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Mind the gap: Reproducibility of methods for studying paraspinal muscles 注意间隙:研究棘旁肌肉方法的可重复性
Q3 Medicine Pub Date : 2025-08-21 DOI: 10.1016/j.tria.2025.100431
Nayia Aza , David James Halliday , Chandrasekaran Kaliaperumal

Background

We respond to a recent study on Magnetic Resonance Imaging-based measurement of paraspinal muscles in patients with chronic back pain.

Methods

We reviewed their methodology with a focus on segmentation tools and observer reliability.

Results

Key details, including the software used and inter-observer reliability, were not reported.

Conclusions

Clarifying the methodology would improve reproducibility and support comparability across studies.
我们对最近一项基于磁共振成像测量慢性背痛患者棘旁肌肉的研究做出回应。方法我们回顾了他们的方法,重点是分割工具和观察者可靠性。结果关键细节,包括使用的软件和观察者之间的信度,没有报告。结论澄清方法学将提高研究的可重复性和可比性。
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引用次数: 0
Anatomical and clinical perspectives on the distal humeral fossae: A study in South Indian dry bones 肱骨远端窝的解剖学和临床观点:南印度干骨的研究
Q3 Medicine Pub Date : 2025-08-08 DOI: 10.1016/j.tria.2025.100429
Nandini Prashanth Bhat , Ashwija Shetty , Kurian Alapatt , Nom Kumar Naik Bhukya , Sushma Prabhath , Suhani Sumalatha

Background

The distal end of the humerus features three fossae—radial, coronoid, and olecranon—that accommodate the processes of the forearm bones during elbow movements. Variations in their morphology and morphometry can influence joint biomechanics, fracture fixation, and prosthesis design. However, comprehensive data on all three fossae in South Indian dry humeri remain limited. This study aims to fill this gap by providing clinically relevant morphometric insights.

Methodology

A total of 120 adult dry humeri (60 right, 60 left) of unknown age and sex were analyzed. Standardized photographs were evaluated using ImageJ software. Sixteen parameters—including the length, width, and circumference of each fossa—were measured. Data were analyzed using descriptive statistics, Pearson's correlation, and t-tests.

Results

The left humerus was significantly longer (mean difference 1.96 cm) and had a greater distal width (mean difference 0.58 cm) than the right. The coronoid fossa was longer (mean difference 0.13 cm) and had a greater circumference on the right (mean difference 0.23 cm), while the radial and olecranon fossae were larger on left. Morphological analysis identified five olecranon fossa types, with oval being most common (44 %). The coronoid and radial fossae were predominantly triangular. No significant correlation was observed between humeral length or width and fossa circumference. The supratrochlear foramen, an anatomical variation which was found in 28.3 % of bones.

Conclusion

These findings have important implications for orthopedic surgery, such as intramedullary fixations, prosthetic design for elbow reconstruction, and forensic anthropology.
背景:肱骨远端有三个窝——桡骨窝、冠骨窝和鹰嘴窝,它们在肘部运动时容纳前臂骨突。它们形态和形态的变化会影响关节生物力学、骨折固定和假体设计。然而,关于南印度干肱骨所有三个窝的综合数据仍然有限。本研究旨在通过提供临床相关的形态学见解来填补这一空白。方法对120例年龄、性别不详的成人干肱骨(左、右各60例)进行分析。使用ImageJ软件对标准化照片进行评估。测量了16个参数,包括每个窝的长度、宽度和周长。数据分析采用描述性统计、Pearson相关和t检验。结果左肱骨明显长于右肱骨(平均差1.96 cm),远端宽度明显大于右肱骨(平均差0.58 cm)。冠状窝较长(平均差0.13 cm),右侧周长较大(平均差0.23 cm),左侧桡骨窝和鹰嘴窝较大。形态学分析鉴定出5种鹰嘴窝类型,椭圆形最为常见(44%)。冠状窝和桡骨窝主要呈三角形。肱骨长度或宽度与窝围无显著相关性。滑车上孔,在28.3%的骨骼中发现解剖变异。结论这些发现对骨科手术,如髓内固定、肘关节重建假体设计和法医人类学具有重要意义。
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引用次数: 0
A dissection and angiographic study of morphological variations in the anterior communicating artery complex in a South African sample 解剖和血管造影研究的形态变化的前交通动脉复合体在南非的样本
Q3 Medicine Pub Date : 2025-08-05 DOI: 10.1016/j.tria.2025.100426
Mbalentle Madolo , Geney Gunston , Stuart More , Kentse Mpolokeng

Background

The anterior communicating artery complex (ACAC), which includes the A1 and A2 segments of the anterior cerebral artery (ACA) and the anterior communicating artery (ACoA), is a common site for anatomical variation and aneurysm formation. While cerebral arterial variations have been linked to aneurysm development, limited data exists on these variations in the South African population.

Methods

This study assessed ACAC morphology through two components: dissection of 68 formalin-fixed adult brains (35 female, 33 male) and analysis of 200 adult magnetic resonance angiogram (MRA) scans (145 female, 55 male). Anatomical variations in the ACAC were recorded and evaluated for their prevalence and potential association with cerebral aneurysms.

Results

Variations in the ACAC were prevalent in 67.6 % of dissection specimens and 43.5 % of angiographic images. The most frequent variations of the ACoA observed in both dissection and angiographic samples were X-shaped formations and hypoplasia. In dissections, the A1 segment frequently displayed hypoplasia, duplication, and fenestration, while the A2 segment typically presented the 'anastomosed' variation. In angiographic scans, the A2 segment often exhibited a triple ACA configuration. A history of ACAC aneurysms was present in 23.9 % of MRA scans. However, no significant correlation was observed between ACAC variations and aneurysm presence.

Conclusion

This study demonstrates significant morphological diversity within the ACAC, including newly described variations, and highlights inconsistencies with existing literature regarding aneurysm association. These findings underscore the need for region-specific anatomical data to inform surgical planning and risk assessment in cerebrovascular interventions.
前交通动脉复合体(ACAC)包括大脑前动脉(ACA)和前交通动脉(ACoA)的A1和A2段,是解剖变异和动脉瘤形成的常见部位。虽然脑动脉变异与动脉瘤的发展有关,但在南非人群中关于这些变异的数据有限。方法通过解剖68例经福尔马林固定的成人大脑(女性35例,男性33例)和分析200例成人磁共振血管造影(MRA)扫描(女性145例,男性55例),对ACAC形态学进行了评估。记录ACAC的解剖变异,并评估其患病率及其与脑动脉瘤的潜在关联。结果67.6%的解剖标本和43.5%的血管造影图像存在ACAC变异。在解剖和血管造影样本中观察到的ACoA最常见的变化是x形形成和发育不全。在解剖中,A1节段经常表现为发育不全、重复和开窗,而A2节段通常表现为“吻合”变异。在血管造影扫描中,A2段通常表现为三ACA结构。23.9%的MRA扫描有ACAC动脉瘤病史。然而,ACAC变异与动脉瘤存在之间没有明显的相关性。本研究显示了ACAC内显著的形态多样性,包括新描述的变异,并强调了与现有文献关于动脉瘤关联的不一致。这些发现强调了在脑血管干预中需要特定区域的解剖数据来指导手术计划和风险评估。
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引用次数: 0
Aberrant placental structure is corrected with repeated nanoparticle-mediated IGF1 treatments in a Guinea pig model of fetal growth restriction 在胎儿生长受限的豚鼠模型中,通过重复纳米颗粒介导的IGF1治疗来纠正异常胎盘结构
Q3 Medicine Pub Date : 2025-07-19 DOI: 10.1016/j.tria.2025.100424
Baylea N. Davenport , Rebecca L. Wilson , Alyssa A. Williams , Jaimi A. Gray , Edward L. Stanley , Helen N. Jones

Background

Fetal growth restriction (FGR) is most commonly due to placental insufficiency. There are currently no treatments for placental insufficiency or FGR, and the only intervention is iatrogenic pre-term delivery. We have previously shown efficacy of repeated placental nanoparticle-mediated insulin-like 1 growth factor (IGF1) treatment in improving placental efficiency (increased fetal-placental weight ratio) and correcting fetal growth in a maternal nutrient restriction (MNR) guinea pig model of FGR. We hypothesize placenta structural changes (reduced exchange area, altered vascular structure) that we and others have previously shown in the FGR/MNR placenta which lead to deficits in placental function are mitigated by our repeated nanoparticle-mediated hIGF1 treatment.

Methods

Here we investigate the structural remodeling of the placenta in a maternal nutrient restriction (MNR) guinea pig model following 3 repeated intraplacental injections of nanoparticle-mediated hIGF1 that may underpin the published improvements in placental efficiency and fetal growth. Using immunohistochemistry and Dice-CT we investigated the micro- and macrovasculature changes of the placenta structure to identify changes in FGR and treatment.

Results

Sham-treated MNR placentas displayed disorganized microvasculature labyrinthine exchange areas with a reduction in placental capillary number and an increase in the volume of the placenta macrovasculature. Repeated nanoparticle-mediated hIGF1 treatment, however, resulted in an improved exchange area with normalized placental capillary number and macrovasculature volume.

Conclusions

This data demonstrates repeated nanoparticle-mediated hIGF1 delivery corrects aberrant placenta structure during FGR and placental insufficiency likely leading to improved gas exchange and transfer of nutrients to the fetus restoring fetal growth.
胎儿生长受限(FGR)最常见的原因是胎盘功能不全。目前尚无治疗胎盘功能不全或FGR的方法,唯一的干预措施是医源性早产。我们之前已经在母体营养限制(MNR) FGR豚鼠模型中证明了重复胎盘纳米颗粒介导的胰岛素样1生长因子(IGF1)治疗在提高胎盘效率(增加胎胎盘重量比)和纠正胎儿生长方面的有效性。我们假设,我们和其他人之前在FGR/MNR胎盘中发现的胎盘结构变化(交换面积减少,血管结构改变)导致胎盘功能缺陷,通过我们重复的纳米粒子介导的hIGF1治疗可以减轻胎盘功能缺陷。方法在母体营养限制(MNR)豚鼠模型中,我们研究了3次重复胎盘内注射纳米颗粒介导的hIGF1后胎盘的结构重塑,这可能是已发表的胎盘效率和胎儿生长改善的基础。我们利用免疫组织化学和ct检查了胎盘结构的微血管和大血管变化,以确定FGR和治疗的变化。结果经sham处理的MNR胎盘微血管迷路交换区紊乱,胎盘毛细血管数量减少,胎盘大血管体积增加。然而,重复的纳米颗粒介导的hIGF1处理导致交换面积的改善,胎盘毛细血管数量和大血管体积正常化。结论:重复的纳米颗粒介导的hIGF1传递纠正了FGR期间胎盘结构的异常,胎盘功能不全可能导致胎儿气体交换和营养物质转移的改善,从而恢复胎儿的生长。
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引用次数: 0
Early white matter microstructural alterations in cerebral small vessel disease: A tract-specific diffusion tensor imaging and cardio-cerebrovascular risk perspective 脑小血管疾病早期白质微结构改变:导管特异性弥散张量成像和心脑血管风险视角
Q3 Medicine Pub Date : 2025-07-19 DOI: 10.1016/j.tria.2025.100425
Zaw Myo Hein , Muhammad Danial Che Ramli , Usman Jaffer , Che Mohd Nasril Che Mohd Nassir

Background

Silent cerebral small vessel disease (CSVD), marked by white matter hyperintensities (WMHs), are commonly detected incidentally on neuroimaging. Emerging evidence links early brain microstructural changes to modifiable cardio-cerebrovascular risks, even without neurological symptoms. This study aimed to explore the relationship between cardio-cerebrovascular risk, white matter tract integrity, and cognitive performance in asymptomatic adults, using QRISK3 profiling, diffusion tensor imaging (DTI), and neurocognitive evaluation.

Methods

Sixty neurologically asymptomatic adults (mean age: 39.8 ± 11.5 years) with low to moderate QRISK3 scores underwent standardized neurocognitive assessment 3T brain MRI, including DTI sequences. Lesion-guided region-of-interest (ROI) tractography was used to assess six bilateral white matter tracts commonly affected in CSVD: the anterior and superior corona radiata and the superior longitudinal fasciculus (SLF).

Results

WMHs were identified in 20 individuals (33.3 %). Their presence was significantly associated with aging, systolic blood pressure, hypertension, and QRISK3 score (p < 0.05). While no significant cognitive impairment was observed, processing speed was negatively correlated with age and QRISK3. Although DTI metrics such as fractional anisotropy (FA) and mean diffusivity (MD) did not significantly differ across groups, tract-specific analysis revealed that higher QRISK3 scores were significantly associated with reduced white matter integrity in the left SLF.

Conclusion

These findings highlight the presence of early, subclinical white matter alterations in individuals at cardio-cerebrovascular risk, even in the absence of neurological symptoms. The integration of tract-specific DTI analysis with vascular risk profiling may provide a sensitive approach for detecting preclinical CSVD and guiding early intervention strategies in at-risk populations.
背景:以白质高信号(WMHs)为标志的无症状性脑血管疾病(CSVD)通常在神经影像学上偶然发现。新出现的证据将早期大脑微观结构的改变与可改变的心脑血管风险联系起来,即使没有神经系统症状。本研究旨在探讨无症状成人心脑血管风险、白质束完整性和认知表现之间的关系,采用QRISK3谱分析、弥散张量成像(DTI)和神经认知评估。方法对60名QRISK3评分中低的无神经症状成人(平均年龄:39.8±11.5岁)进行了标准化的神经认知评估3T脑MRI,包括DTI序列。病变引导感兴趣区(ROI)束道造影用于评估CSVD常见的6个双侧白质束:前、上辐射冠和上纵束(SLF)。结果20例(33.3%)患者中检出swmh。它们的存在与年龄、收缩压、高血压和QRISK3评分显著相关(p <;0.05)。处理速度与年龄和QRISK3负相关,但未观察到明显的认知障碍。尽管DTI指标(如分数各向异性(FA)和平均扩散率(MD))在各组之间没有显著差异,但通道特异性分析显示,较高的QRISK3评分与左侧SLF白质完整性降低显著相关。结论:这些发现表明,即使在没有神经系统症状的情况下,具有心脑血管风险的个体也存在早期的亚临床白质改变。将血管特异性DTI分析与血管风险分析相结合,可能为检测临床前CSVD提供一种敏感的方法,并指导高危人群的早期干预策略。
{"title":"Early white matter microstructural alterations in cerebral small vessel disease: A tract-specific diffusion tensor imaging and cardio-cerebrovascular risk perspective","authors":"Zaw Myo Hein ,&nbsp;Muhammad Danial Che Ramli ,&nbsp;Usman Jaffer ,&nbsp;Che Mohd Nasril Che Mohd Nassir","doi":"10.1016/j.tria.2025.100425","DOIUrl":"10.1016/j.tria.2025.100425","url":null,"abstract":"<div><h3>Background</h3><div>Silent cerebral small vessel disease (CSVD), marked by white matter hyperintensities (WMHs), are commonly detected incidentally on neuroimaging. Emerging evidence links early brain microstructural changes to modifiable cardio-cerebrovascular risks, even without neurological symptoms. This study aimed to explore the relationship between cardio-cerebrovascular risk, white matter tract integrity, and cognitive performance in asymptomatic adults, using QRISK3 profiling, diffusion tensor imaging (DTI), and neurocognitive evaluation.</div></div><div><h3>Methods</h3><div>Sixty neurologically asymptomatic adults (mean age: 39.8 ± 11.5 years) with low to moderate QRISK3 scores underwent standardized neurocognitive assessment 3T brain MRI, including DTI sequences. Lesion-guided region-of-interest (ROI) tractography was used to assess six bilateral white matter tracts commonly affected in CSVD: the anterior and superior corona radiata and the superior longitudinal fasciculus (SLF).</div></div><div><h3>Results</h3><div>WMHs were identified in 20 individuals (33.3 %). Their presence was significantly associated with aging, systolic blood pressure, hypertension, and QRISK3 score (<em>p</em> &lt; 0.05). While no significant cognitive impairment was observed, processing speed was negatively correlated with age and QRISK3. Although DTI metrics such as fractional anisotropy (FA) and mean diffusivity (MD) did not significantly differ across groups, tract-specific analysis revealed that higher QRISK3 scores were significantly associated with reduced white matter integrity in the left SLF.</div></div><div><h3>Conclusion</h3><div>These findings highlight the presence of early, subclinical white matter alterations in individuals at cardio-cerebrovascular risk, even in the absence of neurological symptoms. The integration of tract-specific DTI analysis with vascular risk profiling may provide a sensitive approach for detecting preclinical CSVD and guiding early intervention strategies in at-risk populations.</div></div>","PeriodicalId":37913,"journal":{"name":"Translational Research in Anatomy","volume":"40 ","pages":"Article 100425"},"PeriodicalIF":0.0,"publicationDate":"2025-07-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144687442","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A two-trunked anatomical variance of the brachial plexus: A cadaveric case report 臂丛的两干解剖变异:一个尸体病例报告
Q3 Medicine Pub Date : 2025-07-18 DOI: 10.1016/j.tria.2025.100422
Catherine A. Cash , Camryn Buskey , Eistine Boateng , Adel Maklad , Hamoun Delaviz

Background

The brachial plexus is a network of nerves connecting five spinal nerve roots (C5-C8 and T1) and is responsible for transmitting motor and sensory signals to the upper limb. The ventral rami typically form three trunks, superior (C5-C6), middle (C7), and inferior (C8-T1), where each trunk channels motor and sensory information to specific upper limb regions.

Methods

A unique variation of the trunks of the brachial plexus was discovered during a routine dissection of a male cadaver within an anatomy laboratory.

Results

We present a case of a prefixed, two trunk brachial plexus, formed by the fusion of the middle and inferior trunks, along with downstream variations in the terminal nerve branches.

Conclusions

While anatomical variations of the brachial plexus are documented in the literature, fusion of the middle and inferior trunks are not commonly observed in human anatomy and subsequently not documented in the literature. Furthermore, we observed a prefixed plexus and anomalous communicating branches of the musculocutaneous nerve to the median nerve as additional features of the network. Altogether, understanding these variations is crucial for physicians, as it can affect surgical procedures and clinical presentations.
臂丛是连接五个脊神经根(C5-C8和T1)的神经网络,负责向上肢传递运动和感觉信号。腹侧支通常形成三条主干,上(C5-C6)、中(C7)和下(C8-T1),其中每条主干将运动和感觉信息传递到特定的上肢区域。方法在解剖实验室对一具男性尸体进行常规解剖时,发现臂丛主干有独特的变异。结果我们报告了一个由中下干融合形成的固定的双干臂丛,以及末端神经分支的下游变异。结论虽然文献记载了臂丛的解剖变异,但在人体解剖学中并不常见到中下干的融合,因此也没有文献记载。此外,我们还观察到一个固定的神经丛和肌肉皮神经与正中神经的异常交通分支作为网络的附加特征。总之,了解这些变异对医生来说是至关重要的,因为它会影响手术过程和临床表现。
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引用次数: 0
Redefining lumbosacral transitional vertebrae classification: Morphological variation in a South African population 重新定义腰骶过渡椎分类:南非人群的形态变异
Q3 Medicine Pub Date : 2025-07-17 DOI: 10.1016/j.tria.2025.100423
G.J. Paton , S. Nalla , S.A. Williams , G.J. Louw

Background

Lumbosacral transitional vertebrae (LSTV) are common anatomical variants where the last lumbar vertebra demonstrates unilateral or bilateral enlargement of the transverse processes, with articulation or fusion to the sacrum. This radio-anatomical study sought to investigate the morphological characteristics of LSTV in the South African population and describe unique variations that enhance the traditional Castellvi classification.

Methods

A retrospective radiographic review was performed on 3096 consecutive thoracoabdominal pelvic radiographs from two South African hospitals. Targeted osteological appraisal was conducted on selected skeletons containing LSTV sourced from the Raymond Dart Collection of Modern Human Skeletons. The presence of LSTV was classified according to Castellvi, identifying Types II, III, and IV, unilateral and bilateral subtypes.

Results

The prevalence of LSTV was 10 %. Morphological distribution was as follows: Type II (67.9 %), Type III (27.6 %), and Type IV (4.5 %). Subtype frequencies were IIA (41.9 %), IIB (26.0 %), IIIB (21.8 %), and IV (5.8 %). Laterality showed a predominance of bilateral cases (47.7 %), followed by left- (26.6 %) and right-sided (21.1 %) variants. Type IV morphology could not be classified by side using traditional methods. Transverse processes at the LSTV level were significantly longer than those in matched controls (p < 0.05).

Conclusion

This study proposes two refinements to the Castellvi system: First, Type IV morphology should be assigned left or right at the side of the lumbosacral fusion. Second, a novel transversoiliac articulation was associated with Type II morphology, representing a previously undescribed feature in LSTV morphology. These modifications may enhance diagnostic precision, support recognition of Bertolotti syndrome, and formulate appropriate treatment strategies.
腰骶过渡椎(LSTV)是一种常见的解剖变异,其中最后一节腰椎表现为单侧或双侧横突扩大,与骶骨关节或融合。本放射解剖学研究旨在调查南非人群LSTV的形态学特征,并描述增强传统Castellvi分类的独特变异。方法对南非两家医院连续拍摄的3096张胸腹盆腔x线片进行回顾性分析。对来自Raymond Dart Collection of Modern Human skeleton的含有LSTV的骨骼进行有针对性的骨学鉴定。根据Castellvi对LSTV的存在进行分类,分为II型、III型和IV型、单侧和双侧亚型。结果LSTV患病率为10%。形态分布为ⅱ型(67.9%)、ⅲ型(27.6%)、ⅳ型(4.5%)。亚型频次为IIA(41.9%)、IIB(26.0%)、IIIB(21.8%)和IV(5.8%)。侧侧病变以双侧病变为主(47.7%),其次为左侧病变(26.6%)和右侧病变(21.1%)。IV型形态学不能用传统方法进行侧分。LSTV水平的横突明显长于匹配对照组(p <;0.05)。本研究提出了对Castellvi系统的两种改进:首先,IV型形态学应分配在腰骶融合侧的左侧或右侧。其次,一种新的横髂关节与II型形态学有关,代表了LSTV形态学中先前未描述的特征。这些修改可以提高诊断的准确性,支持Bertolotti综合征的识别,并制定适当的治疗策略。
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引用次数: 0
Aberrant origin of left vertebral artery: A molecular embryological perspective 左椎动脉异常起源:分子胚胎学观点
Q3 Medicine Pub Date : 2025-07-11 DOI: 10.1016/j.tria.2025.100421
Connor Lee McCoy , John Joseph Cichewicz , Rainevan Miller , Soumya Sharma , Adel Maklad , Eistine Boateng

Background

Variation in the origin and course of the left vertebral artery have surgical and clinical implications in the management of medical conditions. Here, we show variant origin of the left vertebral artery in cadavers and propose potential causes for future molecular investigations.

Method

The aortic arches of 32 donors were dissected and observed for anomalous origin of the left vertebral artery in the cadaver laboratory at the University of Toledo, Ohio, USA.

Results

Out of 32 donors dissected during laboratory sessions, we observed two cases of the left vertebral artery originating directly from the aortic arch, medial to the left subclavian artery.

Conclusion

The study aims to stimulate discussions and future investigations into the molecular embryology of vasculogenesis concomitant with preconceptional and in utero exposures to understand the underlying causes of aberrant origin of the left vertebral artery. Additionally, we speculate that parental and embryonic environmental exposures influence the epigenetic landscape in germ cells and early embryos, thereby contributing to the programming of variant origin of blood vessels.
背景:左椎动脉起源和路径的变异在医疗条件的处理中具有外科和临床意义。在这里,我们展示了尸体左椎动脉的不同起源,并提出了未来分子研究的潜在原因。方法在美国俄亥俄州托莱多大学尸体实验室解剖32例供体主动脉弓,观察左椎动脉异常起源。结果在实验室解剖的32例供体中,我们观察到2例左椎动脉直接起源于主动脉弓,位于左锁骨下动脉内侧。结论本研究旨在促进对血管发生的分子胚胎学的讨论和未来的研究,以了解左椎动脉异常起源的潜在原因。此外,我们推测亲代和胚胎的环境暴露会影响生殖细胞和早期胚胎的表观遗传景观,从而促进血管变异起源的编程。
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引用次数: 0
Sex determination and stature estimation using logistic and linear regression models: A population-specific study of tibia and Fibula in Northeastern Thais 使用逻辑回归和线性回归模型的性别决定和身高估计:泰国东北部人群胫骨和腓骨的特定研究
Q3 Medicine Pub Date : 2025-07-11 DOI: 10.1016/j.tria.2025.100420
Suthat Duangchit , Chanasorn Poodendaen , Phetcharat Phetnui , Pornpimol Tasu , Worrawit Boonthai , Nareelak Tangsrisakda , Sitthichai Iamsaard

Background

Sex determination and stature estimation from skeletal remains are basic components of forensic anthropological analysis, particularly when fragmentary remains limit conventional approaches. This study aimed to establish the population-specific standards for Northeastern Thais using tibial and fibular measurements.

Materials and methods

The study examined 200 identified adult skeletons (100 males, 100 females). The nine osteometric parameters (six tibial and three fibular) were measured bilaterally. All specimens were systematically documented for age, sex, and stature.

Results

For sex determination, the results showed that univariate logistic regression models achieved the accuracy rates up to 87.50 %, with maximum proximal epiphyseal breadth of the tibia demonstrating highest discriminatory power. Multivariate approaches could significantly enhance the accuracy to 91.30 % for left tibial parameters, with age-related variation revealing optimal results in the 45–59 age group. Fibular measurements showed lower accuracy but still maintained statistical significance, particularly for fibular weight. For stature estimation, the maximum tibial length served as the most reliable univariate predictor (SEE = 6.66 cm, R = 0.572), while multivariate equations incorporating complementary parameters from both tibia and fibula improved the accuracy. Age-stratified analysis demonstrated diminished accuracy in older cohorts, especially for fibular measurements.

Conclusion

The findings align with the previous studies while reflecting distinct patterns unique to Northeastern Thai populations with their specific genetic ancestry. These population-specific equations can enhance the biological profiling capabilities in forensic investigations when the conventional methods are inapplicable due to fragmentary remains.
从骨骼遗骸中确定性别和估计身高是法医人类学分析的基本组成部分,特别是当碎片遗骸限制了传统方法时。本研究旨在通过胫骨和腓骨测量建立泰国东北部人群的特定标准。材料和方法该研究检查了200具已确认的成人骨骼(男性100具,女性100具)。测量双侧9个骨测量参数(6个胫骨和3个腓骨)。对所有标本进行了年龄、性别和身材的系统记录。结果单变量logistic回归模型的性别判别准确率高达87.50%,其中胫骨近端骨骺宽度最大具有最高的判别能力。多变量方法可以显著提高左胫骨参数的准确性,达到91.30%,年龄相关的变化显示45-59岁年龄组的最佳结果。腓骨测量的准确性较低,但仍保持统计学意义,特别是腓骨重量。对于身高估计,最大胫骨长度是最可靠的单因素预测因子(SEE = 6.66 cm, R = 0.572),而包含胫骨和腓骨互补参数的多因素方程提高了准确性。年龄分层分析表明,在老年队列中准确性降低,尤其是腓骨测量。研究结果与先前的研究一致,同时反映了泰国东北部人群独特的独特模式,具有特定的遗传血统。这些特定人群的方程可以提高法医调查的生物分析能力,当传统的方法是不适用的,由于碎片遗骸。
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引用次数: 0
Morphometric analysis of circulus arteriosus cerebri variations in a South African cadaveric sample 南非尸体样本中脑动脉循环变异的形态计量学分析
Q3 Medicine Pub Date : 2025-07-10 DOI: 10.1016/j.tria.2025.100419
Jessica Garlick, Graham Louw, Kentse Mpolokeng

Introduction

The circulus arteriosus cerebri (CAC), or Circle of Willis, exhibits significant anatomical variability, with fewer than 50 % of cases displaying the conventional configuration. CAC variations are associated with intracranial aneurysm (IA) formation and subsequent haemorrhagic stroke. Due to limited data on CAC variations in South Africa, this study aimed to assess the prevalence and types of arterial variations in a South African cadaveric sample and to document associated IAs.

Methods

This retrospective, cross-sectional and quantitative study had a sample size of 64. The CAC was dissected, removed from the base of the brain, photographed, and analysed morphologically. Variations were classified using the Ayre et al. (2021) system and recorded individually.

Results

The intact samples (n = 40) were classified according to Ayre et al. (2021) and 22.5 % of the sample displayed the conventional configuration. The predominant pattern of variation was group 5 (miscellaneous patterns), and variations were commonly observed in both the anterior and posterior circulations (55 %). Individual variations were observed (n = 64 brains; 81 variations). The leading variations were unilateral posterior communicating artery (PcoA) hypoplasia (17.3 %) and aplasia (14.8 %). The anterior communicating artery (AcoA) was the most variable artery (44.4 %), with short fusion of the anterior cerebral arteries (ACAs) being the most common variation (13.6 %) affecting the AcoA. Rare findings include type 4 and 5 PcoA terminations (double P2), not previously reported in South Africa. IA frequency was insufficient for analysis.

Conclusions

These variations may increase stroke and IA risk. Knowledge of CAC variations can support neurosurgical planning and execution. Further studies in a South African setting are recommended.
脑动脉环(CAC),或称威利斯环,具有明显的解剖变异性,只有不到50%的病例显示常规形态。CAC变异与颅内动脉瘤(IA)形成和随后的出血性中风有关。由于南非CAC变异的数据有限,本研究旨在评估南非尸体样本中动脉变异的患病率和类型,并记录相关的IAs。方法回顾性、横断面、定量研究,样本量64例。解剖CAC,从颅底取出,拍照,并进行形态学分析。使用Ayre等人(2021)的系统对变异进行分类,并单独记录。结果完整样本(n = 40)按照Ayre et al.(2021)分类,22.5%的样本显示常规配置。变异的主要模式是第5组(杂项模式),变异通常在前循环和后循环中观察到(55%)。观察到个体差异(n = 64个大脑;81变化)。单侧后交通动脉(PcoA)发育不全(17.3%)和发育不全(14.8%)居首。前交通动脉(AcoA)是最易变的动脉(44.4%),大脑前动脉(ACAs)的短融合是影响AcoA最常见的变异(13.6%)。罕见的发现包括4型和5型PcoA终止(双P2),以前未在南非报道。IA频率不足以进行分析。结论这些变异可能增加卒中和IA风险。了解CAC的变化可以支持神经外科的计划和执行。建议在南非进行进一步的研究。
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Translational Research in Anatomy
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