Idiopathic normal pressure hydrocephalus (iNPH) is a potentially reversible neurological condition prevalent in the elderly, characterized by gait disturbance, cognitive decline, and urinary incontinence. Distinguishing iNPH from neurodegenerative mimics such as Alzheimer’s or Parkinson’s disease is critical to prevent missed treatment opportunities. This narrative review synthesizes current literature on the clinical presentation and diagnostic strategies for iNPH. Gait disturbance, often described as a magnetic gait, is typically the earliest sign and shows the most significant improvement following shunt surgery. Cognitive impairment manifests as frontal-subcortical dysfunction, distinct from the cortical memory deficits of Alzheimer’s disease. Diagnosis relies on integrating clinical history with specific magnetic resonance imaging findings, including disproportionately enlarged subarachnoid space hydrocephalus (DESH) and high-convexity tightness. While the cerebrospinal fluid (CSF) tap test is a valuable predictor for shunt responsiveness, clinicians must be wary of false-negative results. In addition, dopamine transporter imaging and amyloid imaging could be helpful to rule out other neurological disorders. Accurate diagnosis of iNPH requires a multidisciplinary approach combining clinical assessment, neuroimaging, and CSF dynamic evaluation. Timely identification and exclusion of comorbidities allow for effective surgical intervention, significantly reversing symptoms and improving the long-term quality of life for affected older adults.
Lee et al. (Thu,) studied this question.