Guardiola-Ripoll Maria, Sotero-Moreno Alejandro, Chaumette Boris, Kebir Oussama, Hostalet Noemí, Almodóvar-Payá Carmen, Moreira Mónica, Giralt-López Maria, Krebs Marie-Odile, Fatjó-Vilas Mar
FIDMAG Germanes Hospitalàries Research Foundation, 08830 Sant Boi de Llobregat, Spain.
CIBERER (Biomedical Research Network in Rare Diseases), Instituto de Salud Carlos III, 28029 Madrid, Spain.
Biomedicines. 2024 Oct 7;12(10):2270. doi: 10.3390/biomedicines12102270.
Dermatoglyphic pattern deviances have been associated with schizophrenia-spectrum disorders (SSD) and are considered neurodevelopment vulnerability markers based on the shared ectodermal origin of the epidermis and the central nervous system. The endocannabinoid system participates in epidermal differentiation, is sensitive to prenatal insults and is associated with SSD. We aimed to investigate whether the Cannabinoid Receptor 1 gene () modulates the dermatoglyphics-SSD association. In a sample of 112 controls and 97 patients with SSD, three dermatoglyphic markers were assessed: the total palmar a-b ridge count (TABRC), the a-b ridge count fluctuating asymmetry (ABRC-FA), and the pattern intensity index (PII). Two polymorphisms were genotyped: rs2023239-T/C and rs806379-A/T. We tested: (i) the association with SSD and dermatoglyphic variability within groups; and (ii) the × dermatoglyphic measures interaction on SSD susceptibility. Both polymorphisms were associated with SSD. The polymorphism rs2023239 modulated the relationship between PII and SSD: a high PII score was associated with a lower SSD risk within C-allele carriers and a higher SSD risk within TT-homozygotes. This result indicates an inverse relationship between the PII and the SSD predicted probability conditional to the rs2023239 genotype. These novel findings suggest the endocannabinoid system's role in the development and variability of dermatoglyphic patterns. The identified interaction encourages combining genetic and dermatoglyphics to assess neurodevelopmental alterations predisposing to SSD in future studies.
皮纹模式异常与精神分裂症谱系障碍(SSD)有关,基于表皮和中枢神经系统共同的外胚层起源,被认为是神经发育易损性标志物。内源性大麻素系统参与表皮分化,对产前损伤敏感且与SSD相关。我们旨在研究大麻素受体1基因()是否调节皮纹与SSD的关联。在112名对照者和97名SSD患者的样本中,评估了三种皮纹标志物:手掌a-b嵴总数(TABRC)、a-b嵴数波动不对称性(ABRC-FA)和模式强度指数(PII)。对两个多态性进行基因分型:rs2023239-T/C和rs806379-A/T。我们测试了:(i)该基因与SSD以及组内皮纹变异性的关联;(ii)该基因×皮纹测量指标对SSD易感性的相互作用。两个多态性均与SSD相关。rs2023239多态性调节了PII与SSD之间的关系:在C等位基因携带者中,高PII评分与较低的SSD风险相关,而在TT纯合子中则与较高的SSD风险相关。这一结果表明,在rs2023239基因型条件下,PII与SSD预测概率之间呈负相关。这些新发现表明内源性大麻素系统在皮纹模式的发育和变异性中的作用。所确定的相互作用促使在未来研究中结合遗传学和皮纹学来评估易患SSD的神经发育改变。