A Comprehensive Systematic Review of Dynamic Nutrient Profiling for Personalized Diet Planning: Meta-Analysis and PRISMA-Based Evidence Synthesis
Abstract
1. Introduction
1.1. Background and Rationale
1.2. Evolution of Nutrient Profiling Systems
1.3. Clinical and Public Health Significance
1.4. Current Challenges and Knowledge Gaps
1.5. Research Objectives and Hypotheses
- What are the current methodological approaches for dynamic nutrient profiling, and how do they compare in terms of effectiveness and feasibility?
- What is the evidence for clinical and behavioral outcomes associated with personalized diet planning based on dynamic profiling?
- What factors contribute to the heterogeneity observed across studies, and how do they influence the interpretation of results?
- What are the current limitations and future research priorities for advancing the field?
- Our primary hypothesis is that dynamic nutrient profiling systems will demonstrate superior effectiveness compared to static approaches across multiple outcome domains, including dietary quality, adherence, and clinical markers. We further hypothesize that AI-enhanced systems and those incorporating multiple data streams will show greater effectiveness than simpler algorithmic approaches.
2. Methods
2.1. Protocol Development and Registration
2.2. Comprehensive Search Strategy
- PubMed/MEDLINE (1946 to December 2024)
- Scopus (1960 to December 2024)
- Web of Science Core Collection (1900 to December 2024)
- IEEE Xplore Digital Library (1963 to December 2024)
- Google Scholar (first 200 most relevant results)
- Cochrane Central Register of Controlled Trials (CENTRAL)
- ClinicalTrials.gov for ongoing and completed trials
2.3. Detailed Eligibility Criteria
2.3.1. Inclusion Criteria
2.3.2. Exclusion Criteria
- Conference abstracts, editorials, commentaries, or opinion pieces
- Studies focusing exclusively on static nutrient profiling without dynamic or personalized components
- Animal studies without direct human relevance
- Case reports or case series with fewer than 10 participants
- Studies not available in English
- Duplicate publications or multiple reports of the same study
- Studies with inadequate methodological detail to assess quality
2.4. Study Selection Process
2.5. Study Characteristics and Demographics
| Study Characteristic | n | Percentage (%) |
|---|---|---|
| Study Design | ||
| Randomized Controlled Trials | 34 | 29.1 |
| Cross-sectional Studies | 28 | 23.9 |
| Longitudinal Cohort Studies | 21 | 17.9 |
| Validation Studies | 18 | 15.4 |
| Systematic Reviews/Meta-analyses | 16 | 13.7 |
| Geographic Distribution | ||
| North America | 42 | 35.9 |
| Europe | 38 | 32.5 |
| Asia | 24 | 20.5 |
| Other regions | 13 | 11.1 |
| Population Focus | ||
| General adult population | 67 | 57.3 |
| Clinical populations | 28 | 23.9 |
| Athletes/active individuals | 12 | 10.3 |
| Pediatric populations | 10 | 8.5 |
| Sample Size Categories | ||
| <100 participants | 43 | 36.8 |
| 100–500 participants | 38 | 32.5 |
| 500–1000 participants | 21 | 17.9 |
| >1000 participants | 15 | 12.8 |
| Intervention Duration | ||
| <1 month | 18 | 15.4 |
| 1–3 months | 45 | 38.5 |
| 3–6 months | 32 | 27.4 |
| >6 months | 22 | 18.8 |
| Primary Outcomes | ||
| Dietary quality measures | 89 | 76.1 |
| Clinical biomarkers | 67 | 57.3 |
| Anthropometric measures | 54 | 46.2 |
| Behavioral outcomes | 43 | 36.8 |
2.6. Data Extraction and Management
- Author, year, country, study design
- Sample size, participant demographics
- Setting, duration of intervention/follow-up
- Funding sources and conflicts of interest
- Age, sex, health status
- Baseline nutritional status
- Comorbidities and medications
- Socioeconomic and demographic factors
- Type of dynamic profiling system
- Data inputs and measurement methods
- Algorithm or analytical approach
- Frequency of assessment and recommendation updates
- Delivery method and user interface
- Primary and secondary endpoints
- Measurement methods and timing
- Statistical analysis approaches
- Effect sizes and confidence intervals
2.7. Quality Assessment
2.8. Statistical Analysis and Meta-Analysis
- Type of dynamic profiling system
- Population characteristics (age, health status)
- Intervention duration
- Study quality
3. Results
3.1. Study Selection and Flow
3.2. Methodological Categories of Dynamic Profiling Systems
3.2.1. Algorithmic-Based Profiling Systems
- Traditional Algorithm Modifications: Many studies built upon established nutrient profiling systems such as the Nutrient Rich Food (NRF) index, adapting them for personalized applications [57,58,59,60]. Common modifications included individual weighting of nutrients based on personal health goals, demographic characteristics, or biomarker profiles.
- Multi-Criteria Decision Analysis: Advanced algorithmic approaches employed multi-criteria decision analysis techniques, such as the Analytic Hierarchy Process (AHP) enhanced with particle swarm optimization, to balance multiple competing nutritional objectives while accounting for individual preferences and constraints.
3.2.2. Biomarker-Integrated Approaches
- Metabolomic Profiling: Advanced approaches incorporated metabolomic analysis to identify metabolic phenotypes and predict individual responses to dietary interventions [76,77,78]. These systems could identify unique metabolic signatures associated with optimal dietary patterns for specific individuals.
3.2.3. AI-Enhanced Personalized Nutrition Platforms
- Natural Language Processing: Advanced systems incorporated natural language processing to analyze dietary records, food logs, and user preferences expressed in natural language, enabling more intuitive user interfaces and comprehensive data capture.
3.3. Technology Integration and Implementation
3.3.1. Data Input Methods
3.3.2. Technology Platform Usage
3.3.3. Quality Considerations and Future Standards
3.4. Meta-Analysis Results
3.4.1. Primary Outcomes: Dietary Quality and Nutrient Density
3.4.2. Secondary Outcomes: Clinical and Anthropometric Measures
- Weight Management: Fifteen studies reported weight change as an outcome. Meta-analysis revealed a significant reduction in body weight favoring dynamic profiling interventions (MD = −2.8 kg, 95% CI: −4.2 to −1.4, p < 0.001). While statistically significant, the clinical relevance of this reduction should be interpreted cautiously—a weight change of approximately 2–3 kg is modest and may contribute to metabolic improvements but is unlikely to achieve standalone therapeutic goals in obesity management without complementary lifestyle interventions.
- Cardiovascular Risk Markers: Twenty-three studies reported changes in cardiovascular markers. Significant improvements were observed for total cholesterol (MD = −12.4 mg/dL, 95% CI: −18.1 to −6.7, p < 0.001) and LDL-C (MD = −8.9 mg/dL, 95% CI: −13.4 to −4.5, p < 0.001). Although these reductions are moderate, they are clinically meaningful when sustained over time and could translate into a measurable reduction in cardiovascular risk.
- Glycemic Control: Among participants with diabetes or prediabetes (n = 12 studies), significant improvements were observed in HbA1c levels (MD = −0.31%, 95% CI: −0.46 to −0.16, p < 0.001). A reduction of ~0.3% is generally associated with a 10–15% relative reduction in microvascular complication risk, indicating that dynamic nutrient profiling may have clinically meaningful benefits in glycemic regulation when integrated into comprehensive care strategies.
3.4.3. Meta-Regression Analysis
3.5. Behavioral Outcomes and Adherence
3.5.1. Dietary Adherence
3.5.2. User Engagement and Satisfaction
3.6. Subgroup Analyses
3.6.1. Analysis by Profiling System Type
3.6.2. Analysis by Population Characteristics
3.7. Cost-Effectiveness Analysis
3.8. Publication Bias Assessment
3.9. Quality Assessment Results
3.10. Sensitivity Analysis
- Exclusion of High-Risk-of-Bias Studies: Analyses were repeated after excluding studies with high risk of bias based on quality assessment criteria. Results remained consistent (SMD = 1.21, 95% CI: 0.88–1.54) compared to the main analysis, indicating that the pooled effects were not disproportionately influenced by lower-quality studies.
- Alternative Effect Size Models: Both fixed-effects and random-effects models were applied. Effect sizes remained significant under both approaches (SMD range: 1.15–1.28), confirming that findings were not sensitive to the choice of model.
- Exclusion of Outliers: Outlier studies with effect sizes exceeding ±2 standard deviations from the mean were excluded to test their influence on overall results. The pooled effect size remained significant (SMD = 1.20, 95% CI: 0.86–1.53), indicating robustness against individual influential studies.
- Short vs. Long Follow-Up: Separate sensitivity analyses were conducted for studies with follow-up periods shorter than 3 months and those exceeding 6 months. Both subgroups maintained significant effects (SMD = 1.18 and 1.22, respectively), although slightly higher variability was observed in short-term studies.
4. Discussion
4.1. Principal Findings and Clinical Implications
4.2. Methodological Heterogeneity and System Evolution
4.3. Population-Specific Considerations
4.4. Technology Integration and Implementation Challenges
4.5. Economic and Public Health Implications
4.6. Limitations and Methodological Considerations
4.7. Future Research Directions and Priorities
4.7.1. Methodological Standardization
- Core outcome measures for evaluating profiling system effectiveness
- Standardized protocols for biomarker assessment and interpretation
- Validation frameworks for artificial intelligence algorithms
- Quality metrics for different profiling approaches
4.7.2. Long-Term Validation Studies
- Follow-up periods of at least 12 months
- Hard clinical endpoints (cardiovascular events, diabetes incidence)
- Cost-effectiveness analyses
- Assessment of long-term user engagement and adherence
4.7.3. Technology Development and Integration
- Development of more accurate and accessible biomarker assessment tools
- Integration of multi-omics data (genomics, metabolomics, microbiome)
- Improvement of user interface design and engagement strategies
- Development of interoperable systems for healthcare integration
4.7.4. Implementation Science Research
- Healthcare provider training and workflow integration studies
- Assessment of regulatory and policy barriers
- Investigation of optimal business models for sustainable implementation
- Evaluation of population-level implementation strategies
4.8. Clinical Practice Implications
5. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
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| System Type | Studies | SMD | 95% CI | p-Value | I2 |
|---|---|---|---|---|---|
| AI-Enhanced Systems | 8 | 1.67 | 1.23–2.11 | <0.001 | 72% |
| Biomarker-Integrated | 12 | 1.15 | 0.82–1.48 | <0.001 | 79% |
| Algorithmic-Based | 18 | 1.08 | 0.78–1.38 | <0.001 | 68% |
| Hybrid Approaches | 6 | 1.45 | 0.95–1.95 | <0.001 | 85% |
| Overall | 44 | 1.24 | 0.89–1.59 | <0.001 | 84% |
| Study Type | High Quality | Moderate Quality | Low Quality | Total |
|---|---|---|---|---|
| RCTs (n = 34) | 18 (52.9%) | 12 (35.3%) | 4 (11.8%) | 34 (100%) |
| Cohort Studies (n = 21) | 11 (52.4%) | 8 (38.1%) | 2 (9.5%) | 21 (100%) |
| Cross-sectional (n = 28) | 12 (42.9%) | 13 (46.4%) | 3 (10.7%) | 28 (100%) |
| Validation Studies (n = 18) | 14 (77.8%) | 3 (16.7%) | 1 (5.6%) | 18 (100%) |
| Systematic Reviews (n = 16) | 9 (56.3%) | 6 (37.5%) | 1 (6.3%) | 16 (100%) |
| Overall | 64 (54.7%) | 42 (35.9%) | 11 (9.4%) | 117 (100%) |
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© 2025 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
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Molooy Zada, M.H.; Pan, D.; Sun, G. A Comprehensive Systematic Review of Dynamic Nutrient Profiling for Personalized Diet Planning: Meta-Analysis and PRISMA-Based Evidence Synthesis. Foods 2025, 14, 3625. https://doi.org/10.3390/foods14213625
Molooy Zada MH, Pan D, Sun G. A Comprehensive Systematic Review of Dynamic Nutrient Profiling for Personalized Diet Planning: Meta-Analysis and PRISMA-Based Evidence Synthesis. Foods. 2025; 14(21):3625. https://doi.org/10.3390/foods14213625
Chicago/Turabian StyleMolooy Zada, Mohammad Hasan, Da Pan, and Guiju Sun. 2025. "A Comprehensive Systematic Review of Dynamic Nutrient Profiling for Personalized Diet Planning: Meta-Analysis and PRISMA-Based Evidence Synthesis" Foods 14, no. 21: 3625. https://doi.org/10.3390/foods14213625
APA StyleMolooy Zada, M. H., Pan, D., & Sun, G. (2025). A Comprehensive Systematic Review of Dynamic Nutrient Profiling for Personalized Diet Planning: Meta-Analysis and PRISMA-Based Evidence Synthesis. Foods, 14(21), 3625. https://doi.org/10.3390/foods14213625

