PMID- 38477463 OWN - NLM STAT- Publisher LR - 20240313 IS - 1945-7197 (Electronic) IS - 0021-972X (Linking) DP - 2024 Mar 13 TI - Improving Diabetic Wound Healing Outcomes with Topical Growth Factor Therapies: Systematic Review and Network Meta-analysis of Randomised-controlled Trials. LID - dgae128 [pii] LID - 10.1210/clinem/dgae128 [doi] AB - CONTEXT: Diabetes mellitus is associated with morbid complications such as diabetic foot ulcers (DFUs) that may lead to amputations or mortality if not managed adequately. OBJECTIVE: New adjunctive interventions to treat diabetic wounds include topical biologics and growth factors. This study aims to evaluate their efficacy in improving wound healing outcomes and safety. DATA SOURCES: Comprehensive database searches of MEDLINE via PubMed, EMBASE and Cochrane performed from inception to December 2022. STUDY SELECTION: Three independent researchers selected the studies. Randomised-controlled trials that compared the use of a topical biologic growth factor-containing regimen to other biologics or standard of care (SOC) were included. DATA EXTRACTION AND SYNTHESIS: This review followed PRISMA guidelines. Risk of bias analysis was performed using the Jadad scale. Network meta-analysis was performed. Treatments were grouped into common nodes based on the type of biologic agent. MAIN OUTCOMES AND MEASURES: Primary outcomes of interest were healing rate and time to wound closure. Secondary outcomes included wound infection, serious adverse events, and amputation rate. RESULTS: Human umbilical cord (HUC) was associated with the highest cure, followed by recombinant human epidermal growth factor (hEGF). A significantly greater reduction in the time to cure DFUs was seen in HUC, hEGF and fibroblast growth factor (FGF). There was a significantly lower risk of adverse events (AEs) when platelet-rich plasma (PRP) was administered. CONCLUSION: HUC, hEGF and FGF are promising topical biologics with statistically significant primary outcomes compared to SOC, while PRP is effective in reducing ulcer-related AEs. HUC has been found to be the most effective in terms of cure rate and a reduction in time to cure. CI - (c) The Author(s) 2024. Published by Oxford University Press on behalf of the Endocrine Society. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site-for further information please contact journals.permissions@oup.com. FAU - Wong, Andrew Yew Wei AU - Wong AYW AUID- ORCID: 0009-0008-8667-0334 AD - Yong Loo Lin School of Medicine, National University of Singapore, Singapore. FAU - Hooi, Natalie Ming Foong AU - Hooi NMF AD - Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore. FAU - Yeo, Brian Sheng Yep AU - Yeo BSY AD - Yong Loo Lin School of Medicine, National University of Singapore, Singapore. FAU - Sultana, Rehena AU - Sultana R AD - Duke-NUS Medical School, National University of Singapore, Singapore. FAU - Bee, Yong Mong AU - Bee YM AD - Department of Endocrinology, Singapore General Hospital, Singapore. FAU - Lee, Ainsley Ryan Yan Bin AU - Lee ARYB AUID- ORCID: 0000-0002-5896-2929 AD - Yong Loo Lin School of Medicine, National University of Singapore, Singapore. FAU - Tay, Sook Muay AU - Tay SM AUID- ORCID: 0000-0001-8028-9470 AD - Yong Loo Lin School of Medicine, National University of Singapore, Singapore. AD - Department of Surgical Intensive Care, Singapore General Hospital, Singapore. LA - eng PT - Journal Article DEP - 20240313 PL - United States TA - J Clin Endocrinol Metab JT - The Journal of clinical endocrinology and metabolism JID - 0375362 SB - IM OTO - NOTNLM OT - Diabetes Complications OT - Diabetes mellitus OT - Diabetic foot OT - Diabetic neuropathies OT - Diabetic ulcers OT - Wound healing EDAT- 2024/03/13 12:47 MHDA- 2024/03/13 12:47 CRDT- 2024/03/13 08:14 PHST- 2023/11/17 00:00 [received] PHST- 2024/02/28 00:00 [revised] PHST- 2024/02/29 00:00 [accepted] PHST- 2024/03/13 12:47 [medline] PHST- 2024/03/13 12:47 [pubmed] PHST- 2024/03/13 08:14 [entrez] AID - 7627888 [pii] AID - 10.1210/clinem/dgae128 [doi] PST - aheadofprint SO - J Clin Endocrinol Metab. 2024 Mar 13:dgae128. doi: 10.1210/clinem/dgae128.