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Updated: Apr 14, 2026

Tilt Testing with Combined Lower Body Negative Pressure: a "Gold Standard" for Measuring Orthostatic Tolerance
Published on: March 21, 2013
Cortical Morphology in Patients with Orthostatic Intolerance
Kyong Jin Shin1, Tae Hyung Kim, Yong Hee Han
1Department of Neurology, Haeundae Paik Hospital, Inje University College of Medicine, Busan, Korea.
Patients with orthostatic hypotension show altered cortical thickness, unlike those with postural tachycardia syndrome. This suggests orthostatic intolerance is a complex condition with distinct neurological underpinnings.
Area of Science:
- Neuroimaging
- Neurology
- Human Anatomy
Background:
- Orthostatic intolerance (OI) is a complex condition affecting autonomic nervous system regulation.
- Understanding the neurological basis of OI subtypes is crucial for targeted treatments.
Purpose of the Study:
- To investigate cortical morphology differences in patients with orthostatic hypotension (OH) and postural tachycardia syndrome (POTS) compared to healthy controls.
- To determine if specific subtypes of OI exhibit distinct neuroanatomical alterations.
Main Methods:
- T1-weighted MRI scans of 30 OI patients (22 OH, 8 POTS) and age/sex-matched controls were analyzed using FreeSurfer.
- Cortical thickness, surface area, volume, and curvature were compared between patient groups and controls.
Main Results:
- Patients with OH showed significantly reduced cortical thickness in several right hemisphere regions (medial orbitofrontal, peri-calcarine, post-central, inferior temporal, lateral occipital) and left peri-calcarine cortex compared to controls.
- No significant differences in cortical thickness, surface area, volume, or curvature were found between POTS patients and controls.
- Other cortical morphology measures (surface area, volume, curvatures) did not differ between OH patients and controls.
Conclusions:
- Cortical morphology is significantly altered in orthostatic hypotension but not in postural tachycardia syndrome.
- These findings support the heterogeneity of orthostatic intolerance, indicating distinct pathophysiological mechanisms for OH and POTS.
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