RESUMO
BACKGROUND: Blast-explosion may cause traumatic brain injury (TBI), leading to post-concussion syndrome (PCS). In studies on military personnel, PCS symptoms are highly similar to those occurring in post-traumatic stress disorder (PTSD), questioning the overlap between these syndromes. In the current study we assessed PCS and PTSD in civilians following exposure to rocket attacks. We hypothesized that PCS symptomatology and brain connectivity will be associated with the objective physical exposure, while PTSD symptomatology will be associated with the subjective mental experience. METHODS: Two hundred eighty nine residents of explosion sites have participated in the current study. Participants completed self-report of PCS and PTSD. The association between objective and subjective factors of blast and clinical outcomes was assessed using multivariate analysis. White-matter (WM) alterations and cognitive abilities were assessed in a sub-group of participants (n = 46) and non-exposed controls (n = 16). Non-parametric analysis was used to compare connectivity and cognition between the groups. RESULTS: Blast-exposed individuals reported higher PTSD and PCS symptomatology. Among exposed individuals, those who were directly exposed to blast, reported higher levels of subjective feeling of danger and presented WM hypoconnectivity. Cognitive abilities did not differ between groups. Several risk factors for the development of PCS and PTSD were identified. CONCLUSIONS: Civilians exposed to blast present higher PCS/PTSD symptomatology as well as WM hypoconnectivity. Although symptoms are sub-clinical, they might lead to the future development of a full-blown syndrome and should be considered carefully. The similarities between PCS and PTSD suggest that despite the different etiology, namely, the physical trauma in PCS and the emotional trauma in PTSD, these are not distinct syndromes, but rather represent a combined biopsychological disorder with a wide spectrum of behavioral, emotional, cognitive and neurological symptoms.
Assuntos
Lesões Encefálicas Traumáticas , Neurologia , Transtornos de Estresse Pós-Traumáticos , Humanos , Explosões , Síndrome , Transtornos de Estresse Pós-Traumáticos/etiologia , Lesões Encefálicas Traumáticas/complicaçõesRESUMO
BACKGROUND: The association between migraine and obesity gives the clinician with an exciting possibility to alleviate migraine suffering through weight-reduction gastric-restrictive operations. We hypothesized that bariatric weight-reduction intervention (gastric banding) will be associated with reduction of migraine burden in this population. METHODS: A total of 105 women between 18 and 50 years of age, admitted for bariatric surgery between April 2006 and February 2007, were screened for migraine. Twenty-nine with diagnosis of migraine were enrolled into the prospective phase. We followed the migraine pattern of these patients for 6 months post bariatric surgery. RESULTS: Baseline median migraine frequency was six headache days a month. Post bariatric surgery, the migraine-suffering women reported of a lower frequency of migraine attacks (p < 0.001), shorter duration of the attacks (p = 0.02), lower medication use during the attack (p = 0.005), less non-migraine pain (44.8 vs. 33%, p = 0.05), and post-bariatric surgery reduction in headache-related disability assessed by the MIDAS and HIT-6 scores. There was a reduction in migraine frequency among both episodic (from four to one episodes a month) and chronic (from 16.8 to 8.5 episodes per month) migraine patient cohorts separately and combined. CONCLUSIONS: Among migraine-suffering premenopausal obese women, we found a reduced frequency of migraine attacks and improvement of headache-related disability post bariatric surgery. Our findings should be interpreted cautiously. The absence of a control group and the non-blinded nature of our small study make it difficult to draw firm conclusions about the causal nature of the headache changes observed in this population. Further study is needed to evaluate the possible specific effects of surgical weight loss on migraine in obese women.
Assuntos
Cirurgia Bariátrica , Transtornos de Enxaqueca/epidemiologia , Obesidade Mórbida/complicações , Adolescente , Adulto , Feminino , Seguimentos , Humanos , Entrevistas como Assunto , Pessoa de Meia-Idade , Transtornos de Enxaqueca/complicações , Obesidade Mórbida/cirurgia , Pré-Menopausa , Estudos Prospectivos , Qualidade de Vida , Recidiva , Índice de Gravidade de Doença , Inquéritos e Questionários , Resultado do Tratamento , Redução de Peso , Adulto JovemRESUMO
Emery-Dreifuss muscular dystrophy (EDMD) is an X-linked humero-peroneal muscular dystrophy associated with contractures and cardiomyopathy. In a 90 member family, we found 11 affected male individuals, three of whom displayed areflexia and neurogenic electromyographic changes. Muscle biopsy performed in one case demonstrated type grouping suggestive of a neurogenic disorder. These three individuals and another family member, who suffers from mild, static limb weakness but is clinically and genetically unaffected by EDMD showed an abnormal incremental response of over 100% to tetanic stimulation. In contrast, one affected family member showed myopathic features on needle electromyography and no definite pathology in repetitive stimulation studies. The diagnosis of EDMD was established by demonstrating a 1712_1713insTGGGC mutation in the emerin gene. This family apparently expresses co-morbidity of EDMD with an exceptionally mild form of pre-synaptic congenital myasthenic syndrome resembling the Lambert-Eaton myasthenic syndrome (LEMS). The superimposed pre-synaptic disorder may have contributed to the development of the neurogenic features demonstrated in these patients.
Assuntos
Predisposição Genética para Doença/genética , Músculo Esquelético/fisiopatologia , Distrofia Muscular de Emery-Dreifuss/etnologia , Distrofia Muscular de Emery-Dreifuss/fisiopatologia , Síndromes Miastênicas Congênitas/etnologia , Síndromes Miastênicas Congênitas/fisiopatologia , Adolescente , Adulto , Árabes/genética , Criança , Pré-Escolar , Comorbidade , Análise Mutacional de DNA , Progressão da Doença , Feminino , Doenças Genéticas Ligadas ao Cromossomo X/etnologia , Doenças Genéticas Ligadas ao Cromossomo X/genética , Doenças Genéticas Ligadas ao Cromossomo X/fisiopatologia , Ligação Genética/genética , Testes Genéticos , Genótipo , Humanos , Masculino , Proteínas de Membrana/genética , Pessoa de Meia-Idade , Músculo Esquelético/inervação , Músculo Esquelético/patologia , Distrofia Muscular de Emery-Dreifuss/genética , Síndromes Miastênicas Congênitas/genética , Proteínas Nucleares/genética , Linhagem , FenótipoRESUMO
Pharmacotherapeutic intervention during traumatic memory consolidation has been suggested to alleviate or even prevent the development of posttraumatic stress disorder (PTSD). We recently reported that, in a controlled, prospective animal model, depriving rats of sleep following stress exposure prevents the development of a PTSD-like phenotype. Here, we report that administering the wake-promoting drug modafinil to rats in the aftermath of a stressogenic experience has a similar prophylactic effect, as it significantly reduces the prevalence of PTSD-like phenotype. Moreover, we show that the therapeutic value of modafinil appears to stem from its ability to stimulate a specific circuit within the hypothalamus, which ties together the neuropeptide Y, the orexin system and the HPA axis, to promote adaptive stress responses. The study not only confirms the value of sleep prevention and identifies the mechanism of action of a potential prophylactic treatment after traumatic exposure, but also contributes to understanding mechanisms underlying the shift towards adaptive behavioral response.
Assuntos
Adaptação Psicológica/efeitos dos fármacos , Compostos Benzidrílicos/farmacologia , Modelos Animais de Doenças , Hipotálamo/efeitos dos fármacos , Rede Nervosa/efeitos dos fármacos , Transtornos de Estresse Pós-Traumáticos/prevenção & controle , Transtornos de Estresse Pós-Traumáticos/psicologia , Vigília/efeitos dos fármacos , Animais , Nível de Alerta/efeitos dos fármacos , Nível de Alerta/fisiologia , Corticosterona/sangue , Humanos , Sistema Hipotálamo-Hipofisário/efeitos dos fármacos , Sistema Hipotálamo-Hipofisário/fisiopatologia , Masculino , Rememoração Mental/efeitos dos fármacos , Rememoração Mental/fisiologia , Modafinila , Neuropeptídeo Y/fisiologia , Orexinas/fisiologia , Sistema Hipófise-Suprarrenal/efeitos dos fármacos , Sistema Hipófise-Suprarrenal/fisiopatologia , Ratos , Ratos Sprague-DawleyRESUMO
OBJECTIVE: To describe three patients suffering from transient hemichorea/hemiballismus associated with hyperglycemia, review previous reports and propose a possible pathophysiological explanation for this phenomenon. RESULTS: Our original cases and previously reported ones reveal a uniform syndrome: mostly female patients (F/M ratio of 11/2), 50-80 years old, usually with no previous history of diabetes mellitus (9/13), develop choreic or ballistic movements on one side of the body over a period of hours. Serum glucose levels are elevated. In most of the patients, a lowering of the blood sugar level reverses the movement disorder within 24-48 hours. CONCLUSIONS: We believe that the combination of a recent or old striatal lesion (causing increased inhibition of the subthalamic nucleus) and hyperglycemia (causing decreased GABAergic inhibition of the thalamus) may be responsible for the appearance of this unilateral hyperkinetic movement disorder. Undiagnosed diabetes mellitus should always be suspected in patients who develop hemiballistic or hemichoreic movements. When hyperglycemia is detected and corrected, the movement disorder usually resolves within two days and may not require symptomatic therapy with dopamine receptor antagonists.
Assuntos
Coreia/diagnóstico , Discinesias/diagnóstico , Hiperglicemia/diagnóstico , Idoso , Gânglios da Base/patologia , Coreia/complicações , Coreia/fisiopatologia , Discinesias/complicações , Discinesias/fisiopatologia , Feminino , Lateralidade Funcional , Humanos , Hiperglicemia/complicações , Hiperglicemia/fisiopatologia , Pessoa de Meia-IdadeAssuntos
Anticonvulsivantes/efeitos adversos , Encefalite/induzido quimicamente , Insuficiência Renal/complicações , Ácido gama-Aminobutírico/análogos & derivados , Doença Aguda , Adulto , Idoso , Eletroencefalografia , Encefalite/complicações , Encefalite/diagnóstico , Epilepsia Generalizada/complicações , Epilepsia Generalizada/tratamento farmacológico , Humanos , Masculino , Vigabatrina , Ácido gama-Aminobutírico/efeitos adversosAssuntos
Autoanticorpos/sangue , Gangliosídeos/imunologia , Síndrome de Guillain-Barré/imunologia , Junção Neuromuscular/imunologia , Terminações Pré-Sinápticas/imunologia , Feminino , Síndrome de Guillain-Barré/fisiopatologia , Humanos , Síndrome Miastênica de Lambert-Eaton/fisiopatologia , Pessoa de Meia-Idade , Junção Neuromuscular/fisiopatologiaRESUMO
Fibromyalgia syndrome (FMS) is a chronic pain syndrome of unknown aetiology characterized by diffuse pain over more than 3 months and tenderness in specific sites named tender points. The aim of this study was to assess the prevalence and severity of FMS among patients suffering from episodic migraine. Ninety-two consecutive patients (20 male, 72 female) fulfilling the International Headache Society criteria for migraine with and without aura from a tertiary headache clinic were evaluated. A headache and generalized pain history was recorded, tender points were evaluated by thumb palpation. The diagnosis of FMS was made based on the 1990 American College of Rheumatology classification criteria for FMS. Sixteen (22.2%) of the female patients and none of the male patients were diagnosed as suffering from FMS. Migraine severity and characteristics were similar to other female migraine patients. Patients suffering from migraine-FMS had lower quality of life scores and higher levels of mental distress. A high incidence of FMS was found among female migraine patients but not in males. The coexistence of FMS should be considered when choosing a prophylactic migraine therapy.
Assuntos
Fibromialgia/diagnóstico , Fibromialgia/epidemiologia , Transtornos de Enxaqueca/diagnóstico , Transtornos de Enxaqueca/epidemiologia , Medição de Risco/métodos , Adulto , Idoso , Comorbidade , Avaliação da Deficiência , Escolaridade , Emprego , Feminino , Humanos , Israel/epidemiologia , Masculino , Estado Civil , Pessoa de Meia-Idade , Prevalência , Fatores de Risco , Índice de Gravidade de Doença , Distribuição por SexoRESUMO
A transient focal neurologic deficit after epileptic event is a well-known phenomenon. We report for the first time in English literature, three cases of transient urinary retention after seizures. The possible pathophysiologic mechanisms are discussed.
Assuntos
Convulsões/complicações , Convulsões/fisiopatologia , Retenção Urinária/complicações , Retenção Urinária/fisiopatologia , Adulto , Humanos , Masculino , Pessoa de Meia-IdadeRESUMO
Wernicke's encephalopathy (WE) is most commonly associated with alcoholism, although other causes have also been implicated. In the years 1994-1997, 9 patients with no history of alcohol abuse presented with acute signs of ophthalmoplegia or nystagmus and ataxia which resolved within 48 h after intravenous thiamine. There were 7 women and 2 men aged 17-57 (7 below the age of 30). Precipitating events included vomiting 2, drastic weight-reducing diet 2, renal colic in a postpartum woman 1, colonic surgery 2 and chronic hemodialysis 1. In 2 patients there was no obvious precipitating event but their history was suggestive of a genetic predisposition. Mental changes were slight or absent in all patients and all of them made good functional recovery. These cases suggest that the diagnosis of WE should be considered more often in nonalcoholics in various clinical settings.