Nawaiseh Mohammed B, Yassin Ahmed M, Al-Sabbagh Mohammed Q, AlNawaiseh Ahmad, Zureigat Hadil, Aljbour AlMajali Dina, Haddadin Rund R, El-Ghanem Mohammad, Abu-Rub Mohammad
Department of Ophthalmology (MBN), Jordanian Royal Medical Services, Amman; Department of Neurology (AMY), Jordan University of Science and Technology, Irbid, Jordan; Department of Neurology (MQAS), Kansas University Medical Center, Kansas City; Department of Internal Medicine (AA), St. Elizabeth's Medical Center, Boston, MA; Department of Internal Medicine (HZ), Cleveland Clinic, OH; Department of Internal Medicine (DAA), Henry Ford Health System, Detroit, MI; Department of Internal Medicine (RRH), JCESOM, Marshall University, WV; Department of Clinical Sciences (ME-G), College of Medicine, University of Houston, HCA Northwest Medical Center, Houston, TX; and Department of Neurology (MA-R), George Washington University, Washington, DC.
Neurol Clin Pract. 2024 Feb;14(1):e200215. doi: 10.1212/CPJ.0000000000200215. Epub 2023 Nov 10.
Patients with sickle cell disease (SCD) are prone to symptomatic neurologic complications. Previous studies reported accrual of neural injury starting at early age, even without having symptomatic neurologic events. The aim of this study was to assess the prevalence and risk factors of abnormal neurologic findings in patients with SCD with no history of major symptomatic neurologic events.
Our study extracted patients diagnosed with SCD from the Cooperative Study of Sickle Cell Disease. Patients who underwent a neurologic evaluation were included in our analysis. Patients with previous documented major symptomatic neurologic events were excluded. We compared patients with SCD with abnormal neurologic findings with those without in terms of clinical and laboratory parameters using multivariate binary logistic regression.
A total of 3,573 patients with SCD were included (median age = 11 [IQR = 19] years, male = 1719 [48.1%]). 519 (14.5%) patients had at least one abnormal neurologic finding. The most common findings in descending order were abnormal reflexes, gait abnormalities, cerebellar dysfunction, language deficits, nystagmus, abnormal muscle tone and strength, Romberg sign, Horner syndrome, and intellectual impairment. History of eye disease (odds ratio [OR] = 2.76, 95% confidence interval [CI] = 1.63-4.68) and history of osteomyelitis (OR = 2.55, 95% CI 1.34-4.84) were the strongest predictors of abnormal neurologic findings, followed by smoking (OR = 1.59, 95% CI 1.08-2.33), aseptic necrosis (OR = 1.57, 95% CI 1.06-2.33), hand-foot syndrome (OR = 1.48, 95% CI 1.04-2.12), and male sex (OR = 1.42, 95% CI 1.01-2.02).
Neurologic deficits are relatively common in patients with SCD, even without documented major neurologic insults. They range from peripheral and ophthalmic deficits to central and cognitive disabilities. Patients with SCD should have early regular neurologic evaluations and risk factor modification, particularly actively promoting smoking cessation.
镰状细胞病(SCD)患者易出现有症状的神经并发症。既往研究报道,神经损伤从早年就开始累积,即使没有出现有症状的神经事件。本研究的目的是评估无重大有症状神经事件病史的SCD患者神经学异常表现的患病率及危险因素。
我们的研究从镰状细胞病合作研究中提取诊断为SCD的患者。接受神经学评估的患者纳入我们的分析。排除既往有记录的重大有症状神经事件的患者。我们使用多变量二元逻辑回归,比较有神经学异常表现的SCD患者与无异常表现的患者在临床和实验室参数方面的差异。
共纳入3573例SCD患者(中位年龄 = 11岁[四分位间距 = 19岁],男性 = 1719例[48.1%])。519例(14.5%)患者至少有一项神经学异常表现。按降序排列,最常见的表现为反射异常、步态异常、小脑功能障碍、语言缺陷、眼球震颤、肌张力和肌力异常、闭目难立征、霍纳综合征及智力障碍。眼部疾病史(比值比[OR] = 2.76,95%置信区间[CI] = 1.63 - 4.68)和骨髓炎病史(OR = 2.55,95% CI 1.34 - 4.84)是神经学异常表现最强的预测因素,其次是吸烟(OR = 1.59,95% CI 1.08 - 2.33)、无菌性坏死(OR = 1.57,95% CI 1.06 - 2.33)、手足综合征(OR = 1.48,95% CI 1.04 - 2.12)及男性(OR = 1.42,95% CI 1.01 - 2.02)。
神经功能缺损在SCD患者中相对常见,即使没有记录到重大神经损伤。其范围从周围和眼部缺损到中枢和认知障碍。SCD患者应尽早进行定期神经学评估并调整危险因素,尤其要积极促进戒烟。