# Putative sympathetic-predominant subtype in body-first Parkinson’s disease is associated with accelerated cognitive decline

**Authors:** Xining Liu, Zhiheng Xu, Xiuyuan Li, Chenqin Xu, Shiyu Li, Tianyu Hu, Chen Chen, Xiaoniu Liang, Yilin Tang, Jian Wang

PMC · DOI: 10.3389/fnagi.2026.1747748 · Frontiers in Aging Neuroscience · 2026-02-16

## TL;DR

A specific type of Parkinson’s disease linked to the sympathetic nervous system may lead to faster cognitive decline compared to another type.

## Contribution

Identified a potential link between sympathetic-predominant body-first Parkinson’s and accelerated cognitive decline.

## Key findings

- SPS patients showed significantly faster decline in MMSE scores compared to PPS patients.
- Progression of motor and non-motor features was similar between the two subtypes.

## Abstract

Parkinson’s disease (PD) can be classified into brain-first and body-first subtypes based on the initial site of α-synuclein pathology. Postmortem studies further suggest that body-first PD may be divided into two phenotypes: sympathetic-predominant subtype (SPS) and parasympathetic-predominant subtype (PPS). However, studies on longitudinal clinical characteristics of the two putative body-first subtypes are limited.

We aim to investigate the clinical features of these subtypes.

In a cohort of 73 body-first PD patients, we identified 14 patients with orthostatic hypotension (OH) without constipation (putative SPS) and 40 with constipation without OH (putative PPS). Linear mixed models were used to assess disease progression.

Over follow-up, SPS patients exhibited a significantly faster decline in MMSE scores compared with PPS patients (p = 0.045). Progression of other motor and non-motor features was comparable between the groups.

These findings indicated that sympathetic-predominant body-first PD may be associated with a more rapid trajectory of cognitive decline, although the observed effect was modest and warrants cautious interpretation.

## Linked entities

- **Diseases:** Parkinson’s disease (MONDO:0005180)

## Full-text entities

- **Genes:** SNCA (synuclein alpha) [NCBI Gene 6622] {aka NACP, PARK1, PARK4, PD1}
- **Diseases:** constipation (MESH:D003248), Lewy pathology (MESH:D005598), Depression (MESH:D003866), REM Sleep Behavior Disorder (MESH:D020187), cognitive decline (MESH:D003072), impairment of the nigrostriatal dopaminergic system (MESH:D009422), Movement Disorder (MESH:D009069), thermoregulatory abnormalities (MESH:D000014), OH (MESH:D007024), SPS (MESH:C535673), PPS (MESH:D001342), gastroenterologic disorders (MESH:D009358), MDS (MESH:D009190), hearing (MESH:D034381), PD (MESH:D010300), blurred (MESH:D014786), cerebral hypoperfusion (MESH:D002547), syncope (MESH:D013575), /bowel symptoms (MESH:D012778)
- **Chemicals:** levodopa (MESH:D007980), parkinsonian medications (-), 123I-MIBG (MESH:D019797)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

29 references — full list in the complete paper: https://tomesphere.com/paper/PMC12950674/full.md

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Source: https://tomesphere.com/paper/PMC12950674