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目的:探讨注意缺陷多动障碍(ADHD)患儿睡眠障碍与血清铁蛋白水平的关系。方法:符合美国精神疾病诊断与统计手册第4版(DSM-Ⅳ)中ADHD诊断标准的62例6.14岁ADHD患儿,由ADHD患儿的父母填写睡眠障碍量表(SDSC),检测ADH-D患儿的血清铁蛋白水平。结果:与血清铁蛋白水平高于45/μg/L的ADHD患儿相比较,血清铁蛋白水平低于45/μg/L的ADHD患儿的SDSC“睡眠醒觉转换障碍”项评分和总分明显高于前者(P〈0.05)。2组间其他项评分比较无显著性差异(P〉0.05)。SDSC“睡眠醒觉转换障碍”项评分与血清铁蛋白水平成负相关(P〈0.05)。结论:血清铁蛋白水平低于451μg/LADHD患儿SDSC“睡眠醒觉转换障碍”(睡眠中的异常运动)的危险性显著增加。 相似文献
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注意缺陷多动障碍(Attention Deficit Hyperactivity Disorder,ADHD)是儿童期常见的一种发展性的异常,其病因及发生机理至今未明。低觉醒模型是ADHD成因的一种假设。本文从睡眠障碍导致的低觉醒探讨ADHD发生机理。通过对ADHD儿童的睡眠障碍进行分析以及将ADHD外在表现与睡眠剥夺后的表现进行对比分析,得出ADHD儿童存在的低觉醒是由于外显的或内隐的睡眠障碍引起的,一方面间接证明了低觉醒模型,另一方面为ADHD的成因研究开拓了新的思路。 相似文献
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摘要 目的:探讨艾司西酞普兰联合唑吡坦对失眠障碍患者睡眠质量、焦虑抑郁状态及血清神经递质的影响。方法:选取2018年1月~2020年12月期间我院收治的失眠障碍患者100例为研究对象。根据随机数字表法分为对照组(唑吡坦治疗,n=50)和研究组(对照组的基础上联合艾司西酞普兰治疗,n=50),比较两组患者睡眠质量、焦虑抑郁状态、血清神经递质及不良反应情况。结果:治疗4周后,研究组睡眠效率高于对照组,睡眠总时间长于对照组,醒觉时间、入睡时间短于对照组(P<0.05)。治疗4周后,研究组匹兹堡睡眠质量指数(PSQI)、汉密顿抑郁评估量表(HAMD)、汉密顿焦虑评估量表(HAMA)低于对照组(P<0.05)。治疗4周后,研究组5-羟色胺(5-HT)、r-氨基丁酸(GABA)水平高于对照组,去甲肾上腺素(NE)水平低于对照组(P<0.05)。两组不良反应发生率比较无差异(P>0.05)。结论:失眠障碍患者接受唑吡坦、艾司西酞普兰联合治疗,可有效改善患者焦虑抑郁状态、睡眠质量以及血清神经递质水平,安全性较好。 相似文献
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目的:研究微创钻孔引流术对高血压脑出血患者近期疗效及颅内感染、血肿再扩大的影响。方法:选取2017年3月至2019年2月的81例高血压脑出血患者。按照随机数表法分为观察组(n=42)和对照组(n=39),对照组采用常规开颅血肿清除术治疗,观察组采用微创钻孔引流术治疗。观察两组治疗疗效情况,血肿量、髓鞘碱性蛋白(MBP)、中枢神经特异蛋白S100水平、NIHSS、GCS评分,不良反应情况。结果:治疗后,观察组总有效率显著高于对照组[92.86%(39/42)vs69.23%(27/39)](P<0.05);血肿量、MBP、S100水平均显著低于对照组[(9.32±2.70)mL vs(15.51±3.01)mL,(3.65±0.52)μg/L vs(4.20±0.71)μg/L,(0.98±0.26)μg/L vs(1.39±0.35)μg/L](P<0.05);NIHSS评分显著低于对照组[(3.90±2.71)分vs(6.34±1.42)分](P<0.05);GCS评分显著高于对照组[(14.84±3.52)分vs(10.69±3.98)分](P<0.05);不良反应总发生率显著低于对照组[9.52%(4/42)vs38.46%(15/39)](P<0.05)。结论:微创钻孔引流术治疗高血压脑出血患者的近期疗效显著,血肿清除彻底,可有效改善脑神经缺损,减少颅内感染,促进预后恢复。 相似文献
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目的:观察鼻内镜下腺样体切除术或联合扁桃体切除术对摩洛哥儿童睡眠呼吸障碍的疗效,探讨儿童睡眠呼吸障碍治疗的手术适应症。方法:136例病例分成2组,治疗组85例睡眠呼吸障碍伴慢性扁桃体炎、或扁桃体Ⅲ°肥大的儿童,行鼻内镜下腺样体切除加扁桃体切除术;对照组51例睡眠呼吸障碍伴单纯扁桃体扁桃体Ⅱ°肥大的儿童,采用鼻内镜下腺样体切除,术后随访3个月。结果:治疗组总有效率为100%(85/85),对照组84.31%(43/51),差异有统计学意义(P0.05);两组患儿的Conners儿童行为量表评分较术前明显下降,差异有统计学意义(P0.05)。结论:鼻内镜下腺样体切除术联合扁桃体切除术,明显改善患儿睡眠和呼吸,生活质量明显提高,是治疗摩洛哥儿童睡眠呼吸障碍的一线治疗方案。 相似文献
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目的:研究血清神经元特异性烯醇化酶(NSE)、鳞状细胞癌抗原(SCCA)及癌胚抗原(CEA)在肺癌早期诊断和预后预测中的应用价值。方法:选择我院2013年1月~2017年1月收治的110例肺癌患者(肺癌组)及同期96例肺部良性疾病患者(肺良性病组)和85例门诊健康体检者(对照组)。比较各组血清NSE、SCCA及CEA水平,采用受试者工作特征(ROC)曲线分析以上指标对肺癌的诊断价值。结果:肺癌组血清NSE、SCCA、CEA水平高于肺良性病组及对照组,肺良性病组血清NSE、SCCA、CEA水平高于对照组(P<0.05)。肺癌Ⅲ+Ⅳ组血清NSE、SCCA及CEA水平高于Ⅰ+Ⅱ组(P<0.05)。小细胞肺癌组血清NSE水平高于鳞癌组、腺癌组,鳞癌组血清SCCA水平高于腺癌组及小细胞肺癌组,腺癌组血清CEA水平高于鳞癌组及小细胞肺癌组(P<0.05)。NSE<16.0μg/L者平均无疾病进展生存期(PFS)长于NSE≥16.0μg/L,SCCA<1.5μg/L者平均PFS长于SCCA≥1.5μg/L,CEA<5.0μg/L平均PFS长于CEA≥5.0μg/L(P<0.05)。NSE、SCCA和CEA及三者联合诊断肺癌的ROC曲线下面积分别为0.880、0.651、0.830及0.937,NSE+SCCA+CEA联合诊断的曲线下面积高于单个指标单独诊断(P<0.05)。结论:血清NSE、SCCA及CEA对肺癌的诊断有重要的参考价值,且有利于肺癌的分期、分型及预后评价。 相似文献
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目的:探讨多动症(ADHD)患儿血清中微量元素水平与患儿行为症状的相关性。方法:以原子吸收光谱仪检测6~14岁80名ADHD患儿及72名正常儿童血清中的铁(Fe)、锌(Zn)、铜(Cu)、钙(Ca)、镁(Mg)、镉(Cd)、铅(Pb)等微量元素的含量,应用Conner氏量表评价患儿行为症状,分析血清微量元素与行为症状评分的相关性。结果:ADHD患儿血清中Zn水平明显低于正常儿童、Pb水平明显高于正常儿童,差异均有统计学意义(P0.05);Fe、Ca略低于正常儿童,Cu、Cd略高于正常儿童,但差异均无统计学意义(P0.05)。ADHD患儿品行问题、学习问题、冲动-多动、焦虑指数较正常儿童相比有显著差异(P0.05);经Pearson相关分析,ADHD患儿血清Zn与学习问题、冲动-多动、多动指数呈负相关(P0.05),血清Pb与患儿冲动-多动、多动指数呈正相关(P0.05)。结论:ADHD患儿血清中Zn与Pb异常表达,与行为症状密切相关。在治疗ADHD患儿过程中,可以通过检测这些指标进行针对性或预防性治疗,有一定的指导价值。 相似文献
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摘要 目的:探究睡眠障碍是如何通过下丘脑-垂体-卵巢轴影响女性生育能力的。方法:选择2018年10月至2021年10月于我院妇科内分泌科就诊的育龄期女性80例作为研究对象,根据匹兹堡睡眠质量指数量表(PSQI)评估结果,将所有研究对象按照是否存在睡眠障碍分为睡眠障碍组(n=34例)和非睡眠障碍组(n=46例)。对比分析两组PSQI评分,血清性激素水平,月经周期,生育能力,通过Pearson法分析睡眠障碍与女性生育能力的相关性。结果:(1)睡眠障碍组PSQI总分以及睡眠质量、入睡时间、睡眠时间、睡眠效率、睡眠障碍和日间功能障碍各方面得分均显著高于对照组(P<0.05);(2)睡眠障碍组卵泡刺激素(FSH)、黄体生成素(LH)较非睡眠障碍组升高,而雌二醇(E2)水平低于非睡眠障碍组(P<0.05);(3)两组月经周期比较,睡眠障碍组月经紊乱比例显著高于对照组(P<0.05);(4)两组生育能力比较,睡眠障碍组生育能力显著低于对照组(P<0.05)。(5)睡眠障碍与FSH和LH均存在负相关性,和E2存在正相关(P<0.05)。结论:睡眠障碍可减弱下丘脑-垂体-卵巢轴的驱动,导致卵泡刺激素释放缓慢,延长了月经周期,并导致黄体功能下降,增加了未受孕或者再次异位妊娠的发生率。 相似文献
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目的:分析双相障碍抑郁发作及单相抑郁症患者与血清三碘甲状腺原氨酸(T3)、甲状腺素(T4)、甲状腺激素(TSH)和脑源性神经营养因子(BDNF)水平的相关性。方法:选取2017年12月~2019年12月我院收治的120例抑郁症患者为研究对象,按照病情不同分为双相障碍抑郁发作组(n=50)、单相抑郁症组(n=70),同时选取同期于本院进行体检的30例健康者作为对照组,检测血清T3、T4、TSH和BDNF水平,并进行汉密尔顿抑郁(HAMD)量表评分,分析血清T3、T4、TSH和BDNF水平的相关性。结果:双相障碍抑郁发作组起病年龄低于单相抑郁症组(P0.05);治疗前双相障碍抑郁发作组和单相抑郁症组血清T3水平高于对照组,TSH、BDNF水平低于对照组(P0.05),双相障碍抑郁发作组血清T4水平高于对照组,单相抑郁症组和对照组血清T4水平比较差异无统计学意义(P0.05),双相障碍抑郁发作组血清T4水平高于单相抑郁症组,TSH、BDNF水平低于单相抑郁症组(P0.05);治疗后双相障碍抑郁发作组和单相抑郁症组血清T4水平低于对照组,双相障碍抑郁发作组血清T4水平低于单相抑郁症组(P0.05),且三组血清T3、TSH、BDNF水平比较差异无统计学意义(P0.05);治疗后双相障碍抑郁发作组认知障碍因子评分低于单相抑郁症组(P0.05);Spearman相关分析显示,血清T3、T4、TSH水平和HAMD评分与BDNF呈负相关,TSH水平与BDNF呈正相关(P0.05)。结论:抑郁症患者血清T3、T4、TSH和BDNF水平存在异常,可作为判断双相障碍抑郁发作及单相抑郁症的指标。 相似文献
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Recent advances in the study of Kaposi's sarcoma-associated herpesvirus replication and pathogenesis
It has now been over twenty years since a novel herpesviral genome was identified in Kaposi's sarcoma biopsies. Since then, the cumulative research effort by molecular biologists, virologists, clinicians, and epidemiologists alike has led to the extensive characterization of this tumor virus, Kaposi's sarcoma-associated herpesvirus(KSHV; also known as human herpesvirus 8(HHV-8)), and its associated diseases. Here we review the current knowledge of KSHV biology and pathogenesis, with a particular emphasis on new and exciting advances in the field of epigenetics. We also discuss the development and practicality of various cell culture and animal model systems to study KSHV replication and pathogenesis. 相似文献
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RICHARD E. NORRIS 《Botanical journal of the Linnean Society. Linnean Society of London》1991,106(1):1-40
Comprises species occurring mostly in subtidal habitats in tropical, subtropical and warm-temperate areas of the world. An analysis of the type species, V. spiralis (Sonder) Lamouroux ex J. Agardh, a species from Australia, establishes basic characters for distinguishing species in the genus. These characters are (1) branching patterns of thalli, (2) flat blades that may be spiralled on their axis, (3) width of the blade, (4) primary or secondary derivation of sterile and fertile branchlets and (5) position of sterile and fertile branchlets on the thalli. Application of the latter two characters provides an important basic method for separation of species into three major groups. Osmundaria , a genus known only in southern Australia, was studied in relation to Vidalia , and its separation from the Vidalia assemblage is not accepted. Species of Vidalia therefore are transferred to the older genus name, Osmundaria. Two new species, Osmundaria papenfussii and Osmundaria oliveae are described from Natal. Confusion in the usage of the epithet, Vidalia fimbriala Brown ex Turner has been clarified, and Vidalia gregaria Falkenberg, described as an epiphyte on Osmundaria pro/ifera Lamouroux, is revealed to be young branches of the host, Osmundaria prolifera. 相似文献
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JOAN VALUÈS MONTSERRAT TORRELL NÚRIA GARCIA JACAS 《Botanical journal of the Linnean Society. Linnean Society of London》2001,137(4):399-407
Fifteen chromosome counts of six Artemisia taxa and one species of each of the genera Brachanthemum, Hippolytia, Kaschgaria, Lepidolopsis and Turaniphytum are reported from Kazakhstan. Three of them are new reports, two are not consistent with previous counts and the remainder are confirmations of very scarce (one to four) earlier records. All the populations studied have the same basic chromosome number, x = 9, with ploidy levels ranging from 2x to 6x. Some correlations between ploidy level, morphological characters and distribution are noted. 相似文献
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肝癌中HBV和HCV基因和抗原的分布及意义 总被引:1,自引:0,他引:1
采用原位分子杂交方法检测HCV
RNA及HBV X基因;采用免疫组织化学方法研究HCV核心抗原,非结构区C33c抗原及HBxAg在肝细胞肝癌中的定位及分布.结果表明(1)HCV
RNA、HBV X基因在肝细胞肝癌组织检出率分别为40%(55/136)和82%(112/136).HCV
RNA定位于癌细胞的胞浆内,阳性细胞呈散在、灶状及弥漫分布三种形式;HBV
X基因在肝癌细胞中的分布呈胞浆型、核型及核浆型,阳性细胞也呈上述三种分布形式;(2)HCV
C33c抗原、核心抗原在肝细胞肝癌中的阳性率为81%(133/164)及86%(141/164).C33c抗原定位于癌细胞及肝细胞的胞浆内;核心抗原既定位于癌细胞核中,又可定位于胞浆中.C33c抗原阳性细胞以灶状分布为主;而核心抗原阳性细 相似文献
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H.-R. GREGORIUS 《Biological journal of the Linnean Society. Linnean Society of London》1984,23(2-3):157-165
For a plant selection model with frequency-independent viabilities, fertilities and selfing rates, it is shown that apart from global fixation, for certain parameter combinations a protected polymorphism and facultative fixation (either allele may become fixed according to initial frequencies) may both occur. Facultative fixation requires different selling rates for the dominant and recessive type. Protection of the polymorphism requires resource allocation for male and female function. In this connection the problem of purely genetically caused population extinction is discussed.
For general frequency dependence and regular segregation, the chances for establishment of a completely recessive gene are compared to those of a completely dominant gene. It is proven that the process of establishment of the recessive gene, despite a fitness advantage, may be considerably endangered by drift effects if random mating prevails. The recessive gene may reach the same effectivity in establishment as a dominant gene, only if the recessive homozygote mates exclusively with its own type during the period of establishment. 相似文献
For general frequency dependence and regular segregation, the chances for establishment of a completely recessive gene are compared to those of a completely dominant gene. It is proven that the process of establishment of the recessive gene, despite a fitness advantage, may be considerably endangered by drift effects if random mating prevails. The recessive gene may reach the same effectivity in establishment as a dominant gene, only if the recessive homozygote mates exclusively with its own type during the period of establishment. 相似文献