| Literature DB >> 28331983 |
Setor K Kunutsor1, Jari A Laukkanen2,3, Michael R Whitehouse4, Ashley W Blom4.
Abstract
PURPOSE: The Mediterranean diet is associated with decreased morbidity and mortality from various chronic diseases. Adherence to a Mediterranean-style diet has been suggested to have protective effects on bone health and decreases the incidence of bone fractures, but the evidence is not clear. We conducted a systematic review and meta-analysis of available observational studies to quantify the association between adherence to a Mediterranean-style diet, as assessed by the Mediterranean Diet Score (MDS), and the risk of fractures in the general population.Entities:
Keywords: Bone; Fractures; Mediterranean diet; Nutrition
Mesh:
Year: 2017 PMID: 28331983 PMCID: PMC5959988 DOI: 10.1007/s00394-017-1432-0
Source DB: PubMed Journal: Eur J Nutr ISSN: 1436-6207 Impact factor: 5.614
Characteristics of published observational studies evaluating associations between adherence to a Mediterranean-style diet and incident fractures
| Lead author, publication year [Reference] | Name of study or source of participants | Location of study | Year(s) of baseline survey | Baseline mean age (age range), years | % male | Mean or median duration of follow-up (years) | Total no. of participants | No. of cases | Primary outcome | Other bone health outcomes | Covariates adjusted for | Exposure | Mean (SD) or median (range) for MDS |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Benetou, 2013 [ | EPIC | Multi-European | 1992–2000 | 48.6 (35–70) | 25.9 | 9.0.0 | 188,795 | 802 | Hip fractures | NA | Age, sex, education, smoking status, BMI, height, physical activity, total energy intake, history of diabetes, history of CVD, history of cancer, history of fracture, and country | Modified Mediterranean Diet Score | NR |
| Feart, 2013 [ | Three-City Study | France | 2001–2002 | 47.8 (≥67) | 37.1 | 8.0 | 1482 | 155 | Hip and any fractures (hip, vertebral, or wrist fractures) | NA | Age, gender, physical activity, total energy intake, additional adjustment for educational level, marital status, BMI, self-reported osteoporosis, osteoporosis treatment, calcium and/or vitamin D treatment | Mediterranean Diet Score | 4.38 (1.68) |
| Zeng, 2014 [ | Hip fracture patients and community-sourced controls | China | 2009–2013 | 71.0 (55–80) | 24.4 | NA | 1452 | 726 | Hip fractures | NA | Age, BMI, education, marital status, occupation, household income, house orientation, smoking status, tea drinking, family history of fractures, calcium supplement user, multivitamin user, physical activity, and daily energy intake | Alternate Mediterranean Diet Score | 3 (0–7) in cases |
| Haring, 2016 [ | WHI Observational Study | USA | 1993–1998 | (50–79) | 0.0 | 15.9 | 90,014 | 28,718 | Hip and total fractures (all fractures except toe, finger, sternum, and clavicle fractures) | BMD and lean body mass index | Age, race/ethnicity, BMI, smoking status, physical activity, self-reported health, DM, history of fracture at 55 years or older, physical function score, number of chronic medical conditions, number of psychoactive medications, and use of hormone therapy, bisphosphonates, calcitonin, and selective estrogen receptor modulators | Alternate Mediterranean Diet Score | NR |
| Byberg, 2016 [ | COSM and SMC | Sweden | 1997 | 60.0 (NR) | 53.1 | 15.0 | 71,333 | 3175 | Hip fractures | NA | Age, sex, BMI, height, DM, smoking status, physical exercise, educational level, living alone, total energy intake, energy adjusted intake of calcium, vitamin D and retinol, use of supplements containing calcium or vitamin D, and Charlson’s weighted comorbidity index | Modified Mediterranean Diet Score | NR |
BMD bone mineral density, BMI body mass index, COSM Cohort of Swedish Men, CVD cardiovascular disease, DM diabetes mellitus, EPIC European Prospective Investigation into Cancer, MDS Mediterranean diet score, NA not applicable, NR not reported, SMC Swedish Mammography Cohort, WHI Womens Health Initiative
Fig. 1Association between adherence to a Mediterranean-style diet and risk of hip fractures in observational cohort studies. CI confidence interval (bars); RR relative risk; the RRs for fractures are per two-point increment in adherence to the Mediterranean Diet Score
| Section/topic | Item No | Checklist item | Reported on page No |
|---|---|---|---|
| Title | |||
| Title | 1 | Identify the report as a systematic review, meta-analysis, or both | Title |
| Abstract | |||
| Structured summary | 2 | Provide a structured summary including, as applicable, background, objectives, data sources, study eligibility criteria, participants, interventions, study appraisal, synthesis methods, results, limitations, conclusions and implications of key findings, and systematic review registration number | Introduction |
| Introduction | |||
| Rationale | 3 | Describe the rationale for the review in the context of what is already known | Introduction |
| Objectives | 4 | Provide an explicit statement of questions being addressed with reference to participants, interventions, comparisons, outcomes, and study design (PICOS) | Introduction |
| Methods | |||
| Protocol and registration | 5 | Indicate if a review protocol exists, if and where it can be accessed (such as web address), and, if available, provide registration information including registration number | Not applicable |
| Eligibility criteria | 6 | Specify study characteristics (such as PICOS and length of follow-up) and report characteristics (such as years considered, language, and publication status) used as criteria for eligibility, giving rationale | Methods |
| Information sources | 7 | Describe all information sources (such as databases with dates of coverage and contact with study authors to identify additional studies) in the search and date last searched | Methods |
| Search | 8 | Present full electronic search strategy for at least one database, including any limits used, such that it could be repeated | Appendix 3 |
| Study selection | 9 | State the process for selecting studies (that is, screening, eligibility, included in systematic review, and, if applicable, included in the meta-analysis) | Methods |
| Data collection process | 10 | Describe method of data extraction from reports (such as piloted forms, independently, in duplicate) and any processes for obtaining and confirming data from investigators | Methods |
| Data items | 11 | List and define all variables for which data were sought (such as PICOS and funding sources) and any assumptions and simplifications made | Methods |
| Risk of bias in individual studies | 12 | Describe methods used for assessing risk of bias of individual studies (including specification of whether this was done at the study or outcome level), and how this information is to be used in any data synthesis | Methods |
| Summary measures | 13 | State the principal summary measures (such as risk ratio and difference in means) | Methods |
| Synthesis of results | 14 | Describe the methods of handling data and combining results of studies, if done, including measures of consistency (such as I2 statistic) for each meta-analysis | Methods |
| Risk of bias across studies | 15 | Specify any assessment of risk of bias that may affect the cumulative evidence (such as publication bias and selective reporting within studies) | Methods |
| Additional analyses | 16 | Describe methods of additional analyses (such as sensitivity or subgroup analyses and meta-regression), if done, indicating which were pre-specified | Not applicable |
| Results | |||
| Study selection | 17 | Give numbers of studies screened, assessed for eligibility, and included in the review, with reasons for exclusions at each stage, ideally with a flow diagram | Results and Figure |
| Study characteristics | 18 | For each study, the present characteristics for which data were extracted (such as study size, PICOS, and follow-up period) and provide the citations | Table |
| Risk of bias within studies | 19 | Present data on risk of bias of each study and, if available, any outcome-level assessment (see item 12) | Table |
| Results of individual studies | 20 | For all outcomes considered (benefits or harms), present for each study (a) simple summary data for each intervention group and (b) effect estimates and confidence intervals, ideally with a forest plot | Figure |
| Synthesis of results | 21 | Present results of each meta-analysis done, including confidence intervals and measures of consistency | Figure |
| Risk of bias across studies | 22 | Present results of any assessment of risk of bias across studies (see item 15) | Not applicable |
| Additional analysis | 23 | Give results of additional analyses, if done (such as sensitivity or subgroup analyses, meta-regression) (see item 16) | Not applicable |
| Discussion | |||
| Summary of evidence | 24 | Summarize the main findings including the strength of evidence for each main outcome; consider their relevance to key groups (such as health care providers, users, and policy makers) | Discussion |
| Limitations | 25 | Discuss limitations at study and outcome level (such as risk of bias), and at review level (such as incomplete retrieval of identified research and reporting bias) | Discussion |
| Conclusions | 26 | Provide a general interpretation of the results in the context of other evidence and implications for future research | Discussion |
| Funding | |||
| Funding | 27 | Describe sources of funding for the systematic review and other support (such as supply of data) and role of funders for the systematic review | Discussion |
| Criteria | Brief description of how the criteria were handled in the review | |
|---|---|---|
| Reporting of background | ||
| √ | Problem definition | The Mediterranean diet is associated with decreased morbidity and mortality from various chronic diseases. Adherence to a Mediterranean-style diet has been suggested to have protective effects on bone health and decreases the incidence of bone fractures, but the evidence is not clear. We conducted a systematic review and meta-analysis of available observational studies to quantify the association between adherence to a Mediterranean-style diet, as assessed by the Mediterranean Diet Score (MDS), and the risk of fractures in the general population |
| √ | Hypothesis statement | Adherence to a Mediterranean-style diet is associated with decreased risk of fractures |
| √ | Description of study outcomes | Any fractures |
| √ | Type of exposure | Adherence to a Mediterranean-style diet |
| √ | Type of study designs used | Longitudinal studies (prospective or retrospective case–control, prospective cohort, retrospective cohort, case-cohort, nested case–control, or clinical trials) |
| √ | Study population | Participants based in general populations in whom adherence to a Mediterranean-style diet has been assessed and have been followed-up for fracture outcomes |
| Reporting of search strategy should include | ||
| √ | Qualifications of searchers | Setor Kunutsor, PhD; Jari Laukkanen, PhD |
| √ | Search strategy, including time period included in the synthesis and keywords | Time period: from inception to October, 2016 |
| √ | Databases and registries searched | MEDLINE, EMBASE, and Web of Science, and Cochrane databases |
| √ | Search software used, name and version, including special features | OvidSP was used to search EMBASE and MEDLINE |
| √ | Use of hand searching | We searched bibliographies of retrieved papers |
| √ | List of citations located and those excluded, including justifications | Details of the literature search process are outlined in the flow chart in Appendix 5 |
| √ | Method of addressing articles published in languages other than English | We placed no restrictions on language |
| √ | Method of handling abstracts and unpublished studies | Not applicable |
| √ | Description of any contact with authors | Not applicable |
| Reporting of methods should include | ||
| √ | Description of relevance or appropriateness of studies assembled for assessing the hypothesis to be tested | Detailed inclusion and exclusion criteria are described in the “ |
| √ | Rationale for the selection and coding of data | Data extracted from each of the studies were relevant to the population characteristics, study design, exposure, and outcome |
| √ | Assessment of confounding | We assessed confounding by ranking individual studies on the basis of different adjustment levels and performed subgroup analyses to evaluate differences in the overall estimates according to levels of adjustment |
| √ | Assessment of study quality, including blinding of quality assessors; stratification or regression on possible predictors of study results | Study quality was assessed based on the nine-star Newcastle–Ottawa Scale using pre-defined criteria namely: population representativeness, comparability (adjustment of confounders), ascertainment of outcome |
| √ | Assessment of heterogeneity | Heterogeneity of the studies was quantified with I2 statistic that provides the relative amount of variance of the summary effect due to the between-study heterogeneity and explored using meta-regression and stratified analyses |
| √ | Description of statistical methods in sufficient detail to be replicated | Description of methods of meta-analyses, sensitivity analyses, meta-regression, and assessment of publication bias are detailed in the methods. We performed random effects meta-analysis with Stata 14 |
| √ | Provision of appropriate tables and graphics | Table and Figure |
| Reporting of results should include | ||
| √ | Graph summarizing individual study estimates and overall estimate | Figure |
| √ | Table giving descriptive information for each study included | Table |
| √ | Results of sensitivity testing | Sensitivity analysis was conducted to assess the influence of some large studies and low-quality studies on the pooled estimate. This was done by omitting such studies and calculating a pooled estimate for the remainder of the studies |
| √ | Indication of statistical uncertainty of findings | 95% confidence intervals were presented with all summary estimates, I2 values and results of sensitivity analyses |
| Reporting of discussion should include | ||
| √ | Quantitative assessment of bias | Sensitivity analyses indicate heterogeneity in strengths of the association due to most common biases in observational studies. The systematic review is limited in scope, as it involves limited number of studies |
| √ | Justification for exclusion | All studies were excluded based on the pre-defined inclusion criteria in |
| √ | Assessment of quality of included studies | Brief discussion included in ‘Methods’ section |
| Reporting of conclusions should include | ||
| √ | Consideration of alternative explanations for observed results | Discussion |
| √ | Generalization of the conclusions | Discussed in the context of the results |
| √ | Guidelines for future research | We recommend well-designed observational studies as well as clinical trials |
| √ | Disclosure of funding source | Not applicable |
| References |
|---|
| Chêne, G and Thompson, SG. Methods for Summarizing the Risk Associations of Quantitative Variables in Epidemiologic Studies in a Consistent Form. American Journal of Epidemiology. 1996;144:610–621 |
| Greenland, S and Longnecker, MP. Methods for trend estimation from summarized dose–response data, with applications to meta-analysis. American Journal of Epidemiology. 1992;135:1301–1309 |
| Orsini N, Bellocco R, Greenland S. Generalized least squares for trend estimation of summarized dose–response data. Stata Journal. 2006; 6:40–57 |
| Kunutsor SK, Apekey TA, Walley J. Liver aminotransferases and risk of incident type 2 diabetes: a systematic review and meta-analysis. Am J Epidemiol. 2013; 178 (2): 159 − 17 |