Highlights
- •Pleiotropy and epistasis increase the complexity of human traits determination.
- •Overlapping associations for hair-related traits demonstrated for 24 literature loci.
- •Novel associations of the IGFBP5 and VDR genes with hair traits were discovered.
- •Analysed SNPs explain ∼5–30% of the variation observed in particular hair traits.
- •Hairiness in females and monobrow predicted with AUC= 0.69 and 0.68, respectively.
Abstract
Genetic prediction of different hair phenotypes can help reconstruct the physical
appearance of an individual whose biological sample is analyzed in criminal and identification
cases. Up to date, forensic prediction models for hair colour, hair shape, hair loss
and hair greying have been developed, but studies investigating predictability of
hair thickness and density traits are missing. First data suggesting overlapping associations
in various hair features have emerged in recent years, suggesting partially common
genetic basis and molecular mechanisms, and this knowledge can be used for predictive
purposes. Here we aim to broaden our understanding of the genetics underlying head,
facial and body hair thickness and density traits and examine the association for
a set of literature SNPs. We characterize the overlap in SNP association for various
hair phenotypes, the extent of genetic interactions and the potential for genetic
prediction. The study involved 999 samples from Poland, genotyped for 240 SNPs with
targeted next-generation sequencing. Logistic regression methods were applied for
association and prediction analyses while entropy-based approach was used for interaction
testing. As a result, we refined known associations for monobrow and hairiness (PAX3, 5q13.2, TBX) and identified two novel association signals in IGFBP5 and VDR. Both genes were among top significant loci, showed broad association with different
hair-related traits and were implicated in multiple interaction effects. Overall,
for 14.7% of SNPs previously associated with head hair loss and/or hair shape, a positive
signal of association was revealed with at least one hair feature studied in the current
research. Overlap in association with at least two hair-related traits was demonstrated
for 24 distinct loci. We showed that the associated SNPs explain ∼5–30% of the variation
observed in particular hair traits and allow moderate accuracy of prediction. The
highest accuracy was achieved for hairiness level prediction in females (AUC = 0.69
for the “none”, 0.69 for the “low” and 0.76 for the “excessive” hairiness category)
and monobrow (AUC = 0.69 for the “none”, 0.62 for the “slight” and 0.70 for the “significant”
monobrow category) with 33% of the variation in hairiness level in females explained
by 7 SNPs and age, and 20% of the variation in monobrow captured by 7 SNPs and sex.
Our study presents clear evidence of pleiotropy and epistasis in the genetics of hair
traits. The acquired knowledge may have practical application in forensics, as well
as in the cosmetic industry and anthropological research.
Keywords
To read this article in full you will need to make a payment
Purchase one-time access:
Academic & Personal: 24 hour online accessCorporate R&D Professionals: 24 hour online accessOne-time access price info
- For academic or personal research use, select 'Academic and Personal'
- For corporate R&D use, select 'Corporate R&D Professionals'
Subscribe:
Subscribe to Forensic Science International: GeneticsAlready a print subscriber? Claim online access
Already an online subscriber? Sign in
Register: Create an account
Institutional Access: Sign in to ScienceDirect
References
- 10 Years of GWAS discovery: biology, function, and translation.Am. J. Hum. Genet. 2017; 101: 5-22https://doi.org/10.1016/j.ajhg.2017.06.005
- An expanded view of complex traits: from polygenic to omnigenic.Cell. 2017; 169: 1177-1186https://doi.org/10.1016/j.cell.2017.05.038
- Extreme polygenicity of complex traits is explained by negative selection.Am. J. Hum. Genet. 2019; 105: 456-476https://doi.org/10.1016/j.ajhg.2019.07.003
- Evaluation of DNA variants associated with androgenetic alopecia and their potential to predict male pattern baldness.PLoS ONE. 2015; 10https://doi.org/10.1371/journal.pone.0127852
- Towards broadening Forensic DNA phenotyping beyond pigmentation: improving the prediction of head hair shape from DNA.Forensic Sci. Int.: Genet. 2018; 37: 241-251https://doi.org/10.1016/j.fsigen.2018.08.017
- Model-based prediction of human hair color using DNA variants.Hum. Genet. 2011; 129: 443-454https://doi.org/10.1007/s00439-010-0939-8
- The HIrisPlex-S system for eye, hair and skin colour prediction from DNA: Introduction and forensic developmental validation.Forensic Sci. Int.: Genet. 2018; 35: 123-135https://doi.org/10.1016/j.fsigen.2018.04.004
- Prediction of male-pattern baldness from genotypes.Eur. J. Hum. Genet. 2016; 24: 895-902https://doi.org/10.1038/ejhg.2015.220
- Exploration of SNP variants affecting hair colour prediction in Europeans.Int. J. Leg. Med. 2015; 129: 963-975https://doi.org/10.1007/s00414-015-1226-y
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data.BMC Genom. 2020; 21https://doi.org/10.1186/s12864-020-06926-y
- A scan for genetic determinants of human hair morphology: EDAR is associated with Asian hair thickness.Hum. Mol. Genet. 2008; 17: 835-843https://doi.org/10.1093/hmg/ddm355
- FGFR2 is associated with hair thickness in Asian populations.J. Hum. Genet. 2009; 54: 461-465https://doi.org/10.1038/jhg.2009.61
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations.Sci. Rep. 2018; 8https://doi.org/10.1038/s41598-018-27145-2
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features.Nat. Commun. 2016; 7https://doi.org/10.1038/ncomms10815
- Genome-wide association studies and CRISPR/Cas9-mediated gene editing identify regulatory variants influencing eyebrow thickness in humans.PLoS Genet. 2018; 14https://doi.org/10.1371/journal.pgen.1007640
- Detection and interpretation of shared genetic influences on 42 human traits.Nat. Genet. 2016; 48: 709-717https://doi.org/10.1038/ng.3570
- An atlas of genetic correlations across human diseases and traits.Nat. Genet. 2015; 47: 1236-1241https://doi.org/10.1038/ng.3406
- Abundant pleiotropy in human complex diseases and traits.Am. J. Hum. Genet. 2011; 89: 607-618https://doi.org/10.1016/j.ajhg.2011.10.004
- Toward a molecular understanding of pleiotropy.Genetics. 2006; 173: 1885-1891https://doi.org/10.1534/genetics.106.060269
- The ubiquitous nature of epistasis in determining susceptibility to common human diseases.Hum. Hered., Hum. Hered. 2003; : 73-82https://doi.org/10.1159/000073735
- Finding the epistasis needles in the genome-wide haystack.in: Epistasis: Methods and Protocols. Springer, New York2014: 19-33https://doi.org/10.1007/978-1-4939-2155-3_2
- Regionalisation of the skin.Semin. Cell Dev. Biol. 2014; 25–26: 3-10https://doi.org/10.1016/j.semcdb.2013.12.007
- Androgenetic alopecia: identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology.J. Invest. Dermatol. 2013; 133: 1489-1496https://doi.org/10.1038/jid.2013.43
- Evaluation of the predictive capacity of DNA variants associated with straight hair in Europeans.Forensic Sci. Int.: Genet. 2015; 19: 280-288https://doi.org/10.1016/j.fsigen.2015.09.004
- The adaptive variant EDARV370A is associated with straight hair in East Asians.Hum. Genet. 2013; 132: 1187-1191https://doi.org/10.1007/s00439-013-1324-1
- Genome-wide scans reveal variants at EDAR predominantly affecting hair straightness in Han Chinese and Uyghur populations.Hum. Genet. 2016; 135: 1279-1286https://doi.org/10.1007/s00439-016-1718-y
- Common variants in the trichohyalin gene are associated with straight hair in Europeans.Am. J. Hum. Genet. 2009; 85: 750-755https://doi.org/10.1016/j.ajhg.2009.10.009
- Genetic prediction of male pattern baldness.PLoS Genet. 2017; 13https://doi.org/10.1371/journal.pgen.1006594
- A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.PLoS Genet. 2008; 4https://doi.org/10.1371/journal.pgen.1000074
- The hair cycle and Vitamin D receptor.Arch. Biochem. Biophys. 2012; 523: 19-21https://doi.org/10.1016/j.abb.2011.10.002
- Effects of IGF-binding protein 5 in dysregulating the shape of human hair.J. Invest. Dermatol. 2011; 131: 320-328https://doi.org/10.1038/jid.2010.309
- The vitamin D receptor is a Wnt effector that controls hair follicle differentiation and specifies tumor type in adult epidermis.PLoS ONE. 2008; 3https://doi.org/10.1371/journal.pone.0001483
- Role of the vitamin D receptor in hair follicle biology.J. Steroid Biochem. Mol. Biol. 2007; 103: 344-346https://doi.org/10.1016/j.jsbmb.2006.12.036
- FGF signals specifically regulate the structure of hair shaft medulla via IGF-binding protein 5.Development. 2005; 132: 2981-2990https://doi.org/10.1242/dev.01873
- Identification of allelic heterogeneity at type-2 diabetes loci and impact on prediction.PLoS ONE. 2014; 9https://doi.org/10.1371/journal.pone.0113072
- Common DNA variants predict tall stature in Europeans.Hum. Genet. 2014; 133: 587-597https://doi.org/10.1007/s00439-013-1394-0
- Further evidence for population specific differences in the effect of DNA markers and gender on eye colour prediction in forensics.Int. J. Leg. Med. 2016; 130: 923-934https://doi.org/10.1007/s00414-016-1388-2
- Prediction of eye color from genetic data using bayesian approach.J. Forensic Sci. 2012; 57: 880-886https://doi.org/10.1111/j.1556-4029.2012.02077.x
- Network-based regularization for high dimensional SNP data in the case-control study of Type 2 diabetes.BMC Genet. 2017; 18https://doi.org/10.1186/s12863-017-0495-5
J. Friedman, T. Hastie, R. Tibshirani, R. Tibshirani, Regularization Paths for Generalized Linear Models via Coordinate Descent, n.d.
- A deeper look at two concepts of measuring gene–gene interactions: logistic regression and interaction information revisited.Genet. Epidemiol. 2018; 42: 187-200https://doi.org/10.1002/gepi.22108
- Testing the significance of interactions in genetic studies using interaction information and resampling technique.in: Lecture Notes in Computer Science (Including Subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). Springer, 2020: 511-524https://doi.org/10.1007/978-3-030-50420-5_38
- Finding the missing heritability of complex diseases.Nature. 2009; 461: 747-753https://doi.org/10.1038/nature08494
- Krox20, a novel candidate for the regulatory hierarchy that controls hair shaft bending.Mech. Dev. 2006; 123: 641-648https://doi.org/10.1016/j.mod.2006.06.001
- Segmental Igfbp5 expression is specifically associated with the bent structure of zigzag hairs.Mech. Dev. 2005; 122: 988-997https://doi.org/10.1016/j.mod.2005.04.012
- Vitamin D receptor signaling mechanisms: Integrated actions of a well-defined transcription factor.Steroids. 2013; 78: 127-136https://doi.org/10.1016/j.steroids.2012.10.019
- Kumaran, correlation of vitamin D and vitamin D receptor expression in patients with alopecia areata: a clinical paradigm.Int. J. Dermatol. 2018; 57: 217-222https://doi.org/10.1111/ijd.13851
- GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk.Nat. Commun. 2017; 8https://doi.org/10.1038/s41467-017-01490-8
- Variation in the RPTN gene may facilitate straight hair formation in Europeans and East Asians.J. Dermatol. Sci. 2018; 91: 331-334https://doi.org/10.1016/j.jdermsci.2018.06.003
- DNA-based predictive models for the presence of freckles, Forensic Science.Int.: Genet. 2019; 42: 252-259https://doi.org/10.1016/j.fsigen.2019.07.012
- Gene-gene interactions contribute to eye colour variation in humans.J. Hum. Genet. 2011; 56: 447-455https://doi.org/10.1038/jhg.2011.38
- Digital quantification of human eye color highlights genetic association of three new loci.PLoS Genet. 2010; 6: 34https://doi.org/10.1371/journal.pgen.1000934
- Furth. Dev. Forensic eye Color Predict. tests. 2013; https://doi.org/10.1016/j.fsigen.2012.05.009
- Trichohyalin mechanically strengthens the hair follicle: Multiple cross-bridging roles in the inner root sheath.J. Biol. Chem. 2003; 278: 41409-41419https://doi.org/10.1074/jbc.M302037200
- The biology and genetics of curly hair.Exp. Dermatol. 2017; 26: 483-490https://doi.org/10.1111/exd.13347
- Hair coloration by gene regulation: fact or fiction?.Trends Biotechnol. 2015; 33: 707-711https://doi.org/10.1016/j.tibtech.2015.10.001
- Human disease variation in the light of population genomics.Cell. 2019; 177: 115-131https://doi.org/10.1016/j.cell.2019.01.052
- Complex-trait prediction in the era of big data.Trends Genet. 2018; 34: 746-754https://doi.org/10.1016/j.tig.2018.07.004
- Will big data close the missing heritability gap?.Genetics. 2017; 207: 1135-1145https://doi.org/10.1534/genetics.117.300271
- Receiver operating characteristic curve in diagnostic test assessment.J. Thorac. Oncol. 2010; 5: 1315-1316https://doi.org/10.1097/JTO.0b013e3181ec173d
- Principles and practical application of the receiver-operating characteristic analysis for diagnostic tests.Prev. Vet. Med. 2000; 45: 23-41https://doi.org/10.1016/S0167-5877(00)00115-X
- Phenotypes and Genotypes.Springer, London, London2016https://doi.org/10.1007/978-1-4471-5310-8
- Simultaneous analysis of all SNPs in genome-wide and re-sequencing association studies.PLoS Genet. 2008; 4https://doi.org/10.1371/journal.pgen.1000130
- Network-constrained regularization and variable selection for analysis of genomic data.Bioinformatics. 2008; 24: 1175-1182https://doi.org/10.1093/bioinformatics/btn081
- The sparse laplacian shrinkage estimator for high-dimensional regression.Ann. Stat. 2011; 39: 2021-2046https://doi.org/10.1214/11-AOS897
- Integrative analysis of gene-environment interactions under a multi-response partially linear varying coefficient model.Stat. Med. 2014; 33: 4988-4998https://doi.org/10.1002/sim.6287
- MRMRe: An R package for parallelized mRMR ensemble feature selection.Bioinformatics. 2013; 29: 2365-2368https://doi.org/10.1093/bioinformatics/btt383
- Gene–Environment Interaction: A Variable Selection Perspective.in: Methods in Molecular Biology. Humana Press Inc., 2021: 191-223https://doi.org/10.1007/978-1-0716-0947-7_13
- Meta-analysis of genome-wide association studies identifies 8 novel loci involved in shape variation of human head hair.Hum. Mol. Genet. 2018; 27: 559-575https://doi.org/10.1093/hmg/ddx416
- Web-based, participant-driven studies yield novel genetic associations for common traits.PLoS Genet. 2010; 6: 1-20https://doi.org/10.1371/journal.pgen.1000993
- Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness.Nat. Commun. 2017; 8https://doi.org/10.1038/ncomms14694
- Six novel susceptibility loci for early-onset androgenetic alopecia and their unexpected association with common diseases.PLoS Genet. 2012; 8https://doi.org/10.1371/journal.pgen.1002746
- Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldness.Br. J. Dermatol. 2011; 165: 1293-1302https://doi.org/10.1111/j.1365-2133.2011.10708.x
- EDA2R is associated with androgenetic alopecia.J. Invest. Dermatol. 2008; 128: 2268-2270https://doi.org/10.1038/jid.2008.60
- Fine mapping of the human AR/EDA2R locus in androgenetic alopecia.Br. J. Dermatol. 2010; 162: 899-903https://doi.org/10.1111/j.1365-2133.2010.09649.x
Article info
Publication history
Published online: March 25, 2022
Accepted:
March 22,
2022
Received in revised form:
February 25,
2022
Received:
December 8,
2021
Identification
Copyright
© 2022 Elsevier B.V. All rights reserved.