Cited by 87Gastrointestinal motility and disordersCardiovascular Syncope and Autonomic DisordersGastroesophageal reflux and treatments

Gastrointestinal motility disturbances in patients with orthostatic hypotension

Open access
Camilleri, Michael, Malagelada, Juan-R., Stanghellini, Vincenzo, Fealey, Robert D., Sheps, Sheldon G.·1985·Gastroenterology

Abstract

Orthostatic hypotension syndromes may be associated with visceral denervation, resulting in disturbances of the gastrointestinal and urinary systems. This report analyzes the findings in 9 patients with neurogenic orthostatic hypotension and gastrointestinal symptoms. Antral and proximal small intestinal motor dysfunction was demonstrated in all patients: a significant reduction (p = 0.007) in the number of interdigestive motor complexes during 3 h of fasting (mean 0.4 vs. 1.3 controls); absence of gastric component in interdigestive motor complexes observed; incoordination of fasting and fed antral activity; and development of nonpropagating bursts of phase III-like activity in the intestine that were of at least 2-min duration, high amplitude and frequency, and associated with tonic elevations in baseline pressure. These motor abnormalities may provide a potential means for the diagnosis of impaired autonomic supply to the upper gut.

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Crossref · 10.1016/0016-5085(85)90010-1

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  • Later stages of amyloidosis may show low-amplitude contractions reflecting myopathic infiltration of smooth muscle.

    “Manometric studies suggest that early disease can manifest with motor incoordination consistent with neural involvement, whereas later stages may show low-amplitude contractions reflecting myopathic infiltration of smooth muscle (Battle et al., 1979; Camilleri et al., 1985; Rubinow et al., 1983).”

    From Autonomic nervous system and gastrointestinal manifestations with an emphasis on gastric dysfunction (2026) · cites this paper as Camilleri et al., 1985

    The Discussion (page unavailable) says neural involvement may affect the gut before muscle infiltration in primary amyloidosis and describes very low-amplitude activity as a feature of myogenic pseudoobstruction. But the authors say their patients with amyloidosis showed none of those myogenic features; they did not observe low-amplitude contractions in later-stage amyloidosis. (LLM, conf=0.85)

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  • Manometric studies suggest that early amyloidosis can manifest with motor incoordination consistent with neural involvement.

    “Manometric studies suggest that early disease can manifest with motor incoordination consistent with neural involvement, whereas later stages may show low-amplitude contractions reflecting myopathic infiltration of smooth muscle (Battle et al., 1979; Camilleri et al., 1985; Rubinow et al., 1983).”

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Cites

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Research works printed but not linked: 11

  1. Polinsky RJ, Kopin IG, Ebert MH, Weise V. Pharmacologic distinction of different orthostatic hypotension syndromes. Neurology (NY) 1981;31:1-7.
  2. Shy GM, Drager GA. A neurological syndrome associated with orthostatic hypotension: a clinico-pathological study. Arch Neural 1960;2:511-27.
  3. Khurana RK, Nelson E, Azzarelli B, Garcia JH. Shy-Drager syndrome: diagnosis and treatment of cholinergic dysfunc- tion. Neurology (NY] 1980;30:805-9.
  4. Malagelada J-R, Rees WDW, Mazzotta LJ, Go VLW. Gastric motor abnormalities in diabetic and postvagotomy gastropar- esis: efficacy of metoclopramide and bethanechol. Gastroen- terology 1980;78:286-93.
  5. Aguayo AJ, Nair CPV, Bray GM. Peripheral nerve abnormali- ties in the Riley-Day syndrome. Arch Nemo1 1971;24:106-16.
  6. Young RR, Asbury AK, Adams RD, Corbett JL. Pure pan- dysautonomia with recovery. Trans Am Neurol Assoc 1969; 94:355-7.
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  8. Wichser J, Vijayam N, Dreyfus PM. Dysautonomia-its signif- icance in neurologic disease. Calif Med 1972;117:28-37.
  9. Andersen 0, Lindberg J, Modigh K, Reske-Nielsen E. Sub- acute dysautonomia with incomplete recovery. Acta Neurol Stand 1972;48:510-9.
  10. Low PA, Dyck PJ, Lambert EH, et al. Acute panautonomic neuropathy. Ann Neurol 1983;13:412-7.
  11. Andrade C. A peculiar form of peripheral neuropathy: famil- ial atypical generalized amyloidosis with special involve- ment of peripheral nerves. Brain 1952;75:408-27.

Cited by

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Authors
Camilleri, M., Malagelada, J.-R., Stanghellini, V., Fealey, R. D., & Sheps, S. G.
Affiliations
Mayo Clinic (US)
Venue
Gastroenterology
Publisher
Elsevier BV
Published
1985-06
Volume
88
Issue
6
Pages
1852-1859
ISSN
0016-5085 (ISSN-L)
OpenAlex
W1640809646
Cited by
87
References
2
Citations by year
2026: 2 · 2025: 1 · 2023: 1 · 2022: 2 · 2021: 2 · 2020: 2 · 2016: 1 · 2014: 3 · 2012: 1
FWCI
7.25
Type
journal article
Language
en
Open access
Locations
  • Gastroenterology (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • American Gastroenterological Association
  • National Institutes of Health (5r01am026428-06)
Topics
  • Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
  • Health Sciences › Medicine › Surgery › Cardiovascular Syncope and Autonomic Disorders
  • Health Sciences › Medicine › Gastroenterology › Gastroesophageal reflux and treatments
Keywords
orthostatic hypotension, neurogenic orthostatic hypotension, gastrointestinal motility, small intestine motility, gastric emptying, autonomic dysfunction
MeSH terms
Adult, Aged, Autonomic Nervous System Diseases, Duodenum, Eating, Fasting, Female, Gastrointestinal Motility, Humans, Hypotension, Orthostatic, Jejunum, Male, Manometry, Middle Aged, Norepinephrine, Pyloric Antrum, Sweat

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