Unilever Research & Development, Quarry Road East, Port Sunlight, United Kingdom.
Unilever Research & Development, Quarry Road East, Port Sunlight, United Kingdom.
J Dermatol Sci. 2014 Jan;73(1):23-30. doi: 10.1016/j.jdermsci.2013.08.016. Epub 2013 Sep 10.
A single nucleotide polymorphism (SNP), 538G→A, leading to a G180R substitution in the ABCC11 gene results in reduced concentrations of apocrine derived axillary odour precursors.
Determine the axillary odour levels in the SNP ABCC11 genotype variants and to investigate if other parameters associated with odour production are affected.
Axillary odour was assessed by subjective quantification and gas chromatography headspace analysis. Metabolite profiles, microbiome diversity and personal hygiene habits were also assessed.
Axillary odour in the A/A homozygotes was significantly lower compared to the G/A and G/G genotypes. However, the perception-based measures still detected appreciable levels of axillary odour in the A/A subjects. Metabolomic analysis highlighted significant differences in axillary skin metabolites between A/A subjects compared to those carrying the G allele. These differences resulted in A/A subjects lacking specific volatile odourants in the axillary headspace, but all genotypes produced odoriferous short chain fatty acids. Microbiomic analysis revealed differences in the relative abundance of key bacterial genera associated with odour generation between the different genotypes. Deodorant usage indicated a high level of self awareness of axillary odour levels with A/A individuals less likely to adopt personal hygiene habits designed to eradicate/mask its presence.
The SNP in the ABCC11 gene results in lower levels of axillary odour in the A/A homozygotes compared to those carrying the G allele, but A/A subjects still produce noticeable amounts of axillary odour. Differences in axillary skin metabolites, bacterial genera and personal hygiene behaviours also appear to be influenced by this SNP.
ABCC11 基因中的单核苷酸多态性(SNP)538G→A 导致 G180R 取代,导致大汗腺衍生的腋窝气味前体浓度降低。
确定 SNP ABCC11 基因型变异体的腋窝气味水平,并研究是否有其他与气味产生相关的参数受到影响。
通过主观定量和气相色谱顶空分析评估腋窝气味。还评估了代谢物谱、微生物组多样性和个人卫生习惯。
A/A 纯合子的腋窝气味明显低于 G/A 和 G/G 基因型。然而,基于感知的测量方法仍然在 A/A 受试者中检测到可察觉的腋窝气味水平。代谢组学分析突出了 A/A 受试者与携带 G 等位基因的受试者之间腋窝皮肤代谢物的显著差异。这些差异导致 A/A 受试者缺乏腋窝顶空特定的挥发性气味物质,但所有基因型都产生了有气味的短链脂肪酸。微生物组分析揭示了不同基因型之间与气味产生相关的关键细菌属的相对丰度存在差异。除臭剂的使用表明 A/A 个体对腋窝气味水平有很高的自我意识,不太可能采用旨在消除/掩盖其存在的个人卫生习惯。
ABCC11 基因中的 SNP 导致 A/A 纯合子的腋窝气味水平低于携带 G 等位基因的个体,但 A/A 受试者仍会产生明显的腋窝气味。腋窝皮肤代谢物、细菌属和个人卫生行为的差异似乎也受到该 SNP 的影响。