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The Influence of Skin Pigmentation on UVB Induced Vitamin D Increase

2018年1月29日 更新者:Pameli Datta、Bispebjerg Hospital

Vitamin D and Skin Pigmentation in Healthy Humans Exposed to UVB

Skin pigmentation (melanin) absorbs ultra violet type B (UVB) radiation found in sunlight and is believed to be responsible for darker-skinned persons' generally low 25(OH)D status. This phenomenon is found in immigrants living in Northern countries and their 25(OH)D responses to UVB-irradiation seem low.

We hypothesized that objectively measured skin pigmentation and/or pigment genes influence UVB-induced 25(OH)D increase significantly in combination with other influential parameters.

The influence of objectively measured constitutive and facultative skin pigmentation on UVB-induced 25(OH)D increase over time was investigated together with other possible influential parameters. These other influential parameters include sex, age, weight, height, BMI, number of fatty fish meals per week, Fitzpatrick Skin Type and 25(OH)D start level. The genetic parameters include 33 Vitamin D receptor and pigment SNPs.

This is a single-centre, open and non-blinded clinical trial. No randomisation was used, as the participants were allocated into two groups based on their Fitzpatrick Skin type and ethnic origin. The light-skinned group included participants with Fitzpatrick Skin type II-IV and were of Northern origin (Denmark, the Faroe Islands and the UK). The darker-skinned included Fitzpatrick Skin Types V-VI originating from countries located at latitudes below 50 degrees N. Thus, it could be ensured that the participants represented a wide range of skin pigmentation. The light-skinned (N = 22) and the darker-skinned subjects (N = 18) were exposed to identical UVB doses on identical body areas over nine weeks with weekly measurements of 25(OH)D. The UVB-induced 25(OH)D synthesis was investigated in summer-pigmented skin with melanin throughout the epidermis and during winter when ambient UVB exposure is negligible. Demographic data (gender, age, weight, height, Fitzpatrick Skin Type, measured constitutive and facultative skin pigmentation (PPF)) was collected/measured and registered in prior to study start. The number of daily consumed fatty fish meals was recorded in a questionnaire. Serum 25(OH)D was analysed weekly.

研究概览

地位

完全的

详细说明

Background. Melanin molecules (pigment) in skin, absorb UVB and presumably reduce the photo-conversion of 7-dehydrocholesterol. Epidemiological studies have reported poor vitamin D status in relatively darker-skinned immigrants residing in countries located at high latitudes. It is therefore commonly believed that skin pigmentation is a major influencer of vitamin D status. However, controlled UVB intervention studies have yielded conflicting results regarding the influence of skin pigmentation on UVB induced vitamin D increase.

Study hypothesis. The investigators hypothesized that objectively measured skin pigmentation (assessed as Pigment Protection Factor) and/or pigment genes influence UVB-induced 25-hydroxyvitamin D (25(OH)D) increase significantly in combination with other influential parameters. These other influential parameters include sex, age, weight, height, BMI, number of fatty fish meals per week, Fitzpatrick Skin Type and 25(OH)D start level. The genetic parameters include 33 Vitamin D receptor- and pigment-SNPs.

Study design. This is a single-centre, open and non-blinded clinical trial.

Intervention. The study was planned so that all included participants would receive identical UVB doses gradually increasing over nine weeks from November to January. The total UVB dose during the nine weeks was planned to be 26 kilo Joules/m2 (56 standard erythema doses). Irradiation time would be determined and regulated by measuring UV intensity with a Sola-Hazard spectroradiometer at study start, after five weeks and at the end of the exposure period. To avoid erythema, the standard erythema dose must be below the lowest measured UVB tolerance in the participants included. Based on previous experience of measurement on light-skinned individual, the UVB treatment dose was set to a maximum of 1.4 kilo Joules/m2 (3 standard erythema doses).

Methodological aspects.

Skin pigmentation. The content of melanin in epidermal biopsies is significantly correlated to measurement of pigment protection factor (PPF). This measurement of PPF can be performed non-invasively with a skin reflectance meter (UV-Optimize Scientific, Chromo-light, Denmark). In the following, PPF is therefore used as a measure of skin pigmentation and referred to as such. The measuring range of PPF is 1 to 25, meaning that a UVB dose between 1 standard erythema dose and 25 standard erythema doses is needed to elicit a just perceptible erythema. The constitutive PPF was measured on the buttocks, a body area not normally exposed to UVB. The facultative PPF was assessed as a mean of measurements on the chest, midriff, back of shoulder, and the medial and lateral sides of the arm. These are body areas influenced by prior lifelong solar exposure. Both constitutive PPF and facultative PPF were measured at study start, after 4½ weeks, and at study end. Mean values at these time-points for each parameter were used for further investigation. Furthermore, subjects self-reported their skin photo-type according to Fitzpatrick's criteria was assessed.

Blood analysis. Serum 25(OH)D was analyzed on a liquid chromatography tandem mass spectrometer (LC-MS/MS), which is the current most accurate method for this analysis. This method has been cross checked against another clinical laboratory and proven reliable.

Analytical variability. To minimize analysis variance, at least triplet analyses (technical replicates) were performed of PPF measurement and 25(OH)D analysis. All 25(OH)D samples from the same subject were analyzed in one batch. An internal standard solution with 25(OH)D was used in each run.

The total relative standard deviation (SD) varied between 4.9% at 20 nmol/l and 14.1% at 222 nmol/l reflecting experimental variability.

Biological variability. By including 10 measuring time points for serum 25(OH)D per participant, the intra-individual variability was reduced. Serum 25(OH)D is known to variate with season and solar exposure. This study was therefore conducted during winter half-year, when ambient UVB radiation and solar-exposed body areas are negligible at this time of the year (17).

Genetic parameters. SNP genotyping. A total of 33 SNPs were investigated. SNPs located in the Vitamin D Receptor (VDR) gene. The influence of the vitamin D receptor gene was investigated by genotyping the two single nucleotide polymorphisms (SNP), rs1544410 (BsmI) and rs2228570 (FokI), located in the gene (ENSG00000111424, Chromosome 12q13) as previously described. These two SNPs were selected due to their association with bone diseases as well as many other diseases, thereby indicating that polymorphisms in those regions of VDR were important for the functioning of VDR. These two SNPs were investigated together with the other investigated demographic parameters.

SNPs located in genes with influence on pigment. Thirty-one SNPs were selected according to potential influence on pigment.

All SNPs were genotyped. SNPs with genotype subgroups containing less than five subjects were merged with other allele-sharing subgroups. Heterozygote subgroups with less than five subjects was merged with an allele-sharing subgroup displaying insignificant (P > 0.05) difference in influence on the 25(OH)D increase rate. SNPs with no allele dose effect or dominant allele effect on 25(OH)D were excluded. For SNPs with dominant allele effect, subgroups with no significant differences in influence on 25(OH)D increase rate were merged according to allele sharing.

Selection of participants. Participants were included and allocated into a light-skinned group and a darker-skinned group based on Fitzpatrick Skin Type (self-reported skin photo-type) and ethnic origin. The light-skinned included Fitzpatrick Skin Types I-IV originating from Northern countries (Denmark, the Faroe Islands and the UK). The darker-skinned included Fitzpatrick Skin Types V-VI originating from countries located at latitudes below 50 degrees N. Thus, it could be ensured that the participants represented a wide range of skin pigmentation. All participants must reside in Denmark. Furthermore, an equal sex distribution was attempted.

Statistical considerations.

Randomization. No randomization was used, as the participants were allocated into two groups based on other criteria at inclusion. Both groups received identical intervention and blinding was therefore not used.

Size of study. SD was 14.1 nmol/l for high-end 25(OH)D samples. On the basis of a previous study lasting two weeks (10), the expected detectable difference was 15 nmol/l. The sample size corresponding to number of subjects required to complete the study was 16 subjects in each group, given a significance level of 5% and 80 % power to detect a difference of 15 nmol/l. Due to the relatively long study period, a minimum of 21 subjects were included in each group allowing five drop-outs. Three subjects dropped out from the darker-skinned group, and none from the light-skinned group.

Data collection. All participants were assigned with a unique study number prior to study start. Demographic data (gender, age, weight, height, Fitzpatrick Skin Type, measured constitutive and facultative skin pigmentation (PPF)) was collected/measured and registered in prior to study start. The number of daily consumed fatty fish meals was recorded in a questionnaire. All forms were marked with the participants unique study number. 25(OH)D samples were analyzed after study end. The participant study number linked to participant contact details were held in a separate sheet kept securely and in line with the regulation of the Danish Data Protection Agency.

Background diet and change in diet during intervention. The number of daily consumed fatty fish meals was recorded in a questionnaire during the study period as this parameter potentially can influence the primary outcome measure, 25(OH)D increase over time. The questionnaire was examined for errors weekly and to ensure compliance.

Background health status and lifestyle, and changes in health status and lifestyle during intervention.

The health status of the participants and start of new medication was monitored weekly throughout the study.

Adverse events. As the intervention included UVB radiation, all participants were assessed for and requested to report skin erythema.

Compliance. To optimize compliance in this long-term study, the participants were requested to schedule weekly intervention dates and complete all planned intervention throughout the study period. Furthermore, it was required that all participants had weekly blood samples and measurement of skin pigmentation three times during the study period. Also it was required that a diet questionnaire was completed and checked for errors on a weekly basis. All participants were informed thoroughly of the study requirements prior to inclusion. The acceptable level of compliance was defined at a completion of the entire intervention planned, assessment of all objective measurements and completion of all questionnaires.

Statistical analysis. Descriptive statistics of participants by group will be presented to characterize the participants included in the study. Individual data were tested with the Kolmogorov-Smirnov test to assess whether the data were normally distributed. Normally distributed data will be tested by 2-tailed t test. Otherwise non-parametric tests will be used such as 2-tailed Mann-Whitney's test or Kruskal-Wallis test. Comparison of 25(OH)D levels at different time points will be performed using paired t test (2-tailed). Categorical data will be tested with Fisher's exact test or Pearson's Chi-square test (2-tailed).

As the light-skinned group and the darker-skinned group may differ, these two groups will initially be investigated separately to examine whether there is basis to merge these two groups for common analysis. Therefore, the increase in 25(OH)D over time will be investigated separately in the light-skinned group and the darker-skinned group the following models: linear, inverse, quadratic, cubic, power, sigmoid and exponential. The derivate function was defined as the average daily change in 25(OH)D between two sample time-points (Δ25(OH)D per day). Selection of the best suitable model will be performed based on the accordance between the investigations of the 25(OH)D increase over time (individual- and group-based) and the derivate function.

The inter-individual variations in the combined group in a linear transformation of the increase of 25(OH)D over time will be explored by comparing general linear models (GLMs) with: (1) common increase rate (25(OH)D increase per day and slope) and common 25(OH)D start level (intercept), (2) common increase rates and individual intercepts (measured 25(OH)D start levels) and (3) individual increase rates (i.e. an individual constant) and measured 25(OH)D start levels.

The influence of parameters (secondary outcome measures) on the variation of the 25(OH)D increase rate will be examined separately. As the influence of separate significant parameters may not be independent, separate significant parameters will subsequently be investigated by a stepwise backward elimination of a combined GLM according to P-value (25).

Data will be statistically analyzed using SPSS 24.0 for Windows (SPSS Inc., Chicago, U.S.A.). P < 0.05 will be considered significant. No interim analysis will be performed.

研究类型

介入性

注册 (实际的)

43

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Copenhagen NV、丹麦、2400
        • Department of Dermatology, D92, Bispebjerg Hospital

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

是的

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Fitzpatrick Skin type I-IV (light-skinned)
  • Fitzpatrick Skin type V-VI (darker-skinned).

Exclusion Criteria:

  • Vitamin D supplementation exceeding 10 µg/day one month prior to study start
  • Vitamin D supplementation during study period
  • Sun holiday south of latitude 45 degrees N one month prior to or during the study start
  • Use of solarium one month prior to or during the study period
  • Chronic disease
  • Skin disease
  • Intake of cholesterol-lowering or photosensitising medication
  • Pregnancy
  • Drug addiction
  • Psychiatric disorder
  • Physical disabilities.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:基础科学
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Long-term UVB radiation
All participants received repeated UVB radiation for nine weeks. The treatment was identical for all participants.

UVB treatment regimen:

Week 1-2: 0.85 kilo Joule/m2 twice per week Week 3-7: 0.85 kilo Joule/m2 three times per week Week 8-9: 1.4 kilo Joule/m2 three times per week

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Change in serum 25(OH)D
大体时间:Measured at study start and weekly over nine weeks
Serum 25(OH)D is a marker of vitamin D increase induced by UVB
Measured at study start and weekly over nine weeks

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Hans C Wulf, Professor、Bispebjerg Hospital

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2010年11月1日

初级完成 (实际的)

2011年1月22日

研究完成 (实际的)

2011年6月25日

研究注册日期

首次提交

2018年1月10日

首先提交符合 QC 标准的

2018年1月17日

首次发布 (实际的)

2018年1月24日

研究记录更新

最后更新发布 (实际的)

2018年1月31日

上次提交的符合 QC 标准的更新

2018年1月29日

最后验证

2018年1月1日

更多信息

与本研究相关的术语

其他研究编号

  • Dpigment2010

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

IPD 计划说明

Individual participant data will be shared if it is requested at publication.

药物和器械信息、研究文件

研究美国 FDA 监管的药品

研究美国 FDA 监管的设备产品

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

UVB radiation的临床试验

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