# Grief‐Related Chest Pain: A Review, Conceptual Analysis, and Integrative Model

**Authors:** Sophia R. Evstigneev, Frank H. Wilhelm, George M. Slavich, David Blum, Annina Seiler

PMC · DOI: 10.1111/psyp.70248 · 2026-01-29

## TL;DR

This paper explores how grief can cause chest pain by analyzing its physiological and psychological mechanisms and proposes a model to better understand and address this under-researched symptom.

## Contribution

The paper introduces a novel theoretical model linking grief to chest pain through psychoneuroimmunological mechanisms.

## Key findings

- Only four empirical studies specifically examined grief-related chest pain without addressing physiological mechanisms.
- The proposed model integrates autonomic, immune, and neuroendocrine pathways in explaining grief-related chest pain.
- Chest pain during grief may serve an evolutionary function by signaling threat and promoting care-seeking behaviors.

## Abstract

Although the death of a loved one is a ubiquitous experience with chest pain a commonly reported symptom, grief‐related chest pain and particularly its physiological mechanisms remain under‐investigated. To address this gap, we adopted Rodger's approach to concept analysis to explore the psychoneuroimmunological mechanisms potentially linking bereavement to chest pain and subsequent health outcomes. A PubMed search, followed by a systematic review of existing literature and clinical observations, yielded 220 articles, of which 49 were included in the conceptual analysis. Notably, only four empirical studies specifically examined grief‐related chest pain, but without underlying physiological mechanisms, while 45 studies explored psychoneuroimmune processes more broadly in the context of loss, grief, and bereavement. Based on these findings, we propose a theoretical model of grief‐related chest pain. The model integrates insights from studies on autonomic, hemodynamic, musculoskeletal, respiratory, neuroendocrine, and immune changes during grief. It summarizes antecedents, attributes, and consequences of grief‐related chest pain, highlighting the putative interrelated roles of physiological, neuroendocrine, and immune pathways. Our model suggests that grief‐related chest pain may constitute a key physical symptom of grief, arising from physiological responses to acute emotional distress and loss. A deeper understanding of the psychobiological mechanisms underlying this phenomenon may provide prognostic insights, inform disease prevention, improve patient care, and guide the development of targeted interventions. Building on this perspective, we also propose a toolkit to facilitate the assessment of grief‐related chest pain in future empirical studies.

We propose that stress‐induced dysregulation of the autonomic, immune, and neuroendocrine systems may contribute to hemodynamic and respiratory changes, potentially leading to grief‐related chest pain, a common yet underexplored physical symptom of grief following the death of a loved one. Given the vital role of the cardiovascular and respiratory systems in the chest, we suggest that chest pain serves an evolutionary function, signaling a perceived threat and promoting care‐seeking behaviors to enhance survival during vulnerable and distressing periods.

## Full-text entities

- **Genes:** VWF (von Willebrand factor) [NCBI Gene 7450] {aka F8VWF, VWD}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, AVP (arginine vasopressin) [NCBI Gene 551] {aka ADH, ARVP, AVP-NPII, AVRP, VP}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, NR3C1 (nuclear receptor subfamily 3 group C member 1) [NCBI Gene 2908] {aka GCCR, GCR, GCRST, GR, GRL}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}, CRH (corticotropin releasing hormone) [NCBI Gene 1392] {aka CRF, CRH1}, IL1A (interleukin 1 alpha) [NCBI Gene 3552] {aka IL-1 alpha, IL-1A, IL1, IL1-ALPHA, IL1F1}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, NPPB (natriuretic peptide B) [NCBI Gene 4879] {aka BNP, Iso-ANP}, POMC (proopiomelanocortin) [NCBI Gene 5443] {aka ACTH, CLIP, LPH, MSH, NPP, OBAIRH}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}
- **Diseases:** fatigue (MESH:D005221), cardiovascular strain (MESH:D013180), chronic pain (MESH:D059350), disordered breathing (MESH:D012891), cardiac repolarization abnormalities (MESH:D018376), Nervous (MESH:D009422), sustained muscular contraction (MESH:D009120), respiratory (MESH:D012131), Cancer (MESH:D009369), muscle tension (MESH:D018781), Takotsubo Syndrome (MESH:D054549), loss (MESH:D016388), neglect (MESH:D058069), Symptom (MESH:D012816), skeletal myopathy (MESH:D009135), pulmonary embolism (MESH:D011655), arterial (MESH:D012078), acute coronary syndrome (MESH:D054058), fibrillation (MESH:D014693), ischemic (MESH:D002545), infection (MESH:D007239), rigidity (MESH:D009127), stroke (MESH:D020521), somatic pain (MESH:D059226), musculoskeletal dysfunction (MESH:D009140), Autonomic Nervous System (MESH:D001342), tachyarrhythmia (MESH:D013610), neuroinflammation (MESH:D000090862), carotid atherosclerosis (MESH:D002340), thrombotic (MESH:D013927), breathlessness (MESH:D004417), hypertension (MESH:D006973), chest discomfort (MESH:D013898), immune dysregulation (OMIM:614878), loss of appetite (MESH:D001068), IHD (MESH:D017202), acute stress cardiomyopathy (MESH:D040701), cardiac distress (MESH:D012128), Coronary artery disease (MESH:D003324), prolonged grief disorder (MESH:D008133), Pain (MESH:D010146), hyperventilation (MESH:D006985), neonatal death (MESH:D066087), Cardiac Syndromes (MESH:D017566), endothelial dysfunction (MESH:D014652), Myocardial Infarction (MESH:D009203), axis (MESH:C566610), anxiety (MESH:D001007), cardiac pathology (MESH:D006331), cardiomyopathy (MESH:D009202), arrhythmias (MESH:D001145), functional decline (MESH:D060825), Inflammation (MESH:D007249), Atrial Fibrillation (MESH:D001281), muscle (MESH:D019042), depressive symptomatology (MESH:D003866), myocardial remodeling (MESH:D064752), death (MESH:D003643), cognitive impairments (MESH:D003072), cardiac ischemia (MESH:D007511)
- **Chemicals:** catecholamine (MESH:D002395), metoprolol (MESH:D008790), adrenaline (MESH:D004837), Cortisol (MESH:D006854), noradrenalin (MESH:D009638), progesterone (MESH:D011374), aspirin (MESH:D001241), oxygen (MESH:D010100)
- **Species:** herpesvirus [taxon 39059], Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12854102/full.md

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Source: https://tomesphere.com/paper/PMC12854102