PMID- 35273056 OWN - NLM STAT- MEDLINE DCOM- 20220427 LR - 20221207 IS - 2044-6055 (Electronic) IS - 2044-6055 (Linking) VI - 12 IP - 3 DP - 2022 Mar 10 TI - Short-term effectiveness of nutrition therapy to treat type 2 diabetes in low-income and middle-income countries: systematic review and meta-analysis of randomised controlled trials. PG - e056108 LID - 10.1136/bmjopen-2021-056108 [doi] LID - e056108 AB - OBJECTIVES: This review examined the evidence arising from randomised controlled trials regarding the impact of nutrition therapy on glycaemic control in people living with type 2 diabetes mellitus (T2DM) in low/middle-income countries (LMICs). DESIGN: Systematic review and meta-analysis using the Grading of Recommendations, Assessment, Development and Evaluation (GRADE) Approach. DATA SOURCES: MEDLINE, EMBASE, Web of Science, OpenGrey and the International Clinical Trials Registry were searched (up to July 3 2020). ELIGIBILITY CRITERIA: Trials were included if they evaluated nutrition therapy in adults diagnosed with T2DM, were conducted in LMICs, measured glycaemic control and the trial included a 3-month post-intervention assessment. Nutrition therapy was defined according to American Diabetes Association recommendations. DATA EXTRACTION AND SYNTHESIS: Two independent reviewers screened the database. Study characteristics and outcome data were extracted using a data collection form. Meta-analyses were conducted for glycated haemoglobin (HbA1c) and fasting blood glucose. Trials were assessed for risk of bias (Cochrane Risk-of-Bias, Version 2.0) and overall certainty of evidence (GRADE). RESULTS: Four trials met inclusion criteria (total n=463), conducted in Malaysia, Iran and South Africa. All trials focused on nutrition education with no direct prescription or manipulation of diet. Mean differences between intervention and standard care were -0.63% (95% CI -1.47% to 0.21%) for HbA1c and -13.63 mg/dL (95% CI -37.61 to 10.34) for fasting blood glucose in favour of the intervention. Given the small number of eligible trials, moderate to high risk of publication bias and serious concerns regarding consistency and precision of the evidence, certainty of evidence was deemed to be very low. CONCLUSIONS: There is a lack of well-conducted randomised controlled trials that examine the long-term impact of nutrition therapy in LMICs, preventing firm conclusions to be made on their effectiveness. Further research is essential to discover realistic, evidence-based solutions. PROSPERO REGISTRATION NUMBER: CRD42020188435. CI - (c) Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY. Published by BMJ. FAU - Guilbert, Elizabeth AU - Guilbert E AD - Faculty of Health Sciences, University of Bristol, Bristol, UK. FAU - Perry, Rachel AU - Perry R AUID- ORCID: 0000-0001-5874-3016 AD - National Institute for Health Research Bristol Biomedical Research Centre; University Hospitals of Bristol and Weston NHS Foundation Trust and University of Bristol, Bristol, UK. FAU - Whitmarsh, Alex AU - Whitmarsh A AD - National Institute for Health Research Bristol Biomedical Research Centre; University Hospitals of Bristol and Weston NHS Foundation Trust and University of Bristol, Bristol, UK. FAU - Sauchelli, Sarah AU - Sauchelli S AUID- ORCID: 0000-0003-3620-7671 AD - National Institute for Health Research Bristol Biomedical Research Centre; University Hospitals of Bristol and Weston NHS Foundation Trust and University of Bristol, Bristol, UK sarah.sauchellitoran@bristol.ac.uk. LA - eng PT - Journal Article PT - Meta-Analysis PT - Research Support, Non-U.S. Gov't PT - Systematic Review DEP - 20220310 PL - England TA - BMJ Open JT - BMJ open JID - 101552874 RN - 0 (Blood Glucose) RN - 0 (Glycated Hemoglobin A) SB - IM MH - Adult MH - Blood Glucose MH - Developing Countries MH - *Diabetes Mellitus, Type 2 MH - Glycated Hemoglobin MH - Humans MH - *Nutrition Therapy MH - Randomized Controlled Trials as Topic PMC - PMC8915303 OTO - NOTNLM OT - general diabetes OT - nutrition & dietetics OT - public health COIS- Competing interests: None declared. EDAT- 2022/03/12 06:00 MHDA- 2022/04/28 06:00 PMCR- 2022/03/10 CRDT- 2022/03/11 05:36 PHST- 2022/03/11 05:36 [entrez] PHST- 2022/03/12 06:00 [pubmed] PHST- 2022/04/28 06:00 [medline] PHST- 2022/03/10 00:00 [pmc-release] AID - bmjopen-2021-056108 [pii] AID - 10.1136/bmjopen-2021-056108 [doi] PST - epublish SO - BMJ Open. 2022 Mar 10;12(3):e056108. doi: 10.1136/bmjopen-2021-056108.