Type 1 gastric neuroendocrine tumors show a higher burden of vitamin D deficiency, increased vitamin D supplementation requirements, and a higher prevalence of bone impairment compared with entero-pancreatic NETs, irrespective of dietary habits.
Key Findings
Results
Vitamin D deficiency was significantly more prevalent in the type 1 gNET group compared with the EP-NET group.
VDD prevalence was 92.3% in the gNET group versus 46.2% in the EP-NET group (p = 0.03, OR: 14).
The study included 26 patients total: thirteen with type 1 gNET and thirteen with age- and sex-matched EP-NET.
The cohort was followed at a tertiary referral center between 2010 and 2025.
Dietary adherence did not differ between groups, suggesting disease-specific rather than dietary mechanisms.
Results
Type 1 gNET patients required significantly higher daily cholecalciferol doses for vitamin D normalization than EP-NET patients.
Mean daily cholecalciferol dose was 3198.9 ± 1629 IU/day in gNET versus 1580 ± 1121 IU/day in EP-NET (p = 0.008).
gNET patients more frequently required multiple supplementation formulations (38.5% vs. 0%, p = 0.04).
Multivariable linear regression analysis restricted to VDD patients confirmed that gNET was independently associated with higher daily cholecalciferol dose requirements (p = 0.037).
Time and dose required for normalization, supplementation formulations, bone status, and dietary habits were all analyzed in the study.
Results
Bone impairment was significantly more common in the type 1 gNET group than in the EP-NET group.
Bone impairment, defined as osteoporosis or osteopenia, was present in 61.5% of gNET patients versus 15.4% of EP-NET patients (p = 0.04, OR: 8.8).
This difference was observed irrespective of dietary habits, which did not differ between groups.
Type 1 gNET arises in the setting of autoimmune chronic atrophic gastritis and secondary hypergastrinemia, which may contribute to disease-specific mechanisms of bone involvement.
Background
Type 1 gastric NETs arise in the context of autoimmune chronic atrophic gastritis and secondary hypergastrinemia, which may underlie disease-specific vitamin D malabsorption mechanisms.
Vitamin D deficiency has been associated with bone impairment and adverse outcomes in patients with neuroendocrine tumors generally.
Data specifically addressing gNET and vitamin D status were described as limited prior to this study.
The authors suggest that disease-specific mechanisms rather than dietary differences account for the higher VDD burden and supplementation requirements in gNET.
Methods
The study design was a retrospective, comparative analysis at a single tertiary referral center with an age- and sex-matched control cohort.
A total of 26 patients were included: 13 with type 1 gNET and 13 with EP-NET matched by age and sex.
The study period spanned from 2010 to 2025.
Variables analyzed included VDD prevalence, time and dose required for normalization, supplementation formulations used, bone status, and dietary habits.
Benevento E, Coletta M, Liccardi A, Minotta R, Di Iasi G, Di Nola M, et al.. (2026). Vitamin D Deficiency and Replacement Challenges in Type 1 Gastric Neuroendocrine Tumors: A Comparative Study.. Nutrients. https://doi.org/10.3390/nu18020281