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COSMETIC PLATELET-RICH PLASMA  ADVERTISMENT AS WRINKLE REJUVENATOR IS MISLEADING

Cape Town Thursday, 9 April 2009: Cosmetic and Beauty News.PRP fact or fiction?

A 12-month outcome- based, independent watchdog study, indicate that there is no firm scientific evidence that best-selling or revolutionary platelet-rich plasma (PRP), with or without cultured living cells, compared to cosmetic creams, can reduce wrinkles, lift or rejuvenate the face.  All ads from beauty and cosmetic laboratories are misleading, and the latest blow to the reputation of claims regarding PRP offering the elixir of youth. The ads are not supported by “robust science”, have contributed to failures, and that the sales pitch is not endorsed by independent Biomed Rated Scientists in Cape Town. The claims that PRP can give a middle-aged women young-looking skin is false and that most methodologies are flawed, either by poor objective measures and research been carried out by manufacturer employees or designates. The earlier 3 month results, claiming measurable rejuvenation have not held up and that PRP is far less effective than, peels, Botox or conventional fillers. PRP for plasma or “facial resurfacing” with your own cells does not produce a permanent lift or convincing rejuvenation/regeneration.  Independent graders show that skin sagging after intended PRP-facial rejuvenation with your own plasma, or mixed with cultured fibroblasts, is no better than placebo creams, regarding the face and neck. The earlier reports from UK and Japanese aesthetic units, utilizing new generation or revolutionary  PRP, could not be substantiated locally, using highly sophisticated measuring skin-analysis devices. At best, the beauty results are very modest and temporary, necessitating ad-on’s  to combat ongoing aging, as soon as 3-months after PRP-enhancement. Twelve-months results are a bridge too far and not realistic or backed by proper clinical trials or scientific publications.

The down-side of facial dermal injections with platelet-rich plasma (PRP) has been unsuspected severe and acute cutaneous anaphylaxis following injections near the eye, thus ruling out safety of PRP-mesotherapy of wrinkles under the eye. Reactions are supposedly due to the blood separator and anti-coagulant compounds in the collection tubes. Cavernous sinus thrombosis has been seen after rapid absorption of activated plasma and platelets in PRP, via the eye-cavity. The mitogenic pathways of growth factors in the skin dermis seen after activation of human platelets in PRP, may interact with growth promoters of human breast cancer cells. These include transforming growth factor-alpha and platelet-derived growth factor, found in enriched PRP used for cosmetic reasons. The incidence of breast cancer in women world-wide is 1 in 8, and 75% occur above the age of 50. In such persons absorption of GF over 10 hours, from cosmetic PRP factor-release, may be of great concern and therefore rules out safe needle-induced, PRP-mesotherapy of a women’s neck, décolleté or breast area. For the moment, attempts at dermal rejuvenation and regeneration with A-PRP by biological injection techniques should be discouraged in the peri-orbital, neck, décolleté or breast areas of pre-and post menopausal women who may be at risk. Such skin rejuvenation techniques should urgently be discontinued in any person who has had or received treatment for a growth. Time is needed to assess if super-concentrated autologous platelet-rich gels, given as dermal pulse-therapy in the facial and décolleté for rejuvenation, does not induce remote growths. Growth factors, cause cells to divide more rapidly, and are associated with tumour growth. For instance, recombinant forms of human platelet-derived growth factor cannot be used in persons with a history of skin cancer. Use thereof has been associated with a higher risk and incidence of variable remote tumours, and cancer deaths, than control population. For the moment, and for the above risks, Platelet Rich Gels, Lysates or Plasma, cannot be supported for facial anti-wrinkle or anti-aging rejuvenation therapy in the beauty industry, and until further, prospective clinical trials are urgently completed. A role is identifiable in clinical therapeutic medicine to enhance wound healing in selected persons.

"Device design and separator propriety may clearly explain successes and failures in the clinic, regarding rejuvenation capability, as well as cell stimulation.The various devices seem to induce slightly different end-products with differing biological GF-activity and potential uses.Platelet content and enrichment, varying types of platelet activators, leucocyte and fibrin content, centrifugation methodology, cell separators used, as well as growth factor variability and release-speed, play important roles in optimal PRP generation and ultimate biological effect seen in the clinic. Some of the devices now commercially available include: Regen, Plateltex, SmartPrep, Mycells, PCCS, Magellan or GPS PRP, Fibrinet, Choukroun's PRF ( contains thrombospondin-1: see Growth Factors, 2009), Vivostat PRF, Cell Separator PRP ( Ehrenfest D., et al :  Classification of platelet concentrates: Trends Biotechnology , 2009) ".

Figure: PRP can enhance and support cell growth ex-vivo with conventional culture mediums. PRP dermal rejuvenation in man is  not supported histologically by permanent regeneration of fibroblasts and incorporation of collagen and elastin ( x 8,000).

 

REFERENCES:

  1. Kumar V. Robbin’s Basic Pathology. 8th Edition, Saunders, 2007.
  2. Wang H. Platelet Rich Plasma: Myth or Reality. Eur J Dent 1(4):192-194 ( University of Michigan)

POSTED: 9 APRIL 2009 AND THE CONTENTS HAS BEEN REVIEWED BY A BIOMED-RATED SCIENTIST AND CLINICIAN FOR ACCURACY.

Table-1: COSMETIC/AESTHETIC PRP-UPDATE 2010. BIOMEDICAL SCIENCE , CLINICAL AND BASIC SCIENCES REGARDING PLATELET-RICH PLASMA (PRP): After Marx 2005 et al.

  • PRP releases seven growth-factors (GF) from activated platelets: these GF promote healing and regeneration ( tissue healing and biocellular regeneration).Thus, the GF are relevant to wound-healing
  • PRP is autogenous blood clot and contains concentrated numbers of platelets ( about 4-7 times baseline is needed for clinical benefit)
  • The alpha-granules of the platelet store the GF (PDGF, TGF,VEGF,EGF): GF are proteins and need to be biologically active to work: biological actions: stimulate mesenchymal stem cells and resident adult cells to replicate, osteoblast replication, endothelial cell-replication, fibroblast and osteoblast-replication to produce collagen, enhance bone-regeneration, stimulate matrix-formation, stimulation of pericytes, epidermal-regeneration and re-surfacing
  • PRP is not stem-cell therapy, but is non-invasive and fairly safe
  • PRP does not contain stem cells of any relevance, but may be directed at resident stem cells that are up-regulated after injection to replicate together with other mesenchymal cells
  • The platelet alpha-granules also contain cell-adhesion molecules and involved with vitronectin, fibronectin, fibrin
  • The GF have two active sites each and are called dimers
  • PRP: 94% platelets, 5% RBC, 1% WBC and no stem cells of note
  • Enhancement of autogenous bone-grafts used in maxilla-facial surgery and orthopaedics
  • PRP can be  considered for facial-regeneration /rejuvenation but the effects only last for 6-months and other complimentary treatments such as RF are needed to back-up or bolster the plasma. Stand-alone PRP-treatment is insufficient to reverse or ameliorate ageing and add-ons are needed
  • Enhanced proliferation of skin basal cells ( stem cells of the epithelium): following blood-clot formation (improved donor-site healing  after skin-graft)
  • Enhancement of osteointegration ( relevant to implant-surgery)
  • NB: Poor technique can render poor quality and PRP enrichment: one needs to concentrate viable bioactive platelets. Therefore the best PRP processing device is needed.
  • PRP can be used during stem cell transplantation and the biological action is referred to as: PROLIFERATION-PROMOTING EFFECT (may be used with human adipose-derived stem cells and human dermal-fibroblasts: see Kakudo et al,  Plast Reconstruct Surg 2008: 1352-60). Therefore PRP application can be utilised for cell-based, soft-tissue engineering and wound-healing
  • The topical efficacy, and level - evidence, has been demonstrated in the treatment of diabetic-foot ulceration. Numerous indications for PRP are described in cranio-facial surgery:  bone grafting, rhytidectomy, face-lift, fat-grafting and transfer
  • Potent cell proliferation enhancer ex vivo using fibroblasts, adipose-derived stem cells, keratinocytes
  • Controversial areas: PRP-MESOTHERAPY for facial rejuvenation and repair of solar-aged changes, sagging, wrinkling. The problems include unpredictable inconsistency, poor and no-response in some clients. It is an international experience. This is a feature of biologicals and applies to stem cell application at the time of posting. Need for additional facial back-up RF treatment is mandatory after PRP-MESOTHERAPY to reach benchmark cosmetic-output. Is it not the RF that is working or the PRP? For the moment cosmetic-scientists are not sure if subdermal and subcutaneous injections of PRP are superior to other established cosmetic treatments. Established cosmetic clinics have demonstrated that PRP-FACELIFT is not superior to superficial chemical-peel plus LED, IPL or fractionated laser. BOTOX and fillers are far superior to PRP in gaining quick results. PRP- mesotherapy is far more costly than BOTOX or DYSPORT. PRP is not stem cell therapy and cannot turn back the ageing clock completely. More robust science and evidence is needed. But it seems that PRP may well have a place in the cosmetic armamentarium of the cosmetic surgeon, dermatologist and aesthetic physician. PRP is more established in therapeutics at the clinic but not in the beauty salon.
  • Dermatological or plastic surgery consultation. Such a consultation is essential to assess if you are a suitable client for such treatment
  • References: Marx and Garg 2005, Quintessence; Kumar et al, Robbin’s Basic Pathology, 2007, 8th Edition, International Edition; Du Toit et al, The Specialist Forum 2007:7; 30-31.
  • PRODUCTS AVAILABLE IN RSARegen-PRP® (REGENKIT®) (Cost: R800 per tube); MyCells® (Neokit®) (costs: R1300 per tube).PRP-mesotherapy demonstration of technique is available on the Internet: See U-Tube demos by various doctors.
  • DISCLAIMER: This site provides no medical or cosmetic advice or recommendation and therefore an aesthetic expert should be consulted regarding any facial treatment, treatment choices to the neck, décolleté or dorsal aspects of the hands.
  • Formulation: BIOMED Expert and Specialist.
  • WEBSITE UPGRADING AND UPDATING: 16 November 2009. See BOLAND CELL menu: PRP UPDATE 2010.

 

 

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Boland Cell - Cell Technology - Aesthetic Biotechnology