Evidence map›Paper›PMID 42510836›Full record

ArticleGenes2026

Mitochondrial DNA Variation in Human Hair Shafts Influenced by Physical Characteristics: A Massively Parallel Sequencing Analysis.

Nana Wang, Jiajun Liu, Dan Peng, Jiaojiao Geng, Enlin Wu, Hui Liang, Riga Wu, Ran Li, Hongyu Sun

Abstract read
In one paragraph

Article in Genes, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Nana WangSchool of Nursing, Guiyang Kangyang University, Guiyang 550081, China.
Jiajun LiuFaculty of Forensic Medicine, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China.
Dan PengFaculty of Forensic Medicine, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China.
Jiaojiao GengFaculty of Forensic Medicine, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China.
Enlin WuFaculty of Forensic Medicine, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China.ORCID 0009-0006-9113-4136
Hui LiangSchool of Nursing, Guiyang Kangyang University, Guiyang 550081, China.
Riga WuFaculty of Forensic Medicine, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China.ORCID 0000-0002-8594-2843
Ran LiFaculty of Forensic Medicine, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China.ORCID 0000-0001-6473-4570
Hongyu SunFaculty of Forensic Medicine, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China.

Funding

the High-level Talent Research Start-up Fund of Guiyang Kangyang University No. K2026-010the National Key R&D Program of China No.2024YFC3306702the Natural Science Foundation of Guangdong Province No.2023A1515030223the Science and Technology Program of Guangzhou No.202201011379
6 · The paper itself

Abstract

BACKGROUND/

objectivesHair shafts are frequently encountered as forensic evidence, but their limited nuclear DNA content often constrains short tandem repeat (STR) profiling. Mitochondrial DNA (mtDNA) analysis provides an alternative approach; however, the extent to which hair-shaft physical characteristics affect MPS-derived mtDNA read counts, degradation state, and point heteroplasmy (PHP) remains insufficiently characterized. This study aimed to evaluate these associations in human hair shaft samples.

methodsmtDNA hypervariable regions were analyzed in 907 hair shaft fragments from 183 donors using the MGIEasy Signature Identification Library Prep Kit and massively parallel sequencing. Samples were grouped by hair-shaft length, longitudinal segment, scalp region, color, diameter, donor sex, and cosmetic treatment. MPS read counts were used as semi-quantitative indicators of relative mtDNA representation, the HVR7/HVR5 read-count ratio was used as an indirect indicator of degradation state, and PHP was called at a minor allele frequency of ≥10% with a sequencing depth of ≥100× at the site.

resultsUnder the present workflow, hair shafts generated higher mtDNA read counts than paired bloodstains, and PHP was detected more frequently in hair shafts than in bloodstains (15.93% versus 8.85%). In the exploratory subgroup analyses, longer hair shafts tended to show higher total MPS-derived mtDNA read counts, whereas longitudinally segmented hairs showed a tendency toward decreasing read counts and increasing degradation from the proximal to distal end. In a small paired black/white hair dataset, black hairs showed higher read counts than paired white hairs, but this observation should be interpreted cautiously. Scalp region, diameter, donor sex, and cosmetic treatment showed no consistent effects on read counts or degradation state, although cosmetic treatment was associated with descriptive differences in PHP type and regional distribution.

conclusionsThese findings suggest that selected physical characteristics of hair shafts may be associated with MPS-derived mtDNA metrics under the present workflow. However, because several subgroup analyses were based on limited sample sizes and clustered samples, these results should be regarded as exploratory and require validation in larger independent datasets.

Indexed as

DNA, MitochondrialHairHigh-Throughput Nucleotide SequencingAdultFemaleGene FrequencyGenetic VariationHeteroplasmyHumansMaleSequence Analysis, DNADNA, Mitochondrialhair shaftmassively parallel sequencing (MPS)mitochondrial DNA (mtDNA)point heteroplasmy (PHP)

Identifiers

PMID42510836
PMCPMC13409926

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.