General
Why ZES useful model of Chr HG
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Chronic hypergastrinemia (Chr. HG) |
ZES patients have lifelong Chr. HG
Delayed diagnosis-6yrs
Less 20% cured lifelong
30–40% = FSG levels in range of PPIs in non-ZES pts, rest have > FSG levels
All forms of circulating gastrin including amidated, NH2,COOH extended forms
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General
Why ZES useful model of long-term PPI use
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Lifelong need for potent gastric antisecretory drugs—PPIs drug of choice |
>80% ZES patients take PPI lifelong
Frequently take hi doses PPI
Regularly followed for acid control and other side-effects
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ECL hyperplasia/gastric carcinoids
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Chronic hypergastrinemia (Chr. HG) |
All ZES patients have ECL hyperplasia
Advanced ECL changes including dysplasia is seen both sporadic and MEN1/ZES
ECL changes are more advanced in MEN1/ZES
Carcinoids are very uncommon in sporadic ZES which resemble non-ZES PPI users
23% of MEN1/ZES have gastric carcinoids
Sporadic ZES more resembles chronic PPI users than CAG/PA patients which have high incidence of inflammation ± atrophy and frequently develop carcinoids
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Esophageal, gastric, pancreatic adenocarcinomas
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Chronic hypergastrinemia (Chr. HG) |
Limited data but no evidence for increased incidence in ZES
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Colorectal cancer
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Chronic hypergastrinemia (Chr. HG) |
Limited data but no evidence for increased incidence in ZES2
Two studies show increased rectal/colonic mucosal increased proliferative rates in ZES
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Nutrient malabsorption (Fe, Ca)
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PPI-induced Hypo-/Achlorhydria |
Limited data but no evidence for malabsorption in ZES
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Nutrient malabsorption (VB12)
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PPI-induced Hypo-/Achlorhydria |
Two studies report decreased VB12 levels in in ZES2
One ZES study correlates low serum levels in VB12, but not folate levels with use of PPIs, duration of PPI use and with the degree of PPI-induced acid hyposecretion.
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Hypomagnesemia
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Unclear = mechanism |
Uncommonly reported in ZES patients showing that it is not dose-related or related to length of treatment with PPIs
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Bone fractures
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Unclear = mechanism |
No data in ZES2
ZES poor model to study this in as 20–25% have MEN1 with hyperparathyroidism, which causes bone disease; a proportion have malabsorption prior to diagnosis which could contribute to bone disease, and high proportion had low VB12 levels from long-term PPI that could contribute
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Rebound hypersecretion after stopping PPI
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Unclear = mechanism |
Studies of ZES patient’s post-curative resection of gastrinoma have provided insights into very long-term effects of PPI treatment/Chr HG on post drug acid secretory effects.
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