Authors
Ebraheem Albazee, Abdullah AlOtaibi, Husain Alsaffar, Fanr F Alraqum, Shouq Alkhatlan, Bader N Almutawaa, Hasan M Aziz
Published in
Aesthetic plastic surgery. Jun 21, 2026. Epub Jun 21, 2026.
Abstract
Atrophic acne scarring is a prevalent and psychologically distressing sequela of acne vulgaris, often resulting from insufficient matrix remodeling and collagen loss. While microneedling is a safe treatment, its efficacy as a monotherapy is often limited. Autologous platelet-rich plasma (PRP) is the current gold standard adjuvant, but its high cost and invasiveness restrict its use. Topical insulin has emerged as a cost-effective, non-invasive alternative to promote wound healing.
A comprehensive search was conducted across PubMed, Web of Science, CENTRAL, Scopus, and Google Scholar for comparative studies published up to January 2026. Risk of bias was assessed using the RoB-2 and ROBINS-I tools. The primary outcome was significant clinical improvement (>50%). Secondary outcomes included changes in scar severity scores and adverse events. Risk ratios (RRs) and standardized mean differences (SMDs) were pooled with 95% confidence intervals (CIs). Trial sequential analysis was also performed.
Five studies involving 256 patients were included. Microneedling with topical insulin was associated with a significantly higher rate of significant clinical improvement compared to PRP (RR = 1.96, 95% CI [1.30-2.95], p < 0.0001). However, the pooled analysis of changes in scar severity scores showed no significant difference between groups (SMD = - 0.52, 95% CI [- 1.44, 0.39], p = 0.26), with high heterogeneity. Regarding safety, there was no significant difference in the risk of post-inflammatory hyperpigmentation (RR = 0.72, 95% CI [0.14-3.62], p = 0.69), and no episodes of hypoglycemia were reported.
Microneedling with topical insulin may achieve a higher rate of significant clinical improvement than PRP, with a comparable safety profile. However, given the inconclusive trial sequential analysis, high heterogeneity, and low overall certainty of evidence, these findings should be interpreted with caution. Further adequately powered trials are required to confirm this preliminary signal.
This journal requires that authors assign a level of evidence to each submission to which Evidence-Based Medicine rankings are applicable. This excludes Review Articles, Book Reviews, and manuscripts that concern Basic Science, Animal Studies, Cadaver Studies, and Experimental Studies. For a full description of these Evidence-Based Medicine ratings, please refer to the Table of Contents or the online Instructions to Authors www.springer.com/00266 .
PMID:
42324392
Bibliographic data and abstract were imported from PubMed on 22 Jun 2026.
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