# The Burden of Preoperative Stress: Biological Mechanisms and Postoperative Outcomes

**Authors:** Aaqib Syed, Tallita Menezes, Andrew Bisenius, Aleksandar Sic, Nebojsa Nick Knezevic

PMC · DOI: 10.3390/brainsci16020219 · Brain Sciences · 2026-02-11

## TL;DR

Preoperative stress affects surgical outcomes through biological mechanisms and can lead to complications, but it may be modifiable with targeted interventions.

## Contribution

This review highlights biological pathways linking preoperative stress to adverse outcomes and emphasizes the need for stress assessment in perioperative care.

## Key findings

- Preoperative stress is associated with increased analgesic needs, postoperative pain, and complications.
- Cortisol and interleukin-6 mediate stress effects through immune, metabolic, and nervous system pathways.
- Stress-related pain modulation is evident in both experimental and clinical settings.

## Abstract

Preoperative psychological stress is a highly prevalent but mostly underrecognized factor influencing perioperative physiology and postoperative outcomes. This narrative review synthesizes current evidence on the known mechanisms connecting preoperative stress to adverse surgical outcomes, with particular emphasis on HPA axis functioning, cortisol dynamics, inflammatory signaling and pain modulation. Elevated preoperative anxiety affects a substantial proportion of surgical patients and is consistently associated with increased analgesic and anesthetic requirements, higher postoperative pain intensity, greater risk of chronic postsurgical pain, neuropsychiatric complications, metabolic dysregulation and postoperative infections. Stress-related elevations in cortisol and pro-inflammatory cytokines, particularly interleukin-6, appear to mediate these effects through interactions with immune, metabolic, and central nervous system pathways. Stress-related pain modulation is reflected not only in experimental models but also in clinically measurable outcomes, underscoring its relevance for perioperative care. Despite growing recognition of these associations, standardized strategies for integrating stress assessment and biomarkers into perioperative risk stratification remain limited. Given that preoperative stress is potentially modifiable, targeted psychological, analgesic, and metabolic interventions may represent valuable opportunities to improve recovery, reduce complications, and prevent pain chronification.

## Linked entities

- **Proteins:** IL6 (interleukin 6)
- **Chemicals:** cortisol (PubChem CID 5754)

## Full-text entities

- **Genes:** Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, NOS3 (nitric oxide synthase 3) [NCBI Gene 4846] {aka EC-NOS, ECNOS, MYMY8, NOSIII, cNOS, eNOS}, IL6ST (interleukin 6 cytokine family signal transducer) [NCBI Gene 3572] {aka CD130, CDW130, GP130, HIES4, HIES4A, HIES4B}, HSP90AA1 (heat shock protein 90 alpha family class A member 1) [NCBI Gene 3320] {aka EL52, HEL-S-65p, HSP86, HSP89A, HSP90A, HSP90N}, POMC (proopiomelanocortin) [NCBI Gene 5443] {aka ACTH, CLIP, LPH, MSH, NPP, OBAIRH}, CRH (corticotropin releasing hormone) [NCBI Gene 1392] {aka CRF, CRH1}, SERPINA6 (serpin family A member 6) [NCBI Gene 866] {aka CBG}, ICAM1 (intercellular adhesion molecule 1) [NCBI Gene 3383] {aka BB2, CD54, P3.58}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, JUNB (JunB proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 3726] {aka AP-1}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, PNMT (phenylethanolamine N-methyltransferase) [NCBI Gene 5409] {aka PENT, PNMTase}, PRRT2 (proline rich transmembrane protein 2) [NCBI Gene 112476] {aka BFIC2, BFIS2, DSPB3, DYT10, EKD1, FICCA}, AVP (arginine vasopressin) [NCBI Gene 551] {aka ADH, ARVP, AVP-NPII, AVRP, VP}, VCAM1 (vascular cell adhesion molecule 1) [NCBI Gene 7412] {aka CD106, INCAM-100}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}, PIK3R1 (phosphoinositide-3-kinase regulatory subunit 1) [NCBI Gene 5295] {aka AGM7, GRB1, IMD36, p85, p85-ALPHA, p85alpha}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** cognitive dysfunction (MESH:D003072), acute and chronic pain (MESH:D059787), tissue injury (MESH:D017695), hypoxia (MESH:D000860), memory dysfunction (MESH:D008569), metabolic dysregulation (MESH:D021081), metabolic (MESH:D008659), neuroendocrine dysregulation (MESH:D018358), hyperalgesia (MESH:D006930), coronary calcification (MESH:D003323), POIs (MESH:D013530), Delirium (MESH:D003693), postoperative (MESH:D019106), postoperative delirium (MESH:D000071257), inflammatory cytokines (MESH:D000080424), nausea and vomiting (MESH:D020250), Depression (MESH:D003866), chronic pain (MESH:D059350), abdominal, chest and low back pain (MESH:D015746), Anxiety (MESH:D001007), atrophy (MESH:D001284), acute myocardial infarction (MESH:D009203), mental illness (MESH:D001523), neurocognitive dysfunction (MESH:D019965), infection (MESH:D007239), diabetic (MESH:D003920), CPSP (MESH:D010149), sleep disturbances (MESH:D012893), hypertension (MESH:D006973), Pain (MESH:D010146), death (MESH:D003643), malnutrition (MESH:D044342), burnout (MESH:D002055), atherosclerosis (MESH:D050197), injury to (MESH:D014947), anemia (MESH:D000740), neuropsychiatric complications (MESH:D008107), headache (MESH:D006261), Chronic inflammation (MESH:D007249), astrogliosis (MESH:D005911), carotid plaques (MESH:D016893), Hyperglycemia (MESH:D006943)
- **Chemicals:** glucose (MESH:D005947), serotonin (MESH:D012701), cholesterol (MESH:D002784), nitric oxide (MESH:D009569), blood glucose (MESH:D001786), hexosamine (MESH:D006595), calcium (MESH:D002118), ROS (MESH:D017382), norepinephrine (MESH:D009638), propofol (MESH:D015742), NAD+ (MESH:D009243), alcohol (MESH:D000438), glycogen (MESH:D006003), testosterone (MESH:D013739), Wortmannin (MESH:D000077191), Ouabain (MESH:D010042), peroxynitrite (MESH:D030421), steroid (MESH:D013256), phosphatidyl-inositol-(3,4,5)-trisphosphate (MESH:C060974), epinephrine (MESH:D004837), polyol (MESH:C024617), Cortisol (MESH:D006854), NADPH (MESH:D009249), BH4 (MESH:C003402), opiates (MESH:D053610), benzodiazepines (MESH:D001569), sodium (MESH:D012964), Ca2+ (-), NO (MESH:D009614)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

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## References

131 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938735/full.md

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Source: https://tomesphere.com/paper/PMC12938735