{"title":"牛头畸形的流行:现代人类和进化观点的荟萃分析。","authors":"Pierre-Hadrien Decaup, Christine Couture, Mathieu Colin, Elsa Garot","doi":"10.1127/homo/2021/1447","DOIUrl":null,"url":null,"abstract":"<p><p>Taurodontism is a continuous anatomical variation of permanent and primary posterior teeth represented by an enlargement of the pulp cavity. A high prevalence of the trait is reported in <i>Homo neanderthalensis</i> remains. Exploring and refining epidemiology of taurodontism in actual populations could strengthen the hypothesis of a selective advantage for a high attrition diet (as heavy tooth wear in <i>Homo sapiens</i> evolution changed little until recently) or favour pleiotropic or genetic drift effects to explain the high frequency of the trait in Neandertal remains. Prevalence ranges between 0.1% and 48% in the literature. The aim of the present study is to assess the prevalence of taurodontism in recent populations by means of meta-analysis, that is, is the prevalence of taurodontism lower or higher in modern human living populations, where the selective advantages of high attrition diet are still expected? From 90 potentially eligible studies, 15 were included in the meta-analysis. Only cross-sectional studies were reported, and 14,771 participants were included. The meta-analyses were performed with a random model, calculating a weighted-mean prevalence of 11.8%. Gender was found to be unrelated to the prevalence of taurodontism (OR = 0.84 (95% CI 0.67-1.05), <i>p</i> > 0.05). Taurodontism occurs in approximately 11.8% of the living population. This result questions the status of taurodontism as a \"typical trait\" in <i>Homo neanderthalensis</i> and allows a possible common evolutionary mechanism in <i>Homo sapiens</i> and <i>Homo neanderthalensis</i> for the trait. Further studies should include more accurate and standardized methods to assess the condition.</p>","PeriodicalId":46714,"journal":{"name":"Homo-Journal of Comparative Human Biology","volume":"73 1","pages":"1-11"},"PeriodicalIF":0.7000,"publicationDate":"2022-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":"{\"title\":\"Prevalence of taurodontism: meta-analysis in recent humans and evolutionary perspectives.\",\"authors\":\"Pierre-Hadrien Decaup, Christine Couture, Mathieu Colin, Elsa Garot\",\"doi\":\"10.1127/homo/2021/1447\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Taurodontism is a continuous anatomical variation of permanent and primary posterior teeth represented by an enlargement of the pulp cavity. A high prevalence of the trait is reported in <i>Homo neanderthalensis</i> remains. Exploring and refining epidemiology of taurodontism in actual populations could strengthen the hypothesis of a selective advantage for a high attrition diet (as heavy tooth wear in <i>Homo sapiens</i> evolution changed little until recently) or favour pleiotropic or genetic drift effects to explain the high frequency of the trait in Neandertal remains. Prevalence ranges between 0.1% and 48% in the literature. The aim of the present study is to assess the prevalence of taurodontism in recent populations by means of meta-analysis, that is, is the prevalence of taurodontism lower or higher in modern human living populations, where the selective advantages of high attrition diet are still expected? From 90 potentially eligible studies, 15 were included in the meta-analysis. Only cross-sectional studies were reported, and 14,771 participants were included. The meta-analyses were performed with a random model, calculating a weighted-mean prevalence of 11.8%. Gender was found to be unrelated to the prevalence of taurodontism (OR = 0.84 (95% CI 0.67-1.05), <i>p</i> > 0.05). Taurodontism occurs in approximately 11.8% of the living population. This result questions the status of taurodontism as a \\\"typical trait\\\" in <i>Homo neanderthalensis</i> and allows a possible common evolutionary mechanism in <i>Homo sapiens</i> and <i>Homo neanderthalensis</i> for the trait. 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引用次数: 3
摘要
牛牙畸形是恒牙和乳牙的连续解剖变异,表现为牙髓腔扩大。据报道,这种特征在尼安德特人遗骸中非常普遍。在实际人群中探索和完善牛齿症的流行病学,可以加强高消耗饮食的选择优势假设(因为智人进化过程中牙齿的严重磨损直到最近才发生变化),或者支持多益性或遗传漂变效应来解释尼安德特人遗骸中这种特征的高频率。在文献中,患病率在0.1%到48%之间。本研究的目的是通过荟萃分析来评估最近人群中牛齿症的患病率,也就是说,在现代人类生活人群中,牛齿症的患病率是低还是高,高营养饮食的选择优势仍然是预期的?从90项可能符合条件的研究中,有15项纳入了meta分析。仅报道了横断面研究,包括14,771名参与者。采用随机模型进行meta分析,计算加权平均患病率为11.8%。性别与牛牙症患病率无关(OR = 0.84 (95% CI 0.67 ~ 1.05), p > 0.05)。大约11.8%的人有牛牙症。这一结果质疑了牛头畸形作为尼安德特人“典型特征”的地位,并允许智人和尼安德特人的这种特征可能存在共同的进化机制。进一步的研究应该包括更准确和标准化的方法来评估病情。
Prevalence of taurodontism: meta-analysis in recent humans and evolutionary perspectives.
Taurodontism is a continuous anatomical variation of permanent and primary posterior teeth represented by an enlargement of the pulp cavity. A high prevalence of the trait is reported in Homo neanderthalensis remains. Exploring and refining epidemiology of taurodontism in actual populations could strengthen the hypothesis of a selective advantage for a high attrition diet (as heavy tooth wear in Homo sapiens evolution changed little until recently) or favour pleiotropic or genetic drift effects to explain the high frequency of the trait in Neandertal remains. Prevalence ranges between 0.1% and 48% in the literature. The aim of the present study is to assess the prevalence of taurodontism in recent populations by means of meta-analysis, that is, is the prevalence of taurodontism lower or higher in modern human living populations, where the selective advantages of high attrition diet are still expected? From 90 potentially eligible studies, 15 were included in the meta-analysis. Only cross-sectional studies were reported, and 14,771 participants were included. The meta-analyses were performed with a random model, calculating a weighted-mean prevalence of 11.8%. Gender was found to be unrelated to the prevalence of taurodontism (OR = 0.84 (95% CI 0.67-1.05), p > 0.05). Taurodontism occurs in approximately 11.8% of the living population. This result questions the status of taurodontism as a "typical trait" in Homo neanderthalensis and allows a possible common evolutionary mechanism in Homo sapiens and Homo neanderthalensis for the trait. Further studies should include more accurate and standardized methods to assess the condition.