Elif Uygur Kucukseymen

Dr. Elif Uygur Kucukseymen

orcid

Research Focus & Metrics

Academic Career Length

11Years (2016-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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30 October 2019 in BMJ Open
Verified
Journal Article
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LCLuis Castelo-Branco
Luis Castelo-Branco
EKElif Uygur Kucukseymen
Elif Uygur Kucukseymen
DDDante Duarte
Dante Duarte
MEMirret M El-Hagrassy
Mirret M El-Hagrassy
CPCamila Bonin Pinto
Camila Bonin Pinto
Felipe FregniFelipe Fregni
Felipe Fregni
Introduction Fibromyalgia (FM) is a common debilitating condition with limited therapeutic options. Medications have low efficacy and are often associated with adverse effects. Given that FM is associated with a defective endogenous pain control system and central sensitisation, combining interventions such as transcranial direct current stimulation (tDCS) and aerobic exercise (AE) to modulate pain-processing circuits may enhance pain control. Methods and analysis A prospective, randomised (1:1:1:1), placebo-controlled, double-blind, factorial clinical trial will test the hypothesis that optimised tDCS (16 anodal tDCS sessions combined with AE) can restore of the pain endogenous control system. Participants with FM (n=148) will undergo a conditioning exercise period and be randomly allocated to one of four groups: (1) active tDCS and AE, (2) sham tDCS and AE, (3) active tDCS and non-aerobic exercise (nAE) or (4) sham tDCS and nAE. Pain inhibitory activity will be assessed using conditioned pain modulation (CPM) and temporal slow pain summation (TSPS)—primary outcomes. Secondary outcomes will include the following assessments: Transcranial magnetic stimulation and electroencephalography as cortical markers of pain inhibitory control and thalamocortical circuits; secondary clinical outcomes on pain, FM, quality of life, sleep and depression. Finally, the relationship between the two main mechanistic targets in this study—CPM and TSPS—and changes in secondary clinical outcomes will be tested. The change in the primary efficacy endpoint, CPM and TSPS, from baseline to week 4 of stimulation will be tested with a mixed linear model and adjusted for important demographic variables. Ethics and dissemination This study obeys the Declaration of Helsinki and was approved by the Institutional Review Board (IRB) of Partners Healthcare under the protocol number 2017P002524. Informed consent will be obtained from participants. Study findings will be reported in conferences and peer-reviewed journal publications. Trial registration number NCT03371225.

4 August 2023 in Multiple Sclerosis and Related Disorders
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Journal Article
Closed access
EKElif Uygur Kucukseymen
Elif Uygur Kucukseymen
KPKevin Pacheco-Barrios
Kevin Pacheco-Barrios
BYBurcu Yuksel
Burcu Yuksel
PGPaola Gonzalez-Mego
Paola Gonzalez-Mego
ASAysun Soysal
Aysun Soysal
FFFelipe Fregni
Felipe Fregni

1 April 2022 in The Lancet Regional Health - Americas
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Journal Article
Open access
KPKevin Pacheco-Barrios
Kevin Pacheco-Barrios
ANAlba Navarro-Flores
Alba Navarro-Flores
ACAlejandra Cardenas-Rojas
Alejandra Cardenas-Rojas
PMPaulo S. de Melo
Paulo S. de Melo
EKElif Uygur Kucukseymen
Elif Uygur Kucukseymen
JBJorge G. Burneo
Jorge G. Burneo
Background The epilepsy prevalence in Latin America and the Caribbean (LAC) had remained high over the last 20 years. Data on the burden of epilepsy are needed for healthcare planning and resource allocation. However, no systematic analysis had been performed for epilepsy burden in LAC. Methods We extracted data of all LAC countries from the Global Burden of Disease (GBD) study from 1990 to 2019. Epilepsy burden was measured as prevalence, mortality, and disability-adjusted life-years (DALYs; defined by the sum of years of life lost [YLLs] for premature mortality and years lived with disability [YLDs]), by age, sex, year, and country. Absolute numbers, rates, and 95% uncertainty intervals were reported. We performed correlational analyses among burden metrics and Socio-demographic Index (SDI). Findings The burden of epilepsy decreased around 20% in LAC, led by YLLs reduction. In 2019, 6 center dot 3 million people were living with active epilepsy of all causes (95% UI 5 center dot 3 - 7 center dot 4), with 3 center dot 22 million (95% UI 2 center dot 21 - 4 center dot 03) and 3 center dot 11 million (95% UI 2 center dot 21 to 4 center dot 03) cases of epilepsy with identifiable aetiology and idiopathic epilepsy, respectively. The number of DALYs represented the 9 center dot 51% (1.37 million, 95% UI 0 center dot 99 -1 center dot 86) of the global epilepsy burden in 2019. The age-standardized burden was 175 center dot 9 per 100 000 population (95% UI 119 center dot 4 - 253 center dot 3), which tend to have a bimodal age distribution (higher in the youth and elderly) and was driven by high YLDs estimates. The burden was higher in men and older adults, primarily due to high YLLs and mortality. Alcohol use was associated with 17% of the reported DALYs. The SDI estimates significantly influenced this burden (countries with high SDI have less epilepsy burden and mortality, but not prevalence or disability). Interpretation The epilepsy burden has decreased in LAC over the past 30 years. Even though, LAC is still ranked as the third region with the highest global epilepsy burden. This reduction was higher in children, but burden and mortality increased for older adults. The epilepsy burden is disability predominant; however, the mortality-related estimates are still higher than in other regions. Alcohol consumption and countries' development are important determinants of this burden. There is an urgent need to improve access to epilepsy care in LAC, particularly for older adults. Strengthening primary care with online learning and telemedicine tools, and promoting risk factors modification should be prioritized in the region. Copyright (c) 2021 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/)

17 November 2021 in Contemporary Clinical Trials Communications
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Journal Article
Open access
ACAlejandra Cardenas-Rojas
Alejandra Cardenas-Rojas
LCLuis Castelo-Branco
Luis Castelo-Branco
KPKevin Pacheco-Barrios
Kevin Pacheco-Barrios
ESEmad Salman Shaikh
Emad Salman Shaikh
EKElif Uygur Kucukseymen
Elif Uygur Kucukseymen
Felipe FregniFelipe Fregni
Felipe Fregni
Fibromyalgia is a complex pain condition that affects mostly women. Given the disease's lack of understanding, patients report poor adherence to medication and mistrust of medical services. This study aims to describe the recruitment characteristics and non-adherence associated factors of fibromyalgia patients to an RCT. We performed a retrospective longitudinal analysis with data from our ongoing RCT. We investigated characteristics of subjects recruited, consented, and randomized. Adherence was studied using survival analysis techniques, and its associated factors were identified using Cox proportional hazards regression model. 524 subjects were contacted, 269 were eligible, 61 consented and 40 subjects were randomized. Thirty-eight percent were non-adherent to the protocol with a median of visits of five. The recruitment survey reported that 90% would likely participate in RCTs, 52% had previous participation, and 19% were aware of RCTs by their physicians. Some barriers were investigator-related (staff's friendliness and receiving the results of their trial participation) and center-related (privacy-confidentiality issues and the institution's reputation), without difference between adherent and non-adherent participants. We report significant factors for non-adherence as VAS anxiety score of 5 or more (5.3 HR, p = 0.01), Body Mass Index (BMI) (0.91 HR, p = 0.041) and Quality of Life (QoL) – Personal development subdomain (0.89 HR, p = 0.046). Recruitment and adherence of fibromyalgia patients is a challenge; however, they seem eager to participate in RCTs. We recommend creating a comfortable, friendly and trusting environment to increase the recruitment rate. Higher anxiety, lower BMI and lower quality of life were associated with a higher attrition rate.

4 September 2022 in Neurological Research
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Journal Article
Closed access
EKElif Uygur Kucukseymen
Elif Uygur Kucukseymen
GAGizem Akca
Gizem Akca
Migraine is one of the most prevalent and disabling conditions worldwide. Dyslipidemia has become an issue of great importance recently in migraine patients. There is still no consensus on the rela...

2 December 2018 in Expert Review of Medical Devices
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Journal Article
Closed access
DDDante Duarte
Dante Duarte
LCLuis Eduardo Coutinho Castelo-Branco
Luis Eduardo Coutinho Castelo-Branco
EKElif Uygur Kucukseymen
Elif Uygur Kucukseymen
Felipe FregniFelipe Fregni
Felipe Fregni
Introduction: Fibromyalgia affects more than 5 million people in the United States and has a detrimental impact on individuals’ quality of life. Current pharmacological treatments provide limited benefits to relieve the pain of fibromyalgia, along with a risk of adverse effects; a scenario that explains the increasing interest for multimodal approaches. A tailored strategy to focus on this dysfunctional endogenous pain inhibitory system is transcranial direct current stimulation (tDCS) of the primary motor cortex. By combining tDCS with aerobic exercise, the effects can be optimized. Areas covered: The relevant literature was reviewed and discussed the methodological issues for designing a mechanistic clinical trial to test this combined intervention. Also, we reviewed the neural control of different pathways that integrate the endogenous pain inhibitory system, as well as the effects of tDCS and aerobic exercise both alone and combined. In addition, potential neurophysiological assessments are addressed: conditioned pain modulation, temporal slow pain summation, transcranial magnetic stimulation, and electroencephalography in the context of fibromyalgia. Expert commentary: By understanding the neural mechanisms underlying pain processing and potential optimized interventions in fibromyalgia with higher accuracy, the field has an evident potential of advancement in the direction of new neuromarkers and tailored therapies.