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1.
Neurol Genet ; 10(5): e200188, 2024 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-39246739

RESUMEN

Background and Objectives: Amyotrophic lateral sclerosis (ALS) is an age-associated, fatal neurodegenerative disorder causing progressive paralysis and respiratory failure. The genetic architecture of ALS is still largely unknown. Methods: We performed a genome-wide association study (GWAS) and transcriptome-wide association study (TWAS) to understand genetic risk factors for ALS using a population-based case-control study of 435 ALS cases and 279 controls from Northern New England and Ohio. Single nucleotide polymorphism (SNP) genotyping was conducted using the Illumina NeuroChip array. Odds ratios were estimated using covariate-adjusted logistic regression. We also performed a genome-wide SNP-smoking interaction screening. TWAS analyses used PrediXcan to estimate associations between predicted gene expression levels across 15 tissues (13 brain tissues, skeletal muscle, and whole blood) and ALS risk. Results: GWAS analyses identified the p.A382T missense variant (rs367543041, p = 3.95E-6) in the TARDBP gene, which has previously been reported in association with increased ALS risk and was found to share a close affinity with the Sardinian haplotype. Both GWAS and TWAS analyses suggested that ZNF235 is associated with decreased ALS risk. Discussion: Our results support the need for future evaluation to clarify the role of these potential genetic risk factors for ALS and to understand genetic susceptibility to environmental risk factors.

2.
Neurotoxicology ; 87: 128-135, 2021 12.
Artículo en Inglés | MEDLINE | ID: mdl-34562505

RESUMEN

BACKGROUND: Environmental exposures are implicated in the etiology of amyotrophic lateral sclerosis (ALS). Application of insecticides, herbicides, and fungicides with neurotoxic properties to crops is permitted in the U.S., however reporting of the quantities is government mandated. OBJECTIVE: To identify pesticides that may be associated with ALS etiology for future study. METHODS: We geospatially estimated exposure to crop-applied pesticides as risk factors for ALS in a large de-identified medical claims database, the SYMPHONY Integrated Dataverse®. We extracted residence at diagnosis of ∼26,000 nationally distributed ALS patients, and matched non-ALS controls. We mapped county-level U.S. Geological Survey data on applications of 423 pesticides to estimate local residential exposure. We randomly broke the SYMPHONY dataset into two groups to form independent discovery and validation cohorts, then confirmed top hits using residential history information from a study of NH, VT, and OH. RESULTS: Pesticides with the largest positive statistically significant associations in both the discovery and the validation studies and evidence of neurotoxicity in the literature were the herbicides 2,4-D (OR 1.25 95 % CI 1.17-1.34) and glyphosate (OR 1.29 95 %CI 1.19-1.39), and the insecticides carbaryl (OR 1.32 95 %CI 1.23-1.42) and chlorpyrifos (OR 1.25 95 %CI 1.17-1.33). SIGNIFICANCE: Our geospatial analysis results support potential neurotoxic pesticide exposures as risk factors for sporadic ALS. Focused studies to assess these identified potential relationships are warranted.


Asunto(s)
Esclerosis Amiotrófica Lateral/inducido químicamente , Exposición a Riesgos Ambientales/efectos adversos , Plaguicidas/toxicidad , Ácido 2,4-Diclorofenoxiacético/toxicidad , Anciano , Anciano de 80 o más Años , Carbaril/toxicidad , Cloropirifos/toxicidad , Producción de Cultivos/métodos , Exposición a Riesgos Ambientales/estadística & datos numéricos , Femenino , Glicina/análogos & derivados , Glicina/toxicidad , Herbicidas/toxicidad , Humanos , Insecticidas/toxicidad , Masculino , Persona de Mediana Edad , Factores de Riesgo , Estados Unidos/epidemiología , Glifosato
3.
Neuroepidemiology ; 55(5): 416-424, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-34218222

RESUMEN

BACKGROUND: Amyotrophic lateral sclerosis (ALS) is a neurological disease of largely unknown etiology with no cure. The National ALS Registry is a voluntary online system that collects demographic and reproductive history (females only) data from patients with ALS. We will examine the association between demographic and reproductive history among female patients aged >18 years and various ages of onset for ALS. METHODS: Data from a cross-sectional study were collected and examined for 1,018 female ALS patients. Patient characteristics examined were demographics including race, BMI, and familial history of ALS. Among patients, information on reproductive history, including age at menopause, ever pregnant, and age at first pregnancy was collected. Unadjusted and adjusted logistic regression models were used to estimate OR and 95% CI in this study. RESULTS: Women were more likely to be diagnosed with ALS before age 60 if they were nonwhite (p = 0.015), had attended college (p = 0.0012), had a normal BMI at age 40 (p < 0.0001), completed menopause before age 50 (p < 0.0001), and had never been pregnant (p = 0.046) in the univariate analysis. Women diagnosed with ALS before age 60 were also more likely to have limb site of onset (p < 0.0001). In the multivariate analysis, those who completed menopause before age 50 were more likely to be diagnosed with ALS before age 60 (OR = 1.8, 95% CI: 1.4-2.3) compared with women who completed menopause at or after age 50, after controlling for race, ever pregnant, age at first pregnancy, family history of ALS, education status, smoking history, and BMI at age 40. For women who were diagnosed with ALS before age 50, the odds of them entering menopause before age 50 climb to 48.7 (95% CI: 11.8, 200.9). The mean age of ALS diagnosis for women who completed menopause before age 50 was 58 years and 64 years for women who entered menopause after age 50 (p < 0.0001). CONCLUSION: Women who reported completing menopause before age 50 were significantly more likely to be diagnosed with ALS before age 60 compared with those who reported entering menopause after age 50. More research is needed to determine the relationship between female reproductive history, especially regarding endogenous estrogen exposure and early-onset ALS.


Asunto(s)
Esclerosis Amiotrófica Lateral , Adulto , Edad de Inicio , Esclerosis Amiotrófica Lateral/epidemiología , Estudios Transversales , Femenino , Humanos , Persona de Mediana Edad , Embarazo , Sistema de Registros , Historia Reproductiva , Factores de Riesgo
4.
Spine (Phila Pa 1976) ; 35(13): E614-6, 2010 Jun 01.
Artículo en Inglés | MEDLINE | ID: mdl-20461029

RESUMEN

STUDY DESIGN: Case report and review of literature. OBJECTIVE: Review the common side-effects of interlaminar cervical epidural injection (CEI) and to report a novel complication of this procedure. SUMMARY OF BACKGROUND AND DATA: CEIs are commonly used to treat chronic radicular neck pain. Several minor and major complications have been reported in literature. We report a rare complication of syrinx formation resulting from a CEI. METHODS: A 52-year-old woman presented from an outside hospital after undergoing a CEI. Under fluoroscopic guidance, an epidural needle was inserted at C7-T1 level. Radiologic contrast showed appropriate epidural spread. Shortly after waking up from the procedure, the patient complained of inability to move her right arm and leg, numbness of her right hemibody below the neck, and urinary retention. RESULTS: Magnetic resonance imaging of the spine revealed a syrinx extending from the C1 to T4 levels. There was no evidence of epidural collection or blood. CONCLUSION: Interlaminar CEI is thought to be a relatively safe procedure. Spinal cord injury is a documented complication of spinal anesthesia at any level of the spinal cord, even with fluoroscopic guidance, but most complications are thought to be minor and transient in nature. Syrinx formation with focal myelomalacia following spinal anesthesia has been reported in the lumbar area Pradhan et al, J Neurol Sci 2006;251:70-2, but we know of no existing reports involving the cervical region. We report this rare complication in this case report.


Asunto(s)
Vértebras Cervicales , Siringomielia/diagnóstico , Siringomielia/fisiopatología , Femenino , Humanos , Inyecciones Epidurales/efectos adversos , Persona de Mediana Edad , Siringomielia/etiología
5.
Amyotroph Lateral Scler ; 10(5-6): 476-8, 2009.
Artículo en Inglés | MEDLINE | ID: mdl-19922143

RESUMEN

We report a 54-year-old male with progressive and asymmetrical lower extremity weakness caused by familial amyotrophic lateral sclerosis (FALS) with a Cu/Zn superoxidase dismutase 1 (SOD1) gene mutation. He was initially misdiagnosed with a lumbosacral polyradiculopathy because of spinal stenosis and underwent a laminectomy surgery with no benefit. He was also misdiagnosed with a myopathy due to moderate CK elevation from acute denervation and pseudomyopathic changes on muscle biopsies from chronic denervation. He eventually developed respiratory muscle weakness and upper motor neuron signs, consistent with familial ALS.


Asunto(s)
Esclerosis Amiotrófica Lateral/diagnóstico , Esclerosis Amiotrófica Lateral/genética , Enfermedades Musculares/diagnóstico , Mutación , Polirradiculopatía/diagnóstico , Superóxido Dismutasa/genética , Esclerosis Amiotrófica Lateral/enzimología , Esclerosis Amiotrófica Lateral/patología , Diagnóstico Diferencial , Errores Diagnósticos , Humanos , Masculino , Persona de Mediana Edad , Músculo Esquelético/patología , Enfermedades Musculares/genética , Enfermedades Musculares/patología , Polirradiculopatía/genética , Polirradiculopatía/patología , Superóxido Dismutasa-1
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