Literature DB >> 34014340

The safety and efficacy of autologous adipose-derived stromal vascular fraction for nonscarring alopecia: A systematic review.

Bianca Y Kang1, Alvin W Li1, Ming H Lee1, Clarissa C Wong1, Noor Naseer1, Sarah A Ibrahim1, Corinne H Miller2, Emily L Keimig1, Emily Poon1, Murad Alam3,4,5,6.   

Abstract

IMPORTANCE: Nonscarring alopecia, including androgenetic alopecia and alopecia areata, are common and can negatively impact quality of life. Recent clinical studies have investigated autologous, adipose-derived stromal vascular fraction (SVF) as a potentially beneficial treatment option.
OBJECTIVE: To assess the available evidence on the utility and safety of SVF for nonscarring alopecia. EVIDENCE REVIEW: A systematic review of the literature was performed using MEDLINE (PubMed), Embase, and CENTRAL from inception to November 2020. Included articles were prospective, observational or interventional studies of SVF for nonscarring alopecia in humans.
FINDINGS: Six studies of 188 patients were identified, including three randomized controlled trials. There were no reported severe adverse events. All studies found improved hair density with SVF compared to control or pre-treatment baseline. One study reported that improvement in hair density varied based on time for follow-up, severity of hair loss, and concentration of adipose-derived stem cells (ADSCs) within the SVF. Two studies reported an increase in hair diameter from baseline, and two studies reported an improvement in hair pull test outcomes. CONCLUSIONS AND RELEVANCE: SVF may be safe and effective for nonscarring alopecia in the appropriate patients. Hair loss severity, method of SVF preparation and frequency of treatment, and adjunctive therapies may be important considerations for treatment success. Additional studies evaluating appropriate patient selection and treatment methods are needed.
© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  Autologous; Efficacy; Nonscarring alopecia; Safety; Stromal vascular fraction; Systematic review

Mesh:

Year:  2021        PMID: 34014340     DOI: 10.1007/s00403-021-02238-7

Source DB:  PubMed          Journal:  Arch Dermatol Res        ISSN: 0340-3696            Impact factor:   3.017


  5 in total

Review 1.  Alopecia areata and health-related quality of life: a systematic review and meta-analysis.

Authors:  F Rencz; L Gulácsi; M Péntek; N Wikonkál; P Baji; V Brodszky
Journal:  Br J Dermatol       Date:  2016-07-02       Impact factor: 9.302

2.  Stromal vascular fraction-enriched platelet-rich plasma therapy reverses the effects of androgenetic alopecia.

Authors:  Ghazala Butt; Ijaz Hussain; Fridoon Jawad Ahmad; Mahmood S Choudhery
Journal:  J Cosmet Dermatol       Date:  2019-09-21       Impact factor: 2.696

3.  Stromal cells from the adipose tissue-derived stromal vascular fraction and culture expanded adipose tissue-derived stromal/stem cells: a joint statement of the International Federation for Adipose Therapeutics and Science (IFATS) and the International Society for Cellular Therapy (ISCT).

Authors:  Philippe Bourin; Bruce A Bunnell; Louis Casteilla; Massimo Dominici; Adam J Katz; Keith L March; Heinz Redl; J Peter Rubin; Kotaro Yoshimura; Jeffrey M Gimble
Journal:  Cytotherapy       Date:  2013-04-06       Impact factor: 5.414

4.  Design characteristics, risk of bias, and reporting of randomised controlled trials supporting approvals of cancer drugs by European Medicines Agency, 2014-16: cross sectional analysis.

Authors:  Huseyin Naci; Courtney Davis; Jelena Savović; Julian P T Higgins; Jonathan A C Sterne; Bishal Gyawali; Xochitl Romo-Sandoval; Nicola Handley; Christopher M Booth
Journal:  BMJ       Date:  2019-09-18

5.  Cellular therapy with human autologous adipose-derived adult cells of stromal vascular fraction for alopecia areata.

Authors:  Rami Anderi; Nehman Makdissy; Albert Azar; Francine Rizk; Aline Hamade
Journal:  Stem Cell Res Ther       Date:  2018-05-15       Impact factor: 6.832

  5 in total

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