Z Gastroenterol 2023; 61(07): 810-817
DOI: 10.1055/a-1833-9494
Originalarbeit

The role of hormones in symptoms and pathophysiology of reflux and esophageal motility disorders

Die Rolle von Hormonen bei Symptomen und Pathophysiologie von Reflux und Ösophagusmotilitätsstörungen
1   Department for Surgery, University Hospital Salzburg, Salzburg, Austria
,
Lisa Wahl
2   Internal Medicine, Salzkammergut-Klinikum Gmunden, Gmunden, Austria
,
Michael Weitzendorfer
1   Department for Surgery, University Hospital Salzburg, Salzburg, Austria
,
1   Department for Surgery, University Hospital Salzburg, Salzburg, Austria
,
Oliver Owen Koch
1   Department for Surgery, University Hospital Salzburg, Salzburg, Austria
,
Klaus Emmanuel
1   Department for Surgery, University Hospital Salzburg, Salzburg, Austria
› Author Affiliations

Abstract

Purpose A few studies suggest that hormones play a role in the motility of the lower esophagus, but data is rare. In this prospective study we evaluated the correlation between hormones (TSH, fT3, fT4, calcitonin, gastrin, and VIP) and gastroesophageal reflux disease (GERD), esophageal motility disorders, and gastrointestinal symptoms.

Methods 100 consecutive patients with reflux symptoms and dysphagia were hospitalized for diagnostic evaluation. Self-reporting questionnaires were handed out and patients routinely underwent serum analysis (TSH, fT3, fT4, calcitonin, gastrin, and VIP), 24-hour-pH-impendance monitoring, and high-resolution manometry.

Results Motility disorders were found in 38 out of 86 patients. There were no correlations between hormones, the DeMeester Score, and the lower esophageal sphincter pressure. A strong inverse relation between calcitonin and the Integrated Relaxation Pressure of the esophagogastric junction was found (r=–0.492; p<0.001). No correlations were found between hormone levels and the responses given in the questionnaires. Positive correlations, however, were found between VIP and gastrointestinal symptoms, as well as correlations between fT3 and dysphagia. Within the group with minor motility disorders, TSH and fT4 correlated with outcomes of the SCL-questionnaire. fT4 correlated with the typical symptoms, as well as the gastrointestinal symptoms (diarrhea, constipation, flatulence). TSH correlated with the typical symptoms. Moreover, a correlation between VIP and gas-bloat-symptoms was found within group II

Conclusions No correlation between TSH, fT3, fT4, gastrin, VIP, calcitonin, and GERD in the sense of acid reflux was found, although calcitonin seems to have an effect on the lower esophageal sphincter.

Zusammenfassung

Hintergrund Ein Zusammenhang zwischen Hormonen und Motilität des Ösophagus wird in einzelnen Studien beschrieben, jedoch gibt es hierfür kaum Daten. In unserer prospektiven Untersuchung wollten wir den Zusammenhang zwischen Hormonen (TSH, fT3, fT4, Calcitonin, Gastrin und VIP) und der gastroösophagealen Refluxkrankheit (GERD), Motilitätsstörungen und gastrointestinalen Symptomen untersuchen.

Methoden 100 Patienten mit Refluxsymptomen und/oder Dysphagie wurden zur stationären Abklärung aufgenommen. Validierte Fragebögen wurden ausgehändigt, 24-Stunden-pH-Impendanz-Monitoring und hochauflösende Manometrie wurden durchgeführt. Des Weiteren erfolgte eine Serumanalyse von TSH, fT3, fT4, Calcitonin, Gastrin und VIP.

Ergebnisse Motilitätsstörungen fanden sich in 38 von 86 Patienten. Es zeigte sich kein Zusammenhang zwischen Hormonen, dem DeMeester-Score und dem Druck des unteren Ösophagussphinkters, jedoch eine starke inverse Korrelation zwischen Calcitonin und der Integrated Relaxation Pressure (IRP) des gastroösophagealen Übergangs (r=–0,492; p<0,001). Des Weiteren zeigten sich keine Zusammenhänge zwischen Hormonwerten und den Ergebnissen von Symptom-Fragebögen. Positive Korrelation zeigte sich bei VIP und gastrointestinalen Symptomen sowie bei fT3 und Dysphagie. In der Gruppe mit „minor motility disorders“ korrelierten TSH und fT4 mit typischen Symptomen und fT4 mit gastrointestinalen Symptomen (Durchfall, Obstipation, Flatulenz) sowie VIP mit „gas-bloat“-Symptomen.

Zusammenfassung Wir konnten keinen Zusammenhang zwischen TSH, fT3, fT4, Gastrin, VIP und Calcitonin mit der gastroösophagealen Refluxkrankheit im Sinne einer Säureexposition zeigen, jedoch scheint Calcitonin einen Effekt auf den unteren Ösophagussphinkter zu haben.



Publication History

Received: 02 January 2022

Accepted after revision: 15 April 2022

Article published online:
13 June 2022

© 2022. Thieme. All rights reserved.

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany

 
  • References

  • 1 Fuchs KH, Babic B, Breithaupt W. et al. EAES recommendations for the management of gastroesophageal reflux disease. Surg Endosc 2014; 28: 1753-1773
  • 2 El-Serag HB, Sweet S, Winchester CC. et al. Update on the epidemiology of gastro-oesophageal reflux disease: A systematic review. Gut 2014; 63: 871-880
  • 3 Vakil N, van Zanten SV, Kahrilas P. et al. The Montreal definition and classification of gastroesophageal reflux disease: A global evidence-based consensus. Am J Gastroenterol 2006; 101: 1900-1920
  • 4 Millan-Billi P, Serra C, Alonso Leon A. et al. Comorbidities, Complications and Non-Pharmacologic Treatment in Idiopathic Pulmonary Fibrosis. Med Sci (Basel) 2018;
  • 5 Chevallay M, Bollschweiler E, Chandramohan SM. et al. Cancer of the gastroesophageal junction: A diagnosis, classification, and management review. Ann N Y Acad Sci 2018;
  • 6 Lee J, Anggiansah A, Anggiansah R. et al. Effects of age on the gastroesophageal junction, esophageal motility, and reflux disease. Clin Gastroenterol Hepatol 2007; 5: 1392-1398
  • 7 İlhan M, Arabaci E, Turgut S. et al. Esophagus motility in overt hypothyroidism. J Endocrinol Invest 2014; 37: 639-644
  • 8 Yaylali O, Kirac S, Yilmaz M. et al. Does hypothyroidism affect gastrointestinal motility?. Gastroenterol Res Pract 2009; 2009: 529802
  • 9 Eastwood GL, Braverman LE, White EM. et al. Reversal of lower esophageal sphincter hypotension and esophageal aperistalsis after treatment for hypothyroidism. J Clin Gastroenterol 1982; 4: 307-310
  • 10 Goyal RK, McGuigan JE. Is gastrin a major determinant of basal lower esophageal sphincter pressure? A double-blind controlled study using high titer gastrin antiserum. J Clin Invest 1976; 57: 291-300
  • 11 Farré R, Aulí M, Lecea B. et al. Pharmacologic characterization of intrinsic mechanisms controlling tone and relaxation of porcine lower esophageal sphincter. J Pharmacol Exp Ther 2006; 316: 1238-1248
  • 12 Hotz J, Goebell H. Pharmacological actions of calcitonin on the gastrointestinal tract and their therapeutical implications. Z Gastroenterol 1981; 19: 637-645
  • 13 Brechmann T, Sperlbaum A, Schmiegel W. Levothyroxine therapy and impaired clearance are the strongest contributors to small intestinal bacterial overgrowth: Results of a retrospective cohort study. World J Gastroenterol 2017; 23: 842-852
  • 14 Chueca E, Lanas A, Piazuelo E. Role of gastrin-peptides in Barrett’s and colorectal carcinogenesis. World J Gastroenterol 2012; 18: 6560-6570
  • 15 Carlsson R, Dent J, Watts R. et al. Gastro-oesophageal reflux disease in primary care: An international study of different treatment strategies with omeprazole. International GORD Study Group. Eur J Gastroenterol Hepatol 1998; 10: 119-124
  • 16 Celasin H, Genc V, Celik SU. et al. Laparoscopic revision surgery for gastroesophageal reflux disease. Medicine (Baltimore) 2017; 96: e5779
  • 17 World medical association (October 2013). WMA Declaration Of Helsinki – Ethical principles for medical research involving human subjects. (Retrieved 03 May 2021). URL. https://www.wma.net/policies-post/wma-declaration-of-helsinki-ethical-principles-for-medical-research-involving-human-subjects/
  • 18 Koch OO, Kaindlstorfer A, Antoniou SA. et al. Subjective and objective data on esophageal manometry and impedance pH monitoring 1 year after endoscopic full-thickness plication for the treatment of GERD by using multiple plication implants. Gastrointest Endosc 2013; 77: 7-14
  • 19 Bredenoord AJ, Fox M, Kahrilas PJ. et al. Chicago classification criteria of esophageal motility disorders defined in high resolution esophageal pressure topography. Neurogastroenterol Motil 2012; 24: 57-65
  • 20 Johnson LF, Demeester TR. Twenty-four-hour pH monitoring of the distal esophagus. A quantitative measure of gastroesophageal reflux. Am J Gastroenterol 1974; 62: 325-332
  • 21 Streets CG, Demeester TR. Ambulatory 24-hour esophageal pH monitoring: why, when, and what to do. J Clin Gastroenterol 2003; 37: 14-22
  • 22 Jamieson JR, Stein HJ, Demeester TR. et al. Ambulatory 24-h esophageal pH monitoring: normal values, optimal thresholds, specificity, sensitivity, and reproducibility. Am J Gastroenterol 1992; 87: 1102-11
  • 23 Johnson LF, Demeester TR. Development of the 24-hour intraesophageal pH monitoring composite scoring system. J Clin Gastroenterol 1986; 8: 52-58
  • 24 Boix-Ochoa J, Lafuente JM, Gel-Vernet JM. Twenty-four hour esophageal pH monitoring in gastroesophageal reflux. Journal of Pediatric Surgery 1980; 15: 74-78
  • 25 Cho YK. How to Interpret Esophageal Impedance pH Monitoring. J Neurogastroenterol Motil 2010; 16: 327-330
  • 26 Pehl C, Keller J, Merio R. et al. 24-Stunden-Osophagus-pH-Metrie. Empfehlungen der Deutschen Gesellschaft für Neurogastroenterologie und Motilität und der Arbeitsgruppe für gastrointestinale Funktionsstörungen und Funktionsdiagnostik der Osterreichischen Gesellschaft für Gastroenterologie und Hepatologie. Z Gastroenterol 2003; 41: 545-556
  • 27 Eypasch E, Williams JI, Wood-Dauphinee S. et al. Gastrointestinal Quality of Life Index: Development, validation and application of a new instrument. Br J Surg 1995; 82: 216-222
  • 28 Belafsky PC, Postma GN, Koufman JA. Validity and reliability of the reflux symptom index (RSI). J Voice 2002; 16: 274-277
  • 29 Allen CJ, Parameswaran K, Belda J. et al. Reproducibility, validity, and responsiveness of a disease-specific symptom questionnaire for gastroesophageal reflux disease. Dis Esophagus 2000; 13: 265-270
  • 30 Lin Z, Kahrilas PJ, Roman S. et al. Refining the criterion for an abnormal Integrated Relaxation Pressure in esophageal pressure topography based on the pattern of esophageal contractility using a classification and regression tree model. Neurogastroenterol Motil 2012; 24: e356-e363
  • 31 Andersen BN, Johansen PB, Abrahamsen B. Proton pump inhibitors and osteoporosis. Curr Opin Rheumatol 2016; 28: 420-425
  • 32 Amato A, Baldassano S, Serio R. et al. Glucagon-like peptide-2 relaxes mouse stomach through vasoactive intestinal peptide release. Am J Physiol Gastrointest Liver Physiol 2009; 296: G678-G684
  • 33 Kuramoto H, Kadowaki M, Yoshida N. Morphological demonstration of a vagal inhibitory pathway to the lower esophageal sphincter via nitrergic neurons in the rat esophagus. Neurogastroenterol Motil 2013; 25: e485-e494