Paper Summary
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Vitamin D: Some Sunshine for Certain Groups, But Not a Universal Cure-All
This clinical practice guideline, based on a systematic review of randomized trials, suggests empiric vitamin D supplementation for children and adolescents (1-18 years) to prevent nutritional rickets and potentially reduce respiratory tract infections, adults over 75 years to reduce mortality risk, pregnant individuals to lower risks of complications such as pre-eclampsia, and those with high-risk prediabetes to reduce progression to diabetes. The guideline generally suggests *against* routine vitamin D supplementation beyond the recommended dietary allowance for other adult populations and *against* routine 25(OH)D screening for all populations considered, due to insufficient evidence of benefit.
Possible Conflicts of Interest
The guideline discloses potential conflicts of interest for several panel members related to research funding, consulting roles, or ownership of stock in pharmaceutical companies. Management strategies were implemented to mitigate these potential conflicts, such as limiting involvement in discussions of specific products.
Identified Weaknesses
Many of the trials used in the meta-analysis had limitations, including variations in vitamin D dosages, co-administration of calcium, allowing participants to take other supplements, and variable baseline 25(OH)D levels. These limitations make it difficult to draw definitive conclusions about the optimal dosage and effectiveness of vitamin D supplementation for specific health outcomes.
Concomitant supplement use
Several trials allowed participants to remain on their pre-existing vitamin D supplements, and many of these supplements were in line with the recommended dietary allowance. This could lead to bias towards the null in trials evaluating empiric vitamin D supplementation.
Limited data on empiric supplementation
The guideline focuses on empiric supplementation, without prior 25(OH)D testing, and acknowledges the scarcity of clinical trials specifically designed to address this strategy. Furthermore, due to variations in trial designs and supplementation regimens, providing specific recommendations for dosages and thresholds for 25(OH)D testing was challenging.
Limited racial/ethnic diversity
The guideline acknowledges that the majority of trials included participants of European descent, which limits the generalizability of the findings to other ethnic or racial groups with varying vitamin D metabolism and sun exposure.
Lack of evidence for screening
There was no clinical trial evidence found to support routine screening for 25(OH)D in the general population or in those with obesity or dark complexion, making it difficult to define optimal target levels of 25(OH)D for disease prevention in these populations.
Rating Explanation
This clinical practice guideline provides a comprehensive and detailed overview of the evidence related to vitamin D supplementation for the prevention of various diseases. It leverages a systematic review of existing literature and utilizes the GRADE methodology to formulate recommendations, enhancing the rigor of the guideline. The guideline appropriately acknowledges the limitations of the evidence base and identifies areas for future research. However, the lack of clear benefit for many outcomes, combined with the complexities of vitamin D metabolism and influence of various factors, highlights the need for nuanced interpretation of the findings.
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File Information
Original Title:
Vitamin D for the Prevention of Disease: An Endocrine Society Clinical Practice Guideline
Uploaded:
July 31, 2025 at 12:26 PM
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