Functional Dyspepsia - Evidences in Pathophysiology and Treatment

von: Kazunari Tominaga, Hiroaki Kusunoki

Springer-Verlag, 2018

ISBN: 9789811310744 , 184 Seiten

Format: PDF, Online Lesen

Kopierschutz: Wasserzeichen

Mac OSX,Windows PC für alle DRM-fähigen eReader Apple iPad, Android Tablet PC's Online-Lesen für: Mac OSX,Linux,Windows PC

Preis: 96,29 EUR

eBook anfordern eBook anfordern

Mehr zum Inhalt

Functional Dyspepsia - Evidences in Pathophysiology and Treatment


 

Preface

5

Contents

7

Part I: Etiology

9

Chapter 1: Definition and Prevalence

10

1.1 Definition

10

1.1.1 Background and History

10

1.1.2 Uninvestigated and Investigated Dyspepsia

11

1.1.3 Subgroups

13

1.1.4 Update from Rome III to Rome IV

13

1.2 Epidemiology

14

1.3 Overlap

14

1.3.1 EPS and PDS

14

1.3.2 GERD and FD

15

1.3.3 IBS and FD

16

1.4 Pediatric FD

16

1.5 Limitation of Rome IV

17

References

18

Chapter 2: Genetic Factor

22

2.1 Introduction

22

2.2 Familial Accumulation of FD

23

2.3 The Genotype of GNB3 and FD

24

2.4 FD Clarified by Genetic Association Study in Japan

25

2.5 Conclusions

28

References

28

Chapter 3: Environmental Factors

31

3.1 Introduction

31

3.2 Food and Dyspepsia

32

3.3 Gastrointestinal Infection and Dyspepsia

33

3.4 Acute and Chronic Stress and Dyspepsia

34

3.5 Abuse as an Early-Life Stress

35

3.6 Animal Models for Functional Dyspepsia

36

3.7 Duodenal Inflammation as a Key Mechanism

36

3.8 Summary and Outlook

37

References

38

Part II: Pathophysiology

43

Chapter 4: Neuro-gastroenterology: Central and Autonomic Nervous System

44

4.1 Association of Various Stimuli from Gastrointestinal Tracts with Central Sensation and Abdominal Symptoms in FD

45

4.1.1 Gastric Acid (Chemical Stimulation)

45

4.1.2 Gastric Distension (Mechanical Stimulation)

46

4.2 Association of the CNS with Pathophysiology of FD

47

4.2.1 Regional Activity

48

4.2.2 Serotonin (5-HT) Pathway

48

4.3 Association of Autonomic Nervous System (ANS) with Pathophysiology of Functional Dyspepsia

50

4.4 Therapeutic Possibility for FD via the Neurological Pathway

52

4.4.1 Conclusions

52

References

52

Chapter 5: Neuro-gastroenterology: Enteric Nervous System

55

5.1 Enteric Nervous System

55

5.2 Enteric Glial Cells (EGCs)

56

5.3 Enteric Glial Cells and Functional Gastrointestinal Disorders

58

5.4 Conclusions

60

References

61

Chapter 6: Neuro-gastroenterology: Esophagogastric Function (Motility)

63

6.1 Basic Esophageal Motor Function

63

6.1.1 Upper Esophageal Sphincter (UES)

64

6.1.2 Primary Peristaltic Contraction

64

6.1.3 Secondary Peristaltic Contraction

65

6.1.4 Lower Esophageal Sphincter (LES)

65

6.2 Functional Esophageal Diseases

66

6.2.1 Gastroesophageal Reflux Disease (GERD)

66

6.2.2 Esophageal Motility Disorders

67

6.3 The Relationship Between Functional Dyspepsia (FD) and Functional Esophageal Diseases

68

6.3.1 Commonality Between FD and GERD

68

6.3.2 Involvement of the Nitroxidergic Nerve with the Esophagus and Stomach

69

6.4 Differentiating FD and Functional Esophageal Diseases

69

6.4.1 Difficulty in Differentiating Between FD and GERD

69

6.4.2 Limitations in Clinical Symptoms and Diagnosis

70

6.5 Future Considerations

70

References

71

Chapter 7: Neuro-gastroenterology: Gastroduodenal Function (Motility) and Ultrasonographic Assessment

72

7.1 Gastrointestinal Motility Disorders

73

7.1.1 Test Meal (Consommé Soup)

79

7.2 Parameters

80

7.2.1 Fasting Antral Area (FAA)

80

7.2.2 Gastric Accommodation Reflex (GAR)

81

7.2.3 Gastric Emptying (Gastric Emptying Rate: GER)

81

7.2.4 Antral Contractions (Motility Index: MI)

82

7.2.5 Duodenogastric Reflux (DGR)

82

7.3 US Methods

85

7.3.1 Pharmacometrics

89

7.3.1.1 Acotiamide

90

7.3.1.2 Rikkunshito

91

References

92

Chapter 8: Ghrelin and Functional Dyspepsia

94

8.1 Introduction

95

8.2 Ghrelin

95

8.2.1 Ghrelin Action

95

8.2.2 Ghrelin and FD

98

8.2.3 Ghrelin and Stress-Related Hormones

99

8.2.4 Summary

104

References

104

Chapter 9: Psycho-gastroenterology

107

9.1 Introduction

107

9.2 Epidemiology

108

9.2.1 Psychiatric Comorbidity: Anxiety and Depression

108

9.2.2 Personality: Neuroticism, Perfectionism, and Alexithymia

108

9.2.3 Anxiety and Depression: Predictors of Onset of Functional Dyspepsia

109

9.3 Quality of Life: Physical and Mental

109

9.4 Gut–Brain Pathophysiology

110

9.5 Brain Imaging Studies in Functional Dyspepsia

110

9.5.1 Gastric Hypersensitivity and Anxiety in Brain Function

110

9.5.2 Abnormal Brain Connectivity

111

9.5.3 Abuse History and Brain Function

111

9.5.4 Resting-State Positron-Emission Tomography

112

9.5.5 Brain Function and Functional Dyspepsia with and Without Comorbid Anxiety and Depression

112

9.6 Treatment

112

9.6.1 Placebo

112

9.6.2 Antidepressants

113

9.6.3 Psychological Therapy

114

9.7 Conclusions

114

References

114

Chapter 10: Visceral Hypersensitivity Through Transient Receptor Potential Vanilloid 1 Channels (TRPV1) in Functional Dyspepsia

118

10.1 Introduction

119

10.2 Visceral Pain Induced by Mucosal Inflammation

120

10.3 Transient Receptor Potential (TRP) Channels

120

10.4 TRPV1

121

10.4.1 Physiological Role of TRPV1

121

10.4.2 Inflammatory Bowel Disease Is Associated with Upregulation of TRPV1 in Nerve Fibers of the Colon

124

10.5 Nerve Growth Factor (NGF) and Visceral Hypersensitivity

124

10.6 Conclusion

125

References

126

Part III: Treatment

128

Chapter 11: Efficacy of Acid Suppression Therapy

129

11.1 Background

129

11.2 Cochrane Meta-Analysis (H2RAs and PPIs)

131

11.2.1 H2RA

131

11.2.1.1 H2RA Versus Placebo

131

11.2.1.2 Adverse Events

132

11.2.2 PPI

132

11.2.2.1 PPI Versus Placebo

132

11.2.2.2 Adverse Events

133

11.2.2.3 The Effect of PPIs on Individual Dyspepsia Symptoms

133

11.2.2.4 FD and PPI Metabolism

133

11.2.2.5 Geographical Location

133

11.2.3 H2RA Versus PPI

134

11.3 Antacids and Mucosal Protection

134

11.4 FD and H. pylori Infection

134

11.4.1 FD and H. pylori Eradication Therapy

134

11.4.2 Acid Secretion Inhibitory Drugs and H. pylori Status

135

11.5 Conclusion

135

References

135

Chapter 12: Prokinetics

139

12.1 Introduction

140

12.2 Gastrointestinal Motility and FD

141

12.3 Use of Prokinetics as FD Therapeutic Agents

141

12.4 Usefulness of Acotiamide for Treating FD

142

12.5 Conclusions

144

References

145

Chapter 13: Herbal Medicine

146

13.1 Introduction

147

13.2 Rikkunshito

147

13.3 Hange-koboku-to

149

13.4 Other Agents

149

13.5 Precautions When Using Chinese Herbal Medicines

150

13.6 Conclusion

150

References

150

Part IV: Recent Special Topics: Future Treatment Possibility

152

Chapter 14: Gut Dysbiosis and Its Treatment in Patients with Functional Dyspepsia

153

14.1 Introduction

153

14.2 Postinfectious FD

154

14.3 Gastric Dysbiosis in FD

155

14.4 Duodenal Inflammation and Dysbiosis in FD

156

14.5 Mucosa-Associated Microbiota (MAM) in FD

157

14.6 Treatment for Gut Dysbiosis in FD

159

14.7 Conclusion

161

References

161

Chapter 15: Visceral Hypersensitivity in Functional Dyspepsia (FD): Therapeutic Approaches to FD Based on Suppression of Visceral Hypersensitivity

165

15.1 Pathophysiology of FD in FGID

166

15.2 Visceral Hypersensitivity as One of the Pathophysiologies of FD

166

15.3 Assessment of Visceral Hypersensitivity in FD

167

15.4 Mechanisms of Visceral Hypersensitivity

167

15.5 Foods and Lipids Affecting Visceral Hypersensitivity

168

15.6 Psychosocial Factors Affecting Visceral Hypersensitivity

169

15.7 Therapeutics in FD Based on Suppression of Visceral Hypersensitization

169

15.7.1 Drugs for the Improvement of PDS and EPS in FD

170

15.7.2 Drugs Affecting CNS for Reducing Visceral Hypersensitivity

170

15.7.3 Herbal Medicines

170

15.7.3.1 STW5 (Iberogast®) for the Treatment of FD

170

15.7.3.2 Korean Herbal Medicines for the Treatment of FD

171

15.7.3.3 Japanese Kampo Medicine for the Treatment of FD

171

15.8 Conclusion

172

References

173

Chapter 16: Pancreatic Exocrine Function

176

16.1 Type of Upper Abdominal Symptoms and the Abdominal Region of Symptom Feeling

176

16.1.1 Prevalence Rate of the Common Symptoms and Perception Site of the Abdominal Regions

177

16.1.2 Abdominal Symptoms at the Upper and Lower Epigastrium

180

16.2 Pathogenesis of FD in the Digestive Process

180

16.3 Pancreatic Exocrine Function

181

16.4 Conclusions

183

References

184