal activity contributes to more efficient pain inhibition. Future studies should use within-subject designs to examine how interactions between vagal and sympathetic activity across the menstrual cycle influence pain modulation.

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Cite This Study

Gozansky et al. (2026) studied this question. Baseline vagal tone (RMSSD) predicted better conditioned pain modulation efficiency during the follicular phase in healthy women (β = −1.05, P = 0.010).

synapsesocial.com/papers/698d6d9f5be6419ac0d529bdhttps://doi.org/10.1097/pr9.0000000000001390
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