Idiopathic normal pressure hydrocephalus(iNPH)is caused by impaired cerebrospinal fluid absorption in the elderly;it is a surgically treatable form of dementia.Gait disturbance,dementia,and urinary incontinence are th...Idiopathic normal pressure hydrocephalus(iNPH)is caused by impaired cerebrospinal fluid absorption in the elderly;it is a surgically treatable form of dementia.Gait disturbance,dementia,and urinary incontinence are the triad of signs for iNPH.In addition to these clinical findings,imaging studies show characteristic ventricular enlargement.High Evans Index and‘disproportionately enlarged subarachnoid hydrocephalus’are other well-known imaging findings of iNPH.If the tap test shows improved symptoms,shunt surgery is performed.The disease was first described by Hakim and Adams in 1965,followed by the publication of the first,second,and third editions of the guidelines in 2004,2012,and 2020,respectively.Recent studies signal the glymphatic system and classical cerebrospinal fluid(CSF)absorption from the dural lymphatics as aetiological mechanisms of CSF retention.Research is also underway on imaging test and biomarker developments for more precise diagnosis,shunting technique options with fewer sequelae and complications,and the influence of genetics.Particularly,the newly introduced‘suspected iNPH’in the third edition of the guidelines may be useful for earlier diagnosis.However,less well-studied areas remain,such as pharmacotherapy in non-operative indications and neurological findings other than the triadic signs.This review briefly presents previous research on these and future issues.展开更多
<b><span style="font-family:Verdana;">Object: </span></b><span style="font-family:""><span style="font-family:Verdana;">Incidence of Idiopathic ch...<b><span style="font-family:Verdana;">Object: </span></b><span style="font-family:""><span style="font-family:Verdana;">Incidence of Idiopathic chronic hydrocephalus of the adult (ICHA) is increasing in Guinea due to the aging of the population. The goal of this study was to describe its epidemiology, clinical presentation, and surgical outcome in a low-resource medical environment. </span><b><span style="font-family:Verdana;">Method: </span></b><span style="font-family:Verdana;">Sixteen patients operated for a probable ICHA were prospectively studied according to a uniform protocol</span></span><span style="font-family:""> </span><span style="font-family:""><span style="font-family:Verdana;">from June 2019 to December 2020. On computerized tomography, all operated patients had a clinical triad of gait disturbance, incontinence, dementia associated with ventriculomegaly, and transependymal edema. In addition, all patients underwent a single lumbar tap, improved clinically, and were subsequently offered a shunt consisting of a simple catheter in 37.5% and a non-adjustable high-pressure valve in 62.5%. </span><b><span style="font-family:Verdana;">Result: </span></b><span style="font-family:Verdana;">The mean age was 68.31 </span></span><span style="font-family:Verdana;">±</span><span style="font-family:""> </span><span style="font-family:Verdana;">10.4 (range 49</span><span style="font-family:""> </span><span style="font-family:Verdana;">-</span><span style="font-family:""> </span><span style="font-family:Verdana;">89). The sex ratio H/F was 1.67/1. Clinically, the most frequent comorbidity was a combination of hypertension and diabetes in 56.5% of cases.</span><span style="font-family:""> </span><span style="font-family:Verdana;">The mean time to diagnosis was 8.31 ± 2.75 months (range 3 - 14). The immediate postoperative mortality was 12.5% from a status epilepticus and pulmonary sepsis. In addition, we observed 2 cases of chronic subdural hematoma (12.5%) and 2 cases of shunt dysfunction</span><span style="font-family:""> </span><span style="font-family:Verdana;">(12.5%) in the first three months. The functional outcome was good in 23% of patients at one month (N</span><span style="font-family:""> </span><span style="font-family:Verdana;">=</span><span style="font-family:""> </span><span style="font-family:""><span style="font-family:Verdana;">13), 50% at three months (N = 10), and 87.5% at six months (N = 8). </span><b><span style="font-family:Verdana;">Conclusion: </span></b><span style="font-family:Verdana;">In carefully selected cases, the surgical outcome of ICHA in Guinea </span></span><span style="font-family:Verdana;">is</span><span style="font-family:Verdana;"> comparable to high-income countries. Efforts need to be put in helping patients get covered with universal insurance and generally promote Neurosurgery in the country to improve the quality of care.展开更多
目的系统评价蛛网膜下腔不成比例扩大的脑积水(disproportionately enlarged subarachnoid space hydrocephalus,DESH)征对特发性正常压力脑积水(idiopathic normal pressure hydrocephalus,iNPH)手术预后的诊断价值。材料与方法计算机...目的系统评价蛛网膜下腔不成比例扩大的脑积水(disproportionately enlarged subarachnoid space hydrocephalus,DESH)征对特发性正常压力脑积水(idiopathic normal pressure hydrocephalus,iNPH)手术预后的诊断价值。材料与方法计算机检索WanFang Data、CNKI、PubMed、The Cochrane Library、Web of Science和EMbase数据库,搜集DESH征诊断iNPH手术预后的诊断性试验,文献检索时限均从建库至2020年5月。由两名研究者按照纳入与排除标准进行独立筛选文献、提取资料并采用QUADAS-2工具评价纳入研究的偏倚风险后,使用Meta-Disc 1.4软件进行Meta分析。结果共纳入5个研究,包括333例患者。Meta分析结果显示:DESH征诊断iNPH的合并敏感度、特异度、阳性似然比、阴性似然比、诊断比值比和绘制汇总受试者工作特征(summary receiver operating characteristics,SROC)曲线并计算曲线下面积分别为60%[95%CI(0.54,0.67)]、66%[95%CI(0.56,0.76)],1.87[95%CI(1.13,3.10)]、0.45[95%CI(0.23,0.88)]、4.91[95%CI(1.45,16.68)]和0.75。结论本研究系统评价DESH征对iNPH手术预后的诊断价值,尽管其仅具有中等诊断价值,但仍有比较重要的临床意义,因纳入研究较少,仍需开展更多研究予以证实,同时提醒临床工作者应重视影像学尤其是核磁共振检查在iNPH诊断中的意义。展开更多
目的对特发性正常颅压性脑积水(idiopathic normal pressure hydrocephalus,iNPH)患者的认知障碍特征进行临床分析,为临床诊疗提供依据。方法通过多个量表评价23例诊断为疑似iNPH患者的认知功能,对照组为15例性别年龄匹配、经磁共振明...目的对特发性正常颅压性脑积水(idiopathic normal pressure hydrocephalus,iNPH)患者的认知障碍特征进行临床分析,为临床诊疗提供依据。方法通过多个量表评价23例诊断为疑似iNPH患者的认知功能,对照组为15例性别年龄匹配、经磁共振明确无脑积水表现的病例。采用简易精神状态检查量表评价总体认知功能,Stroop色词测验评估执行功能,听觉词语学习测验评估学习和记忆功能,数字广度测验评估注意功能,改良Rankin量表和日常生活活动能力量表评价整体生活能力。结果本研究中iNPH患者(iNPH组)的简易精神状态检查量表评分[21.00 (11.00~25.00)]较对照组[28.00(26.00~29.00)]显著下降( P <0.01);Stroop色词测验中卡片A所耗秒数[59.60(33.60~97.70)]较对照组[32.00 (26.00~39.00)]显著延长( P =0.04),卡片A正确个数[50.00 (46.00~50.00)]较对照组(均为50个)显著下降( P =0.02),完成卡片B所耗秒数[106.00(59.20~227.60)]较对照组[46.00 (37.00~50.00)]显著延长( P <0.01),完成卡片A及B总耗秒数[177.70(90.00~279.40)]较对照组[75.00 (72.00~89.00)]显著延长( P <0.01),完成卡片C所耗平均秒数[206.60(99.50~237.10)]较对照组[88.00 (70.00~120.00)]显著延长( P =0.01);听觉词语学习测验中短延迟回忆平均个数,iNPH组(4.18±2.89)较对照组(6.29±2.14)显著下降( P =0.04),长延迟回忆个数[3.50(3.00~ 5.00 )]较对照组[7.00 (6.00~9.00)]显著下降( P =0.01),线索回忆个数[1.50(0.00~4.00)]较对照组[5.50 (3.00~9.50)]显著下降( P =0.02),平均回忆总个数(即前5次回忆个数之和)[15.00(11.00~23.00)]较对照组[24.00 (20.00~37.00)]显著下降( P =0.04);数字广度测验中倒背得分(3.04± 2.12 )较对照组(4.15± 0.99 )显著下降( P =0.03);改良Rankin评分[3.00 (2.00~4.00)]较对照组(均为0分)显著增高( P <0.01);ADL评分[85.00(70.00~95.00)]较对照组(均为100分)显著下降( P <0.01)。结论iNPH患者存在认知功能下降,表现为执行功能障碍、记忆损害、注意损害及日常生活能力下降。展开更多
Idiopathic normal pressure hydrocephalus(iNPH)is a significant cause of the severe cognitive decline in the elderly population.There is no cure for iNPH,but cognitive symptoms can be partially alleviated through cereb...Idiopathic normal pressure hydrocephalus(iNPH)is a significant cause of the severe cognitive decline in the elderly population.There is no cure for iNPH,but cognitive symptoms can be partially alleviated through cerebrospinal fluid(CSF)diversion.In the early stages of iNPH,cognitive deficits occur primarily in the executive functions and working memory supported by frontostriatal circuits.As the disease progresses,cognition declines continuously and globally,leading to poor quality of life and daily functioning.In this review,we present recent advances in understanding the neurobiological mechanisms of cognitive impairment in iNPH,focusing on(1)abnormal CSF dynamics,(2)dysfunction of frontostriatal and entorhinal-hippocampal circuits and the default mode network,(3)abnormal neuromodulation,and(4)the presence of amyloid-βand tau pathologies.展开更多
Idiopathic normal pressure hydrocephalus (iNPH) is characterized by abnormal cerebrospinal fluid (CSF) flow and consequent cerebral ventricular enlargement due to imbalance of CSF production and absorption. The typica...Idiopathic normal pressure hydrocephalus (iNPH) is characterized by abnormal cerebrospinal fluid (CSF) flow and consequent cerebral ventricular enlargement due to imbalance of CSF production and absorption. The typical triad symptoms, namely cognitive decline, gait disturbance, and urinary incontinence, are thought to be caused by disruption of CSF circulation. However, some patients may still experience symptomatic progression after functional shunting, suggesting that iNPH is far more complicated than a simple disorder of CSF circulation. Moreover, the diagnostic workup of iNPH can be challenging due to symptomatic and neuroimaging overlaps with other neurological disorders, such as Alzheimer's disease. Furthermore, accumulating studies indicate that the pathogenesis of iNPH might relate to multiple mechanisms, including abnormalities of brain development, brain extracellular matrix, synaptic function, blood flow, and cerebral metabolism. Therefore, iNPH is not an isolated entity in occurrence and development. Nevertheless, different pathogeneses may result in protein content changes in CSF, and the biomarkers in CSF may reflect the possible mechanisms involving the etiology of iNPH and are potentially useful in assisting the diagnosis and treatment selection. In this review, we summarize the main findings of CSF biomarkers and aim to outline a possible synthetic profile in assisting iNPH diagnosis and therapeutic options.展开更多
Idiopathic normal pressure hydrocephalus(iNPH)is a clinical syndrome characterized by cognitive decline,gait disturbance,and urinary incontinence.As iNPH often occurs in elderly individuals prone tomany types of comor...Idiopathic normal pressure hydrocephalus(iNPH)is a clinical syndrome characterized by cognitive decline,gait disturbance,and urinary incontinence.As iNPH often occurs in elderly individuals prone tomany types of comorbidity,a differential diagnosis with other neurodegenerative diseases is crucial,especially Alzheimer’s disease(AD).A growing body of published work provides evidence of radiological methods,including multimodal magnetic resonance imaging and positron emission tomography,which may help noninvasively differentiate iNPH from AD or reveal concurrent AD pathology in vivo.Imaging methods detecting morphological changes,white matter microstructural changes,cerebrospinal fluid circulation,and molecular imaging have been widely applied in iNPH patients.Here,we review radiological biomarkers using different methods in evaluating iNPH pathophysiology and differentiating or detecting concomitant AD,to noninvasively predict the possible outcome postshunt and select candidates for shunt surgery.展开更多
文摘Idiopathic normal pressure hydrocephalus(iNPH)is caused by impaired cerebrospinal fluid absorption in the elderly;it is a surgically treatable form of dementia.Gait disturbance,dementia,and urinary incontinence are the triad of signs for iNPH.In addition to these clinical findings,imaging studies show characteristic ventricular enlargement.High Evans Index and‘disproportionately enlarged subarachnoid hydrocephalus’are other well-known imaging findings of iNPH.If the tap test shows improved symptoms,shunt surgery is performed.The disease was first described by Hakim and Adams in 1965,followed by the publication of the first,second,and third editions of the guidelines in 2004,2012,and 2020,respectively.Recent studies signal the glymphatic system and classical cerebrospinal fluid(CSF)absorption from the dural lymphatics as aetiological mechanisms of CSF retention.Research is also underway on imaging test and biomarker developments for more precise diagnosis,shunting technique options with fewer sequelae and complications,and the influence of genetics.Particularly,the newly introduced‘suspected iNPH’in the third edition of the guidelines may be useful for earlier diagnosis.However,less well-studied areas remain,such as pharmacotherapy in non-operative indications and neurological findings other than the triadic signs.This review briefly presents previous research on these and future issues.
文摘<b><span style="font-family:Verdana;">Object: </span></b><span style="font-family:""><span style="font-family:Verdana;">Incidence of Idiopathic chronic hydrocephalus of the adult (ICHA) is increasing in Guinea due to the aging of the population. The goal of this study was to describe its epidemiology, clinical presentation, and surgical outcome in a low-resource medical environment. </span><b><span style="font-family:Verdana;">Method: </span></b><span style="font-family:Verdana;">Sixteen patients operated for a probable ICHA were prospectively studied according to a uniform protocol</span></span><span style="font-family:""> </span><span style="font-family:""><span style="font-family:Verdana;">from June 2019 to December 2020. On computerized tomography, all operated patients had a clinical triad of gait disturbance, incontinence, dementia associated with ventriculomegaly, and transependymal edema. In addition, all patients underwent a single lumbar tap, improved clinically, and were subsequently offered a shunt consisting of a simple catheter in 37.5% and a non-adjustable high-pressure valve in 62.5%. </span><b><span style="font-family:Verdana;">Result: </span></b><span style="font-family:Verdana;">The mean age was 68.31 </span></span><span style="font-family:Verdana;">±</span><span style="font-family:""> </span><span style="font-family:Verdana;">10.4 (range 49</span><span style="font-family:""> </span><span style="font-family:Verdana;">-</span><span style="font-family:""> </span><span style="font-family:Verdana;">89). The sex ratio H/F was 1.67/1. Clinically, the most frequent comorbidity was a combination of hypertension and diabetes in 56.5% of cases.</span><span style="font-family:""> </span><span style="font-family:Verdana;">The mean time to diagnosis was 8.31 ± 2.75 months (range 3 - 14). The immediate postoperative mortality was 12.5% from a status epilepticus and pulmonary sepsis. In addition, we observed 2 cases of chronic subdural hematoma (12.5%) and 2 cases of shunt dysfunction</span><span style="font-family:""> </span><span style="font-family:Verdana;">(12.5%) in the first three months. The functional outcome was good in 23% of patients at one month (N</span><span style="font-family:""> </span><span style="font-family:Verdana;">=</span><span style="font-family:""> </span><span style="font-family:""><span style="font-family:Verdana;">13), 50% at three months (N = 10), and 87.5% at six months (N = 8). </span><b><span style="font-family:Verdana;">Conclusion: </span></b><span style="font-family:Verdana;">In carefully selected cases, the surgical outcome of ICHA in Guinea </span></span><span style="font-family:Verdana;">is</span><span style="font-family:Verdana;"> comparable to high-income countries. Efforts need to be put in helping patients get covered with universal insurance and generally promote Neurosurgery in the country to improve the quality of care.
文摘目的对特发性正常颅压性脑积水(idiopathic normal pressure hydrocephalus,iNPH)患者的认知障碍特征进行临床分析,为临床诊疗提供依据。方法通过多个量表评价23例诊断为疑似iNPH患者的认知功能,对照组为15例性别年龄匹配、经磁共振明确无脑积水表现的病例。采用简易精神状态检查量表评价总体认知功能,Stroop色词测验评估执行功能,听觉词语学习测验评估学习和记忆功能,数字广度测验评估注意功能,改良Rankin量表和日常生活活动能力量表评价整体生活能力。结果本研究中iNPH患者(iNPH组)的简易精神状态检查量表评分[21.00 (11.00~25.00)]较对照组[28.00(26.00~29.00)]显著下降( P <0.01);Stroop色词测验中卡片A所耗秒数[59.60(33.60~97.70)]较对照组[32.00 (26.00~39.00)]显著延长( P =0.04),卡片A正确个数[50.00 (46.00~50.00)]较对照组(均为50个)显著下降( P =0.02),完成卡片B所耗秒数[106.00(59.20~227.60)]较对照组[46.00 (37.00~50.00)]显著延长( P <0.01),完成卡片A及B总耗秒数[177.70(90.00~279.40)]较对照组[75.00 (72.00~89.00)]显著延长( P <0.01),完成卡片C所耗平均秒数[206.60(99.50~237.10)]较对照组[88.00 (70.00~120.00)]显著延长( P =0.01);听觉词语学习测验中短延迟回忆平均个数,iNPH组(4.18±2.89)较对照组(6.29±2.14)显著下降( P =0.04),长延迟回忆个数[3.50(3.00~ 5.00 )]较对照组[7.00 (6.00~9.00)]显著下降( P =0.01),线索回忆个数[1.50(0.00~4.00)]较对照组[5.50 (3.00~9.50)]显著下降( P =0.02),平均回忆总个数(即前5次回忆个数之和)[15.00(11.00~23.00)]较对照组[24.00 (20.00~37.00)]显著下降( P =0.04);数字广度测验中倒背得分(3.04± 2.12 )较对照组(4.15± 0.99 )显著下降( P =0.03);改良Rankin评分[3.00 (2.00~4.00)]较对照组(均为0分)显著增高( P <0.01);ADL评分[85.00(70.00~95.00)]较对照组(均为100分)显著下降( P <0.01)。结论iNPH患者存在认知功能下降,表现为执行功能障碍、记忆损害、注意损害及日常生活能力下降。
基金supported by the National Natural Science Foundation of China(31961133025).
文摘Idiopathic normal pressure hydrocephalus(iNPH)is a significant cause of the severe cognitive decline in the elderly population.There is no cure for iNPH,but cognitive symptoms can be partially alleviated through cerebrospinal fluid(CSF)diversion.In the early stages of iNPH,cognitive deficits occur primarily in the executive functions and working memory supported by frontostriatal circuits.As the disease progresses,cognition declines continuously and globally,leading to poor quality of life and daily functioning.In this review,we present recent advances in understanding the neurobiological mechanisms of cognitive impairment in iNPH,focusing on(1)abnormal CSF dynamics,(2)dysfunction of frontostriatal and entorhinal-hippocampal circuits and the default mode network,(3)abnormal neuromodulation,and(4)the presence of amyloid-βand tau pathologies.
文摘Idiopathic normal pressure hydrocephalus (iNPH) is characterized by abnormal cerebrospinal fluid (CSF) flow and consequent cerebral ventricular enlargement due to imbalance of CSF production and absorption. The typical triad symptoms, namely cognitive decline, gait disturbance, and urinary incontinence, are thought to be caused by disruption of CSF circulation. However, some patients may still experience symptomatic progression after functional shunting, suggesting that iNPH is far more complicated than a simple disorder of CSF circulation. Moreover, the diagnostic workup of iNPH can be challenging due to symptomatic and neuroimaging overlaps with other neurological disorders, such as Alzheimer's disease. Furthermore, accumulating studies indicate that the pathogenesis of iNPH might relate to multiple mechanisms, including abnormalities of brain development, brain extracellular matrix, synaptic function, blood flow, and cerebral metabolism. Therefore, iNPH is not an isolated entity in occurrence and development. Nevertheless, different pathogeneses may result in protein content changes in CSF, and the biomarkers in CSF may reflect the possible mechanisms involving the etiology of iNPH and are potentially useful in assisting the diagnosis and treatment selection. In this review, we summarize the main findings of CSF biomarkers and aim to outline a possible synthetic profile in assisting iNPH diagnosis and therapeutic options.
基金Thisworkwas supported by the National Natural Science Foundation of China(no.82071203)Science and Technology Innovation 2030“Brain Science and Brain-inspired Research”Youth Scientist Program(no.2022ZD0213600)+1 种基金Natural Science Foundation of Sichuan(no.2022NSFSC1325)Chengdu Science and technology Bureau Program(no.2019-YF09-00215-SN)。
文摘Idiopathic normal pressure hydrocephalus(iNPH)is a clinical syndrome characterized by cognitive decline,gait disturbance,and urinary incontinence.As iNPH often occurs in elderly individuals prone tomany types of comorbidity,a differential diagnosis with other neurodegenerative diseases is crucial,especially Alzheimer’s disease(AD).A growing body of published work provides evidence of radiological methods,including multimodal magnetic resonance imaging and positron emission tomography,which may help noninvasively differentiate iNPH from AD or reveal concurrent AD pathology in vivo.Imaging methods detecting morphological changes,white matter microstructural changes,cerebrospinal fluid circulation,and molecular imaging have been widely applied in iNPH patients.Here,we review radiological biomarkers using different methods in evaluating iNPH pathophysiology and differentiating or detecting concomitant AD,to noninvasively predict the possible outcome postshunt and select candidates for shunt surgery.