In recent years, the dietary supplement use has increased both in Europe and in the USA with many physicians recommending their use [
Different studies on dietary supplements are arising in the scientific literature confirming the efficacy of dietary supplementation on maintaining and improving skin, hairs, and nails conditions. In 2007, Jacquet et al. [
Cynatine HNS contains a protein called keratin, in a peptide form obtained by proprietary processing of New Zealand sheep wool. This novel ingredient is stable over a wide range of pH and under conditions of elevated temperature. Keratin protein is one of nature’s richest sources of cysteine. Based on this, we hypothesized that Cynatine HNS may act synergistically with the cells’ own antioxidant defense, boosting glutathione and other sulfur rich proteins and peptides. Keratin is the protein from which the majority of hair and nails are made.
This study was a single-center, randomized, parallel group, double-blind, placebo-controlled 90-day intervention study in 50 subjects with signs of damaged hair and nails conducted at a single site in Italy (Farcoderm, University of Pavia). This clinical research study was done in accordance with the ethical principles for medical research involving human subjects (Helsinki Declaration, revised in 1983) and was approved by the internal ethical committee (Rif. 1032-11-SB). Informed consent documents were signed by all participants after study details were explained and each participant was evaluated for inclusion and exclusion criteria evaluated by dermatologists in the screening phase. Inclusion criteria for the study included being female and being between 40 and 71 years old, Caucasian, clinical signs of stressed or damaged hair, and an agreement not to use other possible cosmetic treatments which could interfere with the study. Exclusion criteria included subjects who did not fit the inclusion criteria, pregnant or breastfeeding women, use of a similar product to the active, and metabolism disorders. Once the inclusion criteria were met and consent forms were received, a screening number was assigned and entered into a screening and enrollment log. A randomization number was then given to each subject and a nonblinded employee provided the blinded examiner with the correct product at the beginning of each treatment period.
Once subjects were enrolled in the study they were provided with a base shampoo and conditioner to standardize the cosmetic habits for evaluation of product effects on hair as well as instructions. They were asked to use the base shampoo for five days and to return for their baseline visit (Day 0). At baseline, the dermatologist rechecked compliance of subjects to the protocol, evaluated baseline value for endpoints to be measured, hair (pull test, anagen/telogen evaluation, amino acid composition, mechanical properties, and appearance) and nails (clinical evaluation for nail status and breakage tendency), and supplied subjects with either active or placebo capsules and other information needed. A daily diary was also maintained in order to evaluate the habits of the volunteers in regard to foods and drinks during the first two weeks of the study as well as tobacco habits. At the end of the study period a questionnaire was filled out regarding the participants’ personal opinion about the treatment (tolerability, acceptability, and efficacy). Subjects were asked to return to have the same endpoints for hair and nails measured at 30, 60, and 90 days.
The investigational product Cynatine HNS and placebo, provided by Roxlor Global, LLC, were given to the subjects as capsules packaged in blister packages. All Cynatine HNS capsules contained 250 mg Cynatine (keratin), 7.5 mg zinc, 9.0 mg vitamin B3, 0.825 mg copper, 6.84 mg vitamin B5, 1.0 mg vitamin B6, and 0.150 mg vitamin B8 (Biotin) on an active dose basis. Each placebo capsule, identical in size, shape, and color, contained the inactive ingredients maltodextrin 370 mg and magnesium stearate 5.0 mg. On Day 1, subjects were instructed to take two capsules daily in the morning after breakfast.
All subjects known to have started treatment and who returned to the clinic for at least one follow-up visit were included in the analyses. The Cynatine HNS group had one withdrawal after Day 30 giving an
The effects of both the active and placebo groups were measured on hair using five separate tests. These tests were a pull test, an anagen/telogen evaluation of the hair, the amino acid composition of the hair, the tensile strength of the hair, and the clinically evaluated appearance of the hair.
The pull test helps evaluate diffuse scalp hair loss. Gentle traction was exerted on a bunch of hairs (about 60) in three areas of the scalp (frontal, temporal, and occipital) and the number of extracted hairs was counted. The dermatologist takes a few strands between his/her thumb and forefinger and pulls them gently. In anagen phase, growing hair should remain rooted in place while hair in the telogen phase should come out easily. If the number of lost hairs is greater than 9, pull test is positive and suggestive of telogen effluvium. The subjects were asked to refrain from washing their hair 2-3 days before the pull test.
Anagen/telogen testing is performed by choosing a targeted area (mid-vertex) of approximately 1.8 cm2 for clipping hair, which was dyed for gray and fair colored hair. Close-up digital photographs were immediately taken after shaving and 2 days later. The two photographs were compared by software that was able to determine if hair was in anagen phase (growing) or telogen phase (not growing). For the amino acid composition of the hair, hair samples were hydrolyzed in 6 M HCl aqueous solution. Amino acids were then separated by reverse-phase liquid chromatography and identified in an X-LC fluorimeter (model 3020FP). The amino acids measured for this test are serine, glutamic acid, cystine, and methionine. The breakage force of a single hair fiber was evaluated by a dynamometer (Tensolab 2512A, Mesdan Lab). An average of 10 readings is reported.
The hair appearance is evaluated by a licensed dermatologist who assigns a value of one to three based upon the subject’s hair brightness and luster. A score of 1 is dull and devoid of brightness, a score of 2 is basically dull and not so bright, and a score of 3 is shiny and bright.
The nail appearance and tendency to break were evaluated by a licensed dermatologist. The appearance of the nails is recorded in 5 either/or categories. These categories are Hard/Soft, Resistant/Fragile, Broken/Not Broken, Rough/Smooth, and Yellowish/White. The nails tendency to break is evaluated on Day 0 with a score of one to three. A score of 1 indicates that nails are flaked, are broken, or have a tendency to break, a score of 2 means nails are moderately flaked, broken, and a score of 3 indicates that neither nails are flaked, broken nor do they have a tendency to break. At Days 30, 60, and 90, the nails tendency to break is measured via a four-point scale. A score of 1 is no improvement, 2 is slight improvement, 3 is moderate improvement, and 4 is remarkable improvement. For the nail tendency to break measures, a subject with a score of 3 initially is not included in the analysis as there is no room for improvement. Eight subjects on Cynatine HNS had scores of 3, which lowers the respective
To evaluate the fact that the statistical analysis was accurate and reliable and that the sample size was large enough to detect variation of the measured parameter a
Mean percent reduction in hair pull test from baseline for placebo and Cynatine HNS. ∗∗
Mean percent change in amino acid profile from baseline for placebo and Cynatine HNS. ∗∗
Mean change in hair brightness from baseline for placebo and Cynatine HNS. ∗∗
All five measures of the nails appearance in the Cynatine HNS group are statistically significant to both baseline and placebo by Day 60 and all have a value of
There were no adverse events reported during the study, with 2 withdrawals. Both withdrawals were deemed by the principle examiner not to be related to either the active or the placebo group. Both withdrawals were because the subject claimed intolerance to the product, but this occurred after 30 days in the active group and 60 days in the placebo group. Based on this the examiner determined that it was individual susceptibility that was the cause of the intolerance. Both the active and the placebo groups were well tolerated in study with 100% of the subjects finishing the study saying they were well tolerated. Subjects in the active group also gave the product either an excellent or a good score in the products acceptability. Based on this, Cynatine HNS was found to be safe and well tolerated in this study.
A eutrophic effect for hair on the head was seen after 3 months of treatment. This was demonstrated by the decrease of hair shedding in the pull test. The Cynatine HNS group showed significantly less hair loss after 30, 60, and 90 days which were significantly different to the placebo group. This could be explained by the improvement of the anagen and telogen phases of the hair. In the Cynatine HNS group both growth phase (anagen) and stationary phase (telogen) improved resulting in less hair being pulled out. This was not seen in the placebo group. Amino acid composition of serine, glutamic acid, cystine, and methionine improved in the Cynatine HNS group significantly to give the hair a better quality. This can be explained by the addition of the various bioavailable amino acids from keratin, which is part of the Cynatine HNS formula. With an improvement in the hair quality its mechanical properties also improved significantly at Day 90 compared to placebo. Even the clinical evaluation by the physician concluded that hair shininess and brightness had improved in the Cynatine HNS group in 87.5% of the subjects compared to only 16.7% in the placebo group. An overall assessment of hair brightness showed a 64.7% change compared to only 17.6% in placebo. This is more than a 3x improvement in hair brightness at the end of the test period.
Nails also improved their condition after 1, 2, and 3 months of treatment as demonstrated by the increase of the subjects having hard and resistant nails and the decrease of the subjects having broken and roughened nails. Hardness of nails improved from 37.5% of subjects reporting hard nails to 87.5% at the end of 90 days. That goes hand in hand with the improvement in resistance and none broken nails. The placebo group scored in all categories below 17%. As the nails improved in hardness and resistance they also improved significantly in smoothness at Day 90 compared to placebo. They also changed to a more normal color than the yellow discoloration seen. The clinical evaluation by a physician also went along the same lines and an improvement in tendency to break was seen in 87.5% of subjects as compared to only 28.6% in the placebo group.
In a questionnaire administered after completion of the study, participants were asked to rate how effective they felt the products were. Not surprisingly, the placebo scored poorly in the questionnaire as 87.5% of the participants felt that it was ineffective for hair and 84.4% felt that it was poor for nails. In the Cynatine HNS group, 91.7% of the participants felt that the product was sufficient for hair with 50% feeling that the product was either very good or excellent. For nails, 87.5% of the Cynatine HNS group felt that the product was sufficient with 66.6% finding it very good or excellent.
Based on the results of this study, it would be recommended that further clinical analysis should be performed on Cynatine HNS. In order to better analyze the effect of Cynatine HNS on hair and nails a study which includes men and women, a larger sample size, and a longer duration should be performed. Additionally it would be beneficial to look at a comparison of Cynatine with and without the additional vitamins and minerals.
In conclusion, the results obtained for the Cynatine HNS group were statistically different from that obtained for the placebo group, demonstrating that Cynatine HNS had a significant influence on the quality of skin, hair, and nails. Cynatine HNS contains ingredients that are all seen as nutrients for skin, hair, and nails. Keratin is a major structural component of the hair and nails which can be seen by the influence Cynatine HNS has on the quality of hair and nails.
Robert H. Veghte is the General Manager of Roxlor Global, LLC. Neither Christina Beer nor Simon Wood is an employee of Roxlor Global, LLC, nor do they receive any royalty or payment based on performance of the product; they do however receive consulting fees on a per job basis from Roxlor Global, LLC.
The authors would like to thank Roxlor Global, LLC, for providing all the raw materials in this study. Roxlor Global, LLC, funded this study.