Prevalence of neurodegenerative/demyelinating disorders in patients with achalasia

Author:

Jerie Martin12,Vackova Zuzana34,Vojtech Zdenek25,Mares Jan3,Meluzinova Eva6,Krajciova Jana47,Vymazal Josef8,Cerna Hana9,Martinek Jan34

Affiliation:

1. First Faculty of Medicine, Charles University , 12108 Prague , Czech Republic

2. Department of Neurology, Na Homolce Hospital , 15000 Prague , Czech Republic

3. Department of Hepatogastroenterology, Institute for Clinical and Experimental Medicine , 14021 Prague , Czech Republic

4. Institute of Physiology, First Faculty of Medicine, Charles University , 12108 Prague , Czech Republic

5. Charles University, Third Faculty of Medicine , 10000 Prague , Czech Republic

6. Department of Neurology, Second Faculty of Medicine, Charles University, Motol University Hospital , 15000 Prague , Czech Republic

7. ResTrial s.r.o. , 16000 Prague , Czech Republic

8. Department of Radiology, Na Homolce Hospital , 15000 Prague , Czech Republic

9. Sarkamed s.r.o. , 27401 Slany , Czech Republic

Abstract

Abstract Introduction Esophageal achalasia is a primary motility disorder. Although the exact pathogenesis is unknown, autoimmune, and neurodegenerative processes seem to be involved similarly to neurodegenerative and/or demyelinating disorders (NDDs). We hypothesized that the prevalence of NDD may be higher among patients with achalasia and vice versa as the background pathogenetic mechanisms are similar. Methods This was a prospective, comparative questionnaire-based study. Patients with achalasia and patients with NDD were enrolled. Selected patients with achalasia were thoroughly examined by a neurologist and selected patients with NDD were examined by a gastroenterologist to confirm or rule out NDD or achalasia. We assessed the prevalence of both achalasia and NDD and compared them with their prevalence in general population. Results A total of 150 patients with achalasia and 112 patients with NDD were enrolled. We observed an increased prevalence of NDD among patients with achalasia (6.0% (9/150); 95% CI (confidence interval): 3.1–11.2%) as compared to the estimated 2.0% prevalence in general population (p = 0.003). Although 32 out of 112 patients (28.6%) with NDD reported dysphagia, we did not observe significantly increased prevalence of achalasia in these patients (1.8% (2/112) vs 0.8% in general population, p = 0.226). Conclusion The prevalence of NDD was significantly higher among patients with achalasia (6.0%) compared to general population (2.0%), suggesting an association of these disorders. Large-volume studies are necessary to confirm this finding.

Publisher

Walter de Gruyter GmbH

Subject

General Neuroscience

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