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Dive into the research topics where Blagovest Nikolov is active.

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Featured researches published by Blagovest Nikolov.


Epilepsy & Behavior | 2000

A Pilot Study of Mood in Epilepsy Patients Treated with Vagus Nerve Stimulation

Cynthia L. Harden; Melissa C. Pulver; Lisa D. Ravdin; Blagovest Nikolov; James P. Halper; Douglas Labar

Context. Antiepileptic drugs (AEDs) are frequently used for their beneficial mood effects.Objective. We sought to determine if there was a quantifiable effect on mood of the vagus nerve stimulator (VNS) when used as an antiseizure treatment.Design. Mood was assessed before and 3 months after VNS implantation in adult epilepsy patients. A group of adult epilepsy patients on stable AED regimens were used as a comparison group. AED regimens were unchanged during the study. The change in mood scale scores across time was assessed by t test (intragroup) and two-factor repeated-measures ANOVA (intergroup).Setting. An epilepsy center in a university hospital was the setting.Subjects. Twenty consecutive adult epilepsy patients undergoing VNS implantation to improve seizure control and twenty adult seizure patients with no intervention were enrolled.Main outcome measures. The mood scales used were the Cornell Dysthymia Rating Scale (CDRS) and the Hamilton Depression (Ham-D), Hamilton Rating Scale for Anxiety (Ham-A), and Beck Depression Inventory (BDI) scales.Results. The VNS group showed a significant decrease in mood scale scores across time (t test CDRS P = 0.001, Ham-D P = 0.017, BDI P = 0.045), indicating a decrease in depressive symptoms. The Ham-A scores in the VNS group and the comparison group scores did not significantly change across time. There were no significant differences between groups across time, although the BDI approached significance at P = 0.07. The VNS group had a significant decrease in seizure frequency compared with the comparison group (P = 0.01). There was no difference in mood scales over time between the VNS treatment responders (defined by >50% decrease in seizure frequency) and nonresponders, suggesting dissociation between seizure frequency reduction and mood change.Conclusion. VNS treatment is associated with mood improvement as measured by multiple scales, but differences in mood scale scores over time between the VNS and a comparison group were not found.


Neurology | 2003

Seizure frequency is associated with age at menopause in women with epilepsy

Cynthia L. Harden; Barbara S. Koppel; Andrew G. Herzog; Blagovest Nikolov; W. A. Hauser

Objective: To determine whether the age at menopause in women with epilepsy is associated with seizure frequency. Methods: Women with epilepsy ages 45 and older from urban epilepsy centers were surveyed by interview and chart review for reproductive and general health characteristics, as well as seizure history, including frequency and treatment. Women who were not menopausal (≥1 year since last menses) were excluded. Subjects were divided into low, high, and intermediate seizure frequency groups. Statistical analyses included a one-way analysis of variance along with post hoc analysis (Bonferroni approach) to calculate pairwise comparisons. Results: Sixty-eight subjects had a mean age at last menses (menopause) of 47.8 years (SD ± 4.1, range 37 to 59 years). The age at menopause was 49.9 years in the low seizure frequency group (n = 15), 47.7 years in the intermediate seizure frequency group (n = 25), and 46.7 in the high seizure frequency group (n = 28). The difference in age at menopause in the three groups spanned approximately 3 years (p = 0.042). There was a negative correlation between the age at menopause and seizure group based on estimated lifetime seizures (p = 0.014, r = −0.310). No confounding influences such as history of cigarette smoking, number of pregnancies, or use of enzyme-inducing antiepileptic drugs were present. Conclusions: Seizure frequency or lifetime number of seizures is associated with the timing of cessation of reproductive cycling. Seizures may disrupt hypothalamic and pituitary function or alter neurally mediated trophic effects on the ovary.


Epilepsia | 2006

Hormone Replacement Therapy in Women with Epilepsy: A Randomized, Double-Blind, Placebo-Controlled Study

Cynthia L. Harden; Andrew G. Herzog; Blagovest Nikolov; Barbara S. Koppel; Paul J. Christos; Kristen M. Fowler; Douglas Labar; W. Allen Hauser

Summary:  Purpose: Previous reports have suggested that hormone replacement therapy (HRT) could increase seizure activity in women with epilepsy. We sought to determine whether adding HRT to the medication regimen of postmenopausal women with epilepsy was associated with an increase in seizure frequency.


Epilepsia | 1998

Vagus Nerve Stimulation for Symptomatic Generalized Epilepsy : A Pilot Study

Douglas Labar; Blagovest Nikolov; Brent Tarver; Richard A. R. Fraser

Summary: Purpose: Patients with symptomatic generalized epilepsy (SGE) may have antiepileptic drug (AED)‐resistant mixed generalized seizures. Vagus nerve stimulation (VNS) reduces partial seizures and may help SGE.


Epilepsy & Behavior | 2007

The effect of seizure severity on quality of life in epilepsy

Cynthia L. Harden; David Aaron Maroof; Blagovest Nikolov; Kristen M. Fowler; Michael R. Sperling; Joyce Liporace; Page B. Pennell; Douglas Labar; Andrew G. Herzog

Seizure severity is an important aspect of epilepsy. The relationship between seizure severity and quality of life in epilepsy, however, has been incompletely explored. With a data set of 118 women from the baseline phase of a clinical treatment trial, the relationship between seizure severity and aspects of quality of life was evaluated. Two domains of the Quality of Life in Epilepsy-31 (QOLIE-31) correlated highly significantly with seizure severity: Seizure Worry (r=-0.265, P=.004) and Social Functioning (r=-0.280, P=0.002). Two additional domains were significantly correlated: Overall Quality of Life (r=-0.210, P=0.023) and Cognitive (r=-0.209, P=0.024). When the potentially confounding effect of depression, measured by the Beck Depression Inventory, was controlled for, the regression of seizure severity with QOLIE-31 Seizure Worry remained significant (P=0.006, R(2)=0.153), as did the regression with QOLIE-31 Social Functioning (P=0.002, R(2)=0.184) and the regression with QOLIE-31 Cognitive (P=0.037, R(2)=0.30). These findings indicate that severe and potentially injurious seizure behaviors contribute to anxiety and socially avoidant behavior for persons with intractable epilepsy.


Epilepsia | 1999

A beneficial effect on mood in partial epilepsy patients treated with gabapentin.

Cynthia L. Harden; Lorraine M. Lazar; Lawrence H. Pick; Blagovest Nikolov; Martin Goldstein; Deborah Carson; Lisa D. Ravdin; James H. Kocsis; Douglas Labar

Summary: Purpose: Antiepileptic drugs (AEDs) are frequently used for their beneficial psychoactive effects on affective disorders. We sought to demonstrate a psychoactive effect of gabapentin (GBP) when used as add‐on AED therapy.


Epilepsia | 2004

Reaction to epilepsy in the workplace.

Cynthia L. Harden; Amy Kossoy; Susanne Vera; Blagovest Nikolov

Summary:  Purpose: The purpose of this study was to determine the characteristics of epilepsy that produce avoidant behavior in the workplace and therefore contribute to the actual stigma that persons with epilepsy are subjected to on the job.


Epilepsy & Behavior | 2009

A comparison of personality disorder characteristics of patients with nonepileptic psychogenic pseudoseizures with those of patients with epilepsy

Cynthia L. Harden; Luydmilla Jovine; Fadime T. Burgut; Bridget Carey; Blagovest Nikolov; Stephen J. Ferrando

We sought to determine the type of personality disorder cluster associated with patients with nonepileptic psychogenic seizures (NES) compared with that of patients with epileptic seizures (ES). Consecutive adult patients admitted for video/EEG monitoring found to have NES were compared with a simultaneously admitted patient with confirmed epilepsy. Personality was assessed using the Structured Clinical Interview for DSM-IV-TR Axis II Personality Disorders. Personality disorders were then divided into personality clusters described in the DSM-IV-TR: A = paranoid, schizotypal, schizoid; B = borderline, histrionic, antisocial, narcissistic; or C = avoidant, dependent, obsessive-compulsive. Thirteen of 16 patients with NES and 12 of 16 patients with ES met criteria for personality disorders. Patients with NES were more likely to meet criteria for a personality disorder in Cluster A or B, compared with patients with ES, who were more likely to have Cluster C personality disorders (chi(2) test, P=0.007). We propose that the personality traits of patients with NES contribute to the development of nonepileptic psychogenic seizures. However, the large proportion of patients with ES with Cluster C personality disorders was unexpected, and further, for the patients with epilepsy, the direction of the association of their personality traits with the development of epilepsy is unknown.


Acta Neurologica Scandinavica | 2005

An analysis of lifetime fractures in women with epilepsy.

Barbara S. Koppel; Cynthia L. Harden; Blagovest Nikolov; Douglas Labar

Objective – To clarify the relationship between fractures and antiepileptic drug (AED) use.


Epilepsia | 2010

Effect of levetiracetam on testosterone levels in male patients.

Cynthia L. Harden; Blagovest Nikolov; Padmaja Kandula; Douglas Labar; Susan Pannullo

We sought to determine whether the testosterone increase found with levetiracetam exposure in animal studies also occurs in patients. Adult male patients were evaluated for reproductive hormone levels before and 1 month after levetiracetam therapy. Eight subjects met inclusion/exclusion criteria (mean age 46 years, range 29–75 years). Total testosterone prior to starting levetiracetam ranged from 206–787 ng/dl [mean 445, standard deviation (SD) 227]. The mean total testosterone after levetiracetam therapy increased to 592 ng/dl (range 216–981, SD 297), an increase of 16% (p = 0.036). The free testosterone increased from a mean of 64 pg/ml (range 36–115, SD 30) to a mean of 76 pg/ml (range 35–155, SD 44), an increase of 19% (p = 0.080). The magnitude of change in testosterone levels correlated with the initial testosterone level (p = 0.038, r = 0.734). These results suggest that levetiracetam increases testosterone levels and that an initial testosterone level may predict the magnitude of increase.

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Andrew G. Herzog

Beth Israel Deaconess Medical Center

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Kristen M. Fowler

Beth Israel Deaconess Medical Center

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David Aaron Maroof

Albert Einstein College of Medicine

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