# Prevalence of Central Sensitization in Postural Tachycardia Syndrome

**Authors:** Gabrielle T. Mathew, Peter Novak

PMC · DOI: 10.1001/jamanetworkopen.2025.53694 · JAMA Network Open · 2026-01-13

## TL;DR

This study found that 86.5% of patients with postural tachycardia syndrome also have central sensitization syndrome, which may worsen their symptoms and disease burden.

## Contribution

The study is the first to quantify the high prevalence of central sensitization syndrome in postural tachycardia syndrome patients.

## Key findings

- 86.6% of POTS patients met criteria for central sensitization syndrome.
- CSS was associated with higher rates of anxiety, depression, fibromyalgia, and other comorbidities.
- Patients with CSS had worse autonomic and sensory symptom scores compared to those without CSS.

## Abstract

What is the prevalence of central sensitization syndrome in postural tachycardia syndrome (POTS)?

This case-control study of 305 patients found a high prevalence (86.5%) of central sensitization syndrome in individuals with POTS.

These findings suggest that co-occurring central sensitization syndrome may exacerbate the disease burden in POTS; enhancing knowledge of this comorbidity could lead to more precise and comprehensive diagnostics and treatment strategies.

This case-control study analyzes the prevalence of central sensitization syndrome in patients with postural tachycardia syndrome among those presenting at a single academic medical center.

A previous study showed a high prevalence of central sensitization syndrome (CSS) in patients with autonomic symptoms. The prevalence of CSS in postural tachycardia syndrome (POTS), a form of dysautonomia, is unknown.

To analyze the prevalence of CSS in POTS.

This case-control study included patients with a POTS diagnosis confirmed by autonomic testing at Brigham and Women’s Faulkner Hospital between 2022 and 2025. Data were analyzed from April to August 2025.

POTS with and without CSS.

Central Sensitization Inventory (to assess central sensitization syndrome [CSS]), COMPASS-31 (autonomic symptoms), Neuropathy Total Symptom Score-6 (NTSS-6, sensory symptoms), PROMIS (global health), and autonomic testing (Valsalva maneuver, deep breathing, sudomotor function, and head-up tilt) with skin biopsies. Primary outcome was the central sensitization inventory score with secondary outcomes individual test performances.

This study included 305 patients with POTS, of whom 264 (86.6%) met criteria for CSS (mean [SD] age, 33.21 [10.75] years; 30 males [11.4%]; 234 females [88.6%]). Patients with CSS compared with those without CSS had longer duration of symptoms, were more frequently female, exhibited higher rates of anxiety (195 [73.9%] vs 20 [48.8%]; P = .002), depression (168 [63.6% vs 14 [34.1%]; P = .001), fibromyalgia (46 [17.4%] vs 0 [0%]; P = .008), irritable bowel syndrome (IBS, 90 [34.1%] vs 7 [17.1%]; P = .046), headaches (176 [66.7%] vs 12 [29.3 %]; P < .001), treatment with antihistamine medication (136 [51.5%] vs 13 [31.7%]; P = .03), psychiatric medication (163 [61.7%] vs 17 [41.5 %]; P = .02), pain medication (127 [48.1%] vs 8 [19.5%]; P = .001), and gastrointestinal medication (82 [31.1%] vs 5 [12.2 %]; P = .02), and had higher COMPASS-31 scores (51.93 [13.23] vs 31.18 [10.49]; P < .001), NTSS-6 scores (11.32 [4.86] vs 4.44 [3.32]; P < .001), NRS scores (3.26 [2.73] vs 0.54 [1.21]; P < .001), and worse PROMIS scores (20.36 [5.45] vs 27.96 [4.73]; P < .001). Autonomic tests showed lower orthostatic end-tidal carbon dioxide (27.59 [6.39] mm HG vs 29.46 [4.68] mm HG; P = .002) and a greater orthostatic decline in cerebral blood flow velocity (17.08 [8.72] cm/sec vs 13.68 [5.04] cm/sec; P < .001) in the CSS group. Both groups had similar prevalence of autonomic failure (223 [84.5%] vs. 33 [80.5%]; P = .67, mostly mild intensity), and abnormal skin biopsy (43% in both groups).

These findings suggest that CSS was common in patients with POTS and may represent a higher-order sequela of cerebrovascular, respiratory, and autonomic dysregulation. This heightened central processing may amplify symptom perception through altered interoceptive signaling. Central sensitization and autonomic impairment may coexist, and management should focus on both conditions.

## Linked entities

- **Diseases:** fibromyalgia (MONDO:0005546), irritable bowel syndrome (MONDO:0005052), anxiety (MONDO:0005618), depression (MONDO:0002050)

## Full-text entities

- **Diseases:** Neuropathy (MESH:D009422), dysautonomia (MESH:D054969), fibromyalgia (MESH:D005356), autonomic failure (MESH:D012791), psychiatric (MESH:D001523), cerebrovascular, respiratory, and autonomic dysregulation (MESH:D002561), IBS (MESH:D053560), CSS (MESH:D003807), pain (MESH:D010146), anxiety (MESH:D001007), irritable bowel syndrome (MESH:D043183), headaches (MESH:D006261), depression (MESH:D003866), gastrointestinal medication (MESH:D005767), POTS (MESH:D054972)
- **Chemicals:** carbon dioxide (MESH:D002245)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC12801080/full.md

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Source: https://tomesphere.com/paper/PMC12801080