壁面厚度对一体化小腿假肢应力分布的影响

一体化假肢是以聚合物为材料从接受腔到假腿一体成型的新型下肢假肢 ,它比传统型假肢更经济、美观、轻便 ,具有较大的应用前景。如同传统假肢 ,应力分析对于一体化假肢的构型设计和优化具有重要的意义。由于假肢中的应力大小及分布与其所用材料的力学特性密切相关。本文的工作是基于一实验用内骨架一体化小腿假肢的真实几何构型 ,考虑残端软组织和骨 ,建立一体化小腿假肢的三维有限元模型 ;在保持假肢的几何形状不变的前提下 ,建立三个不同壁面厚度的一体化小腿假肢的三维模型 ,应用有限元分析方法 ,计算这些模型在模拟 Heel Off步态时相的载荷作用下的应力分布 ,分析壁面厚度对一体化小腿假肢应力分布的影响 ,为一体化小腿假肢壁面厚度的设计标准提供参考。结果表明 ,可以通过适当增加壁面厚度来减小一体化假肢的应力及软组织表面的压力。     

小腿假肢接受腔计算机三维模型的构建

背景:假肢接受腔作为截肢患者肢体残端和假肢之间载荷传递的惟一通道,是影响假肢适配性的重要部件。假肢接受腔的三维建模是接受腔实用性的关键,可以在测量时得到更准确的数据。目的:建立假肢接受腔计算机三维模型,为接受腔有限元分析提供数据基础,为加工制造接受腔提供可靠的参数。方法:选择1例32岁右侧小腿截肢的男性患者,髋关节各肌力正常,髋18°屈曲挛缩,其他关节活动度正常。根据患者CT和核磁共振扫描图像,采用Mimics10.0软件处理数据,构建假肢接受腔计算机三维模型,准确模拟残肢和接受腔的结构。结果与结论:建立的小腿残肢和接受腔计算机三维模型比较准确地反映了接受腔和残肢的几何特征和外部轮廓。假肢接受腔三维模型的建立有助于提高制作的成功率,从根本上改变传统依靠手工设计、测量、取型、修型等落后的生产模式。     

假肢接受腔设计及界面应力的有限元分析

文题释义： Mimics 10.0软件：作为专业的三维图像处理软件,能将CT图像转化为残肢的三维模型,计算机生成的三维模型与患者的实际尺寸基本无差别。 有限元分析：是利用数学近似的方法对真实物理系统(几何和载荷工况)进行模拟的方法。 背景：残肢-接受腔界面生物力学特性不仅对假肢的适配性有着直接影响,而且也是对接受腔结构进行优化设计的基础。将数字化设计技术与康复工程结合在一起,将有效地提髙假肢接受腔的制作效率和质量。 目的：采用逆正向结合的建模方法,对小腿截肢患者进行定制式的接受腔模型设计,评估残肢与接受腔的界面应力,对接受腔进行迭代设计,优化后的模型采用3D打印制作,以改善传统手工制作接受腔方法。 方法：选择2例内蒙古自治区荣誉军人肢残康复中心的小腿截肢志愿者,根据患者残肢的CT扫描图像,采用Mimics进行图像处理,然后经过Geomagic和UG逆向得到残肢的几何模型。通过使用计算机辅助设计软件Fusion360,根据残肢各个部位的组织结构不同的承受能力作为修型原理对接受腔进行正向建模设计。选用Mooney-Revlin超弹性模型定义软组织的材料特性,对残肢-接受腔界面应力进行有限元分析,并根据结果反馈指导对接受腔进行迭代设计,对再次修型后的接受腔模型进行评估。3D打印制作出接受腔,并进行实验测量。 结果与结论：①对迭代设计后的接受腔与残肢界面的应力进行分析,得到残肢各区域的应力值均低于疼痛阈值,符合设计标准,能较好实现功能传递性和安全舒适性;②此2例患者穿戴3D打印制作的接受腔适配性、稳定性良好,步行对称性相比手工制作接受腔均有显著改善,满足残肢生物力学要求;③试验建立了完整的假肢接受腔的设计、评估及制造系统。 ORCID: 0000-0002-8570-9689(王晓辉) 中国组织工程研究杂志出版内容重点：人工关节;骨植入物;脊柱;骨折;内固定;数字化骨科;组织工程     

小腿残肢与接受腔的非线性有限元分析

目的研究残肢与接受腔生机界面力学特性及残端应力情况,为设计和优化小腿接受腔结构、提高其佩戴舒适性提供理论依据。方法针对释压稳定(compression-release stabilization,CRS)接受腔,采用有限元软件ABAQUS分析残肢与CRS接受腔界面应力分布情况,软组织采用非线性超弹性材料Mooney-Rivlin本构模型,得到静止站立中期残肢与CRS接受腔接触界面正应力和剪切应力分布情况,并相应建立髌韧带承重(patellar tendon bearing,PTB)小腿接受腔三维有限元模型,将两者结果进行比较。结果残肢与CRS接受腔界面应力主要分布在胫骨内侧、胫骨外侧和后肌群等承重区,与PTB接受腔模型主要受力区域相似,CRS接受腔残肢末端平均界面应力较PTB接受腔高19 kPa。结论 CRS接受腔具有较好的透气性且应力分布较合理,接受腔形状的不同可改变残肢与接受腔生机界面应力分布,优化其设计有助于提高假肢穿戴舒适性。     

内骨架一体化小腿假肢的生物力学研究

一体化假肢是以聚合物为材料从接受腔到假腿一体成型的新型下肢假肢，它比传统型假肢更经济、美观、轻便，具有较大的应用前景。目前的相关研究主要集中在设计与制作及少量的临床研究方面。由于一体化假肢与传统型假肢在结构上的差异，有必要对其进行应力分析。本研究的目的是开展内骨架一体化假肢的生物力学研究，本研究基于内骨架一体化小腿假肢的真实几何构型，建立三维有限元模型，计算该模型在模拟Heel OH步态时相的载荷作用下的应力分布；在保持该模型的几何形状不变的情况下，建立了三个不同壁面厚度的一体化小腿假肢的有限元模型，分析壁面厚度对一体化小腿假肢应力分布的影响；通过分别赋予模型四种不同高分子聚合物的材料力学特性值，分析不同材料的一体化假肢的应力分布特点；分别对模型施加与正常步态的五个典型时相对应的载荷，分析一体化小腿假肢在各步态时相的应力分布特点。本研究结果对一体化假肢设计有指导价值。     

一体化小腿假肢的三维有限元应力分析

建立一体化小腿假肢和残肢的三维模型，应用有限元分析方法，计算此模型在模拟Mid—Stance步态时相的载荷作用下各节点的应力，从而得到此模型内外表面的应力分布，为一体化假肢设计的CAD＼CAM系统提供理论依据。计算结果表明，接受腔的应力值较小，假腿的应力值较大，高应力区出现在假腿下端及接受腔与假腿的交界区域。     

髋离断假肢接受腔-残肢站立期静态有限元分析

目的 利用有限元分析方法研究髋残肢在支撑阶段与髋离断假肢接受腔生机界面的力学特性,为优化、设计髋接受腔结构提供理论依据,为评估髋接受腔舒适度提供研究基础。方法 根据患者残肢CT扫描模型,采用逆向建模的方式,三维重建骨骼、软组织以及接受腔模型。利用有限元方法 研究站立状态下残肢-髋接受腔界面正应力及剪切应力的分布情况,并通过设计压力采集模块系统进行验证。结果 残肢与髋接受腔界面应力主要分布在腰部和残肢底部,位于残肢其余区域的界面应力则分布较为均匀。有限元计算结果和压力采集模块系统测量结果 有较好的符合。结论 为能较好实现髋接受腔功能传递性和安全舒适性,需要充分考虑残肢腰部和底部的受力以及残肢与接受腔的配合度。     

大腿假肢支撑期有限元分析

目的分析大腿截肢患者的硅胶套材料属性,对支撑期残肢与接受腔之间接触面的力学分布的影响,为大腿假肢适配方案中硅胶套的选取提供参考。方法利用计算机断层扫描技术获取大腿截肢患者残端与接受腔的断层图像,通过影像学信息和工程学方法,分别获取接受腔、硅胶套、残肢、骨骼等结构的三维模型;根据角度变化调整模型,获得初始接触期、负荷反应期、站立中期、站立末期、摆动前期5个时相的组装模型;根据三维动作捕捉系统Motion和Kistler三维测力平台测得的地面反作用力及髋关节角度变化的结果,对5个时相下大腿假肢模型分别进行有限元非线性接触分析;在此基础上,模拟分析了硅胶套不同弹性模量的变化对残肢表面等效应力以及剪切应力分布的影响。结果穿戴不同弹性模量的硅胶套时,残肢所受最大等效应力以及最大剪切应力在初始接触期、负荷反应期、站立中期、站立末期时相时出现在残肢内侧和接受腔口型边缘对应的残肢位置,在摆动前期时相时则出现在残肢内侧、接受腔口型边缘对应的残肢位置和坐骨周围等位置。当硅胶套弹性模量在0.98~2.70 MPa范围内变化时,在摆动前期残肢所受等效应力变化范围为13.85~23.55 k Pa,最大剪切应力变化范围为7.82~13.46 k Pa,而其他时相基本一致。结论硅胶套的力学特性影响大腿假肢残肢与接受腔之间接触面的受力分布,摆动前期残肢所受最大等效应力与最大剪切应力随硅胶套弹性模量变化大,在实际适配过程中需注意。     

小腿假肢接受腔的三维有限元分析

通过建立三维非线性有限元模型来分析小腿假肢接受腔与残肢之间的载荷分布。此模型基于残肢,骨头,软套和接受腔的三维几何形状,考虑界面摩擦滑动条件和软组织的大变形等非线性因素。模型可以预测不同外载下残肢和接受腔之间的压力,剪切力和相对滑动情况。并分析了不同的接受腔形状对载荷分布的影响。     

基于生物力学信息数字化机器人辅助手术系统

目的 建立一套数字化机器人辅助手术系统再现真实手术过程,并通过仿真系统与外部力反馈设备的结合实现对虚拟环境中机器人的控制和力觉反馈。方法 系统的设计包括：基于生物力学理论的人体组织建模、基于有限元方法人体组织生物力学模型的计算、外部力反馈设备的设计、控制算法设计等。通过多层次模型、系统集成等方法,实现基于生物力学信息并具有交互特性的虚拟机器人辅助骨折牵引复位手术平台。结果 当主手控制系统和虚拟环境生成机通过局域网连接成功后,该系统完成了闭环信息传递过程。结论 该系统可以实现对虚拟环境中手术机器人的主从控制、视觉反馈和力觉反馈。该项研究为数字化模拟外科手术相关技术的发展起到推进作用,模拟手术在提高手术成功率、新医生的培训方面具有很强的优势。     

The universal muscular chain reaction,muscle spasm,Torsions, ruptures and extravasations. Chameleons of pathology and some manifestations of simple muscular disorders

Most bodily functions require the coordinated actions of complementary and supplementary paired muscle groups. Where this essential muscular cooperation is lacking, hollow organs may burst and others become literally screwed up, giving rise to many similar spastic diseases such as Torticollis, Twisted ovarian cyst, Torsion of the Testis, Volvulus of the intestines, Varicose Veins, Megacolon, Aortamegaly, Scoliosis, Erb's Palsy, Peyronie's Disease, Main-en-Griffe, Undescended Foot (Pes Cavus), Talipes, Strabismus. Spasm is “panenepidemic” and unclassified examples of Torsion Dystonia and Dyskinesia really are as common as debt and taxes.     

Studien zur humoralen Regulation des erythropoetischen Proliferationsspeichers beim Menschen

Zusammenfassung Die Beeinflussung der Erythroblasten-Proliferation durch das Mikromilieu wurde in vitro mittels Auswertung durch Differential- und Mitosezählungen und Signifikanzberechnung vieler Versuchsreihen auch unter verschiedenen pathologischen Bedingungen getestet.Sowohl die Mitosehäufigkeit wie die Ausreifung waren positiv mit dem Erythropoetingehalt des Medium korreliert. Der Effekt wurde durch Folsäure, Ätiocholanolon und cAMP verstärkt. Cobalt stimulierte ebenso wie Testosteron und Methenolon in vitro unabhängig von der Erythropoetinkonzentration im Medium die Erythroblastenproliferation. Ein vermindertes Eisenangebot störte die endgültige Ausreifung der Erythroblasten zu Retikulozyten und bewirkte dadurch eine Ineffektivität der Erythorpoese. Anhaltspunkte für ein Erythrozyten-Chalon oder einen Erythropoetinhemmkörper ließen sich aus unserem Versuchsansatz nicht gewinnen, weil er die Transformation der pluripotenten in die erythropoetin-sensible Stammzelle nicht einschließt. Als Nebenbefund ergab sich eine Stimulation des granulozytopoetischen Proliferationsspeichers durch Serumzusatz zum Medium von Patienten nach akutem Blutverlust und bei Polycythämia vera.Unterstützt durch die Deutsche Forschungsgemeinschaft     

HLA study in Amerindian Bolivia La Paz Aymaras

Aymara people has been a relatively homogeneous group since Spanish Conquest by 1,532 CE, even if previously represented a group of various cultural defined populations who gave rise to them. They were and are established in Andean Altiplano around Titikaka Lake (Bolivia, Peru), Argentina and Chile neighborhood, speak Aymara language and have been maintained after Europeans arrival at a lower social status than Quechua (Inca) speaking people. However, both Aymara and Quechua populations acknowledge Titikaka Lake as center of their origins; both languages are also related. Specific high frequencies of HLA-A*02, -A*24 and -A*68, HLA-B*35, -B*39 and -B*48, HLA-DRB1*08:02, -DRB1*09:01, and -DRB1*14:02, and HLA-DQB1*04:02, -DQB1*03:02 and -DQB1*03:01 alleles are found in Aymaras and HLA class II haplotypes common to Andean Amerindians (DRB1*08:02-DQB1*04:02 and DRB1*04:03-DQB1*03:02), like Quechua, Aymara, Uros, Lamas and Mapuche are also found in Easter and other Pacific Islands. Giant human head stone statues at Tiwanaku (Titikaka Lake, Bolivia) are also found at Easter Island. Thus, it is possible a gene and cultural flow between Andean Amerindians and Easter and other Pacific Islands, as it was demonstrated by Thor Heyerdahl in his Kon-Tiki expedition which reached Pacific Islands sailing from El Callao Harbour (Lima, Peru).     

Hypo- und Hypermagnesämie aus kardiologischer Sicht

Zusammenfassung Eine Reihe pathologischer Zustände bedingen Magnesiummangel. Zustände mit Hypermagnesämie sind ebenfalls bekannt, doch wesentlich seltener. Für den Kardiologen beachtenswert ist, daß unter Therapie mit bestimmten Diuretica bei Herzinsuffizienz, bei Herzinfarkt, Kardiomyopathie, Digitalisintoxikation und bestimmten Herzrhythmusstörungen Hypomagnesämie beobachtet wurde. Leider kann in der klinischen Routine nur ein extracelluläres Magnesiumdefizit durch Serumbestimmungen gemessen werden; über Magnesiummangel einzelner Organe kann nichts ausgesagt werden. Hinweise für Magnesiummangel geben aber neben der Messung des Serumspiegels Anamnese, klinischer Befund, bestimmte EKG-Veränderungen wie auch evtl. Hypokalämie, ein Zustand, bei dem sich oft — besonders bei Aldosteronismus — parallele Veränderungen zeigten.Tierexperimente deuten darauf hin, daß infarktähnliche Läsionen unter Magnesiummangel entstehen, doch ob Herzinfarkt beim Menschen durch Magnesiummangel ausgelöst werden kann, ist noch ungeklärt. In Leichenherzen zeigte sich im Infarktgebiet neben Calciumakkumulation signifikanter Magnesiumverlust, wobei unklar blieb, ob sich Ursache oder Folge des Infarktes widerspiegelten. Falls ein ursächlicher Zusammenhang besteht, ist er im Myokardstoffwechsel selbst zu suchen, wie bei der Alkoholkardiomyopathie, wo myokardialer Magnesiummangel zumindest als pathogenetischer Teilfaktor anerkannt wird. Andererseits versucht man aber auch Beziehungen zwischen Atherosklerose, Blutgerinnung und Hypomagnesämie herzustellen, in der Meinung, daß Magnesiummangel auch über den coronaren Pathomechanismus des Herzinfarktes wirken könnte. Sicher scheint, daß gewisse EKG-Veränderungen und Herzrhythmusstörungen durch einen irritierten Magnesiumhaushalt bedingt sein können, da sie bei Gabe bzw. Entzug von Magnesium verschwinden. Daß Magnesiummangel die Glykosidtoleranz verringert, wird tierexperimentell bestätigt. Unter Hypomagnesämie bewirkt Acetylstrophanthidin eher und länger Rhythmusstörungen als ohne, außerdem lassen diese sich durch Magnesiumgaben eliminieren. Da in gewissen Fällen spontane und digitalisinduzierte Herzrythmusstörungen durch Magnesiuminjektionen beseitigt wurden, scheint Magnesium als Therapeuticum angebracht. Einsatz verschiedener Magnesiumsalze bei Angina pectoris, degenerativen Herzerkrankungen und Herzinsuffizienz ohne geprüften und offensichtlich gestörten Magnesiumhaushalt ist fragwürdig, weil keine eindeutigen klinischen Erfolgsbeweise vorliegen. Immerhin mag es aber larvierte, durch Serumbestimmungen nicht erfaßbare Mangelzustände geben. Allgemein erscheint es aus kardiologischer Sicht ratsam, den Magnesiumhaushalt zu überwachen und in entsprechenden Fällen auszugleichen, um möglichen Myokardläsionen oder fatalen Herzrhythmusstörungen entgegenzuwirken.     

Lipid composition of metacestodes of Taenia taeniaeformis and lipid changes during growth

A lipid analysis was performed on developing metacestodes of Taenia taeniaeformis removed from the livers of rats at times varying from 3 to 35 weeks post infection. Lipid accounted for 7–21% of the dry weight of the parasites. The highest proportions were found at the earlier stages. The distribution was as follows; neutral lipid 27–45%; glycolipid 5–11%; and phospholipid 50–61%. The major neutral lipid was cholesterol, and minor neutral lipids were sterol esters, triglycerides, diglycerides and monoglycerides. Hydrocarbons were present throughout development, but in the highest amounts at the earlier stages. Five different glycolipids were found, all of which were identified as glycosphingolipids. An increase in the proportion of more complex glycolipids was noted as parasites grew older. Ten different phospholipids were identified, with the major components being phosphatidylcholine, phosphatidylethanolamine, and phosphatidylserine. Other phospholipids were: lysophosphatides, phosphatidylinositol, phosphatidic acid, diphosphatidylglycerol, sphingomyelin, and an unknown phospholipid component. Changes in the relative amounts of the two major phospholipids were found when the early and late stages were compared. Two lipids found throughout development were identified as glycosylated dolichol phosphates, and they comprised between 1 and 3% of the total phospholipid fraction. Nineteen fatty acids were detected, and the fatty acid distribution for each lipid class at each stage was determined. Seven major fatty acids were common to each. These were: hexadecanoic, octadecanoic, oleic, linoleic, arachidonic, docosanoic, and docosahexaenoic.     

Environmental risk factors and their role in the management of atopic dermatitis

Introduction: The etiology of atopic dermatitis (AD) is multifactorial with interaction between genetics, immune and environmental factors.

Areas covered: We review the role of prenatal exposures, irritants and pruritogens, pathogens, climate factors, including temperature, humidity, ultraviolet radiation, outdoor and indoor air pollutants, tobacco smoke exposure, water hardness, urban vs. rural living, diet, breastfeeding, probiotics and prebiotics on AD.

Expert commentary: The increased global prevalence of AD cannot be attributed to genetics alone, suggesting that evolving environmental exposures may trigger and/or flare disease in predisposed individuals. There is a complex interplay between different environmental factors, including individual use of personal care products and exposure to climate, pollution, food and other exogenous factors. Understanding these complex risk factors is crucial to developing targeted interventions to prevent the disease in millions. Moreover, patients require counseling on optimal regimens for minimization of exposure to irritants and pruritogens and other harmful exposures.     

Simple Serological Assays for Detecting Rice Tungro Viruses

An attempt was made to produce sensitive and specific polyclonal antisera against the viruses causing rice tungro disease, and to assess their potential for use in simple diagnostic tests. Using a multiple, sequential injection procedure, seven batches of polyclonal antisera against rice tungro bacilliform virus (RTBV) and rice tungro spherical virus (RTSV) were produced. These were characterized for their sensitivity and specificity using ring-interface precipitin test and double antibody sandwich (DAS) ELISA. Thirty-one weeks after the first immunization, antiserum batch B6b for RTBV showed the highest ring interface titer (DEP = 1:1920). For RTSV, batches S3, S4b and S5b all had similar titres (DEP = 1:640). In DAS-ELISA, however, significant differences among purified antisera (IgG) batches were observed only at IgG dilution of 10^-3. At that dilution, IgGB4b showed the greatest sensitivity, while IgGS3 showed greatest sensitivity for RTSV. When all IgG batches were tested against 11 tungro field isolates (dual RTBV-RTSV infections) at sample dilution of 1:10, IgGB4b and IgGB6b for RTBV and IgGS3 and IgGS6b for RTSV performed equally well. However, after cross adsorption with healthy plant extracts in a specially prepared healthy plant-Sepharose affinity column, only IgGB6b could be used specifically to detect RTBV in a simple tissue-print assay.     

Is it worthy to take full-course immunotherapy for allergic rhinitis? About efficacy biomarker of allergen immunotherapy

Nowadays, people pay more attention to biomarkers that can predict clinical efficacy of immunotherapy for allergic rhinitis. As the only recognized aetiological treatment, the efficacy of allergen immunotherapy (AIT) has been proved by many studies. However, treatment success depends on compliance and persistence greatly, which can be impaired by the lengthy duration of AIT and socioeconomic status of patients. Besides, ineffectiveness is another factor that accounts for non-adherence. If the clinical efficacy can be predicted in the early stage of immunotherapy, it can help patients choose appropriate treatment plans, increase patient compliance and optimize the allocation of medical resources. This paper mainly focuses on five candidate biomarkers, the sIgE/tIgE ratio before treatment, serum inhibitory activity for IgE, decreased basophil activation, upregulation of Tregs and tolerogenic DCs, reviews the time when potential biomarkers can predict or monitor the efficacy of AIT, discusses the reason why these indicators could serve as efficacy biomarkers and interactions among potential biomarkers.     

Neurotransmitter signaling pathways required for normal development in Xenopus laevis embryos: a pharmacological survey screen

Neurotransmitters are not only involved in brain function but are also important signaling molecules for many diverse cell types. Neurotransmitters are widely conserved, from evolutionarily ancient organisms lacking nervous systems through man. Here, results are reported from a loss‐ and gain‐of‐function survey, using pharmacological modulators of several neurotransmitter pathways to examine possible roles for these pathways in normal embryogenesis. Applying reagents targeting the glutamatergic, adrenergic and dopaminergic pathways to embryos of Xenopus laevis from gastrulation to organogenesis stages, we observed and quantified numerous malformations, including craniofacial defects, hyperpigmentation, muscle mispatterning and miscoiling of the gut. These data implicate several key neurotransmitters in new embryonic patterning roles, reveal novel earlier stages for processes involved in eye development, suggest new targets for subsequent molecular‐genetic investigation, and highlight the necessity for in‐depth toxicology studies of psychoactive compounds to which human embryos might be exposed during pregnancy.     

HLA genes in Amerindians from Mexico San Vicente Tancuayalab Teenek/Huastecos

Huastecos or Teenek Amerindians are presently living at North East Mexico (San Luis Potosi State). They have probably one of the most ancient culture of Mexico and Central America together with Mayas and Olmec groups with which also show close relationships. Proximity to Atlantic Ocean/Mexican Gulf originated that Spaniards had very early contact with them at about 1519 CE or before. In the present paper we have aimed to study HLA gene profile which may be useful for HLA and disease epidemiology and transplant programs in Teeneks. HLA-DRB1*04:07, -DRB1*14:06 and -DRB1*04:11 have been found in high frequency like in other Amerindian groups. High frequency typical Amerindians HLA extended haplotypes have been found, such as A*02-B*35-DRB1*04:07-DQB1*03:02; A*68-B*39-DRB1*04:07-DQB1*03:02 and A*02-B*39-DRB1*04:07-DQB1*03:02; also new haplotypes have been described, like A*02-B*52-DRB1*04:11-DQB1*03:02, A*68-B*35-DRB1*14:02-DQB1*03:01 and A*68-B*40-DRB1*16:02-DQB1*03:01. Genetic proximity is observed not only to linguistically close Mayans, but also to Mazatecans, Mixtecans and Zapotecans, who speak an altogether different languages; it shows once more that genes and languages do not correlate. This population was greatly diminished after European contact between 1500 and 1600 years CE; in fact, North and South America First Inhabitants population was brought from 80 down to 8 million people because of diseases (i.e.: measles, smallpox or influenza), slavery and war.