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Featured researches published by Seçil Arıca.


Graefes Archive for Clinical and Experimental Ophthalmology | 2014

Relationship between mean platelet volume and retinopathy in patients with type 2 diabetes mellitus

Esra Ayhan Tuzcu; Seçil Arıca; Nilufer Ilhan; Mutlu Cihan Daglioglu; Mesut Coskun; Ozgur Ilhan; Ihsan Ustun

ObjectivesTo evaluate the effect of mean platelet volume (MPV) on diabetic retinopathy in patients with type 2 diabetes mellitus.Materials and methodsIn this study, ocular findings and MPV values were retrospectively reviewed in 192 patients with type 2 diabetes mellitus. The patients were classified into four groups according to ocular findings, as follows: group 1, diabetic patients without diabetic retinopathy (n = 70); group 2, diabetic patients with non-proliferative diabetic retinopathy (n = 64); group 3, diabetic patients with proliferative diabetic retinopathy (n = 58); and group 4, healthy controls (n = 100).ResultsA significant difference was found in MPV values between groups 2 and 4 (P = 0.001), between groups 3 and 4 (P = 0.001), and between groups 1 and 4 (P = 0.004). No significant difference was found in MPV values between groups 1 and 2 (P = 0.241) and between groups 2 and 3 (P = 0.460); whereas there was a statistically significant difference between groups 1 and 3 (P = 0.015). The three diabetic groups (groups 1, 2, and 3) were compared with each other. While there was a statistically significant difference between groups 1 and 3 (P = 0.015), there was no significance between groups 2 and 3 (P = 0.46), and between group 1 and 2 (P = 0.241). Logistic regression analysis found a 1.40-fold increase in the risk of retinopathy development (OR: 1.404; P = 0.002) and a 1.46-fold increase in the risk of proliferative diabetic retinopathy (OR: 1.466; P = 0.002) as the MPV value increased.ConclusionsIn diabetic patients, the risk of retinopathy development increases with higher MPV values.


Journal of Affective Disorders | 2012

Serum adiponectin and resistin levels in patients with obsessive compulsive disorder

Mustafa Ari; Oktay Hasan Ozturk; Yasin Bez; Seçil Arıca; Yesim Can; Dudu Erduran

We aimed to investigate the changes in serum adiponectin and resistin levels in patients with obsessive compulsive disorder and control groups. The serum adiponectin and resistin levels of 29 patients (16 females, 13 males) with obsessive compulsive disorder and weight, age and sex-matched 31 healthy controls (17 females, 14 males) were determined. Yale-Brown Obsessive Compulsive Scale (Y-BOCS) was applied to all groups. ELISA method was used to measure adiponectin and resistin levels. The mean adiponectin level was 11.92±2.04 ng/ml and resistin level was 13.23±2.78 ng/ml in obsessive compulsive disorder group, while it was 18.81±5.24 ng/ml and 8.17±2.53 ng/ml in control group. Changes in plasma adiponectin and resistin levels in obsessive compulsive disorder may have implications about possible cardiovascular and metabolic abnormalities seen in obsessive compulsive patients.


Human & Experimental Toxicology | 2013

N-Acetylcysteine prevents doxorubucine-induced cardiotoxicity in rats

Vefik Arica; I.H. Demir; Murat Tutanç; Fatmagul Basarslan; Seçil Arıca; Murat Karcioglu; H. Öztürk; Ahmet Nacar

This study is designed to observe the effects of N-acetylcysteine (NAC) on doxorubucine-induced cardiac toxicity in rats both histologically and biochemically. Totally 32 rats divided equally into four groups were studied. The first group received only 200 mg/kg NAC intraperitoneal (i.p.) once every 24 h for 5 days (group 1); the second group received 20 mg/kg doxorubucine (DOX) i.p. single dose plus NAC 200 mg/kg i.p. once every 24 h for 5 days (group 2); the third group received DOX 20 mg/kg DOX i.p. single dose (group 3) and the fourth group, which is also the control group, received saline (group 4). Following 24 h of the final dose, blood samples were drawn from a portal vein and heart tissue were obtained. Tissue thiobarbituric acid reactive substance (TBARS) and nitric oxide (NO) levels were highest in the DOX group. In the DOX-treated rats, serum TBARS, NO, aspartate transaminase, lactate dehydrogenase and creatine kinase levels were highest when compared with other groups. Except for serum superoxide dismutase levels, all other parameters differed significantly between the DOX plus NAC group and the DOX group. In the DOX plus NAC group, general architecture was preserved better than the DOX group and myofibril loss was minimal compared with the DOX group. NAC demonstrated, both biochemically and histologically, to be effective in the prevention of DOX-induced cardiotoxicity in rat models. Evaluation of NAC’s effect on DOX toxicity warrants further clinical trials on cancer patients.


Scandinavian Journal of Urology and Nephrology | 2013

Relationship between endothelial dysfunction and nocturia with benign prostatic hyperplasia

Mehmet Inci; Bahadir Sarli; Mursel Davarci; Fatih Rüştü Yalçinkaya; Murat Mehmet Rifaioglu; Ramazan Davran; Seçil Arıca; Sedat Motor; Onur DemirbaŞ

Abstract Objective. There are limited data on whether there is an association between nocturia, benign prostatic hyperplasia (BPH) and endothelial dysfunction. The aim of the present study was to evaluate whether there is an association between nocturia and endothelial dysfunction in patients with BPH. Material and methods. Forty-two men with a diagnosis of BPH and 42 age-matched controls were enrolled. All patients were assessed for frequency and duration of nocturia, and prostate volume, completed the International Prostate Symptom Score (IPSS) questionnaire, and underwent brachial flow-mediated dilatation (FMD) evaluation. Results. There was a negative correlation between FMD and frequency of nocturia (r = –0.879, p < 0.0001). Moreover, there was a negative correlation between duration of nocturia and FMD (r = –0.890, p < 0.0001). In addition, FMD was significantly decreased in the BPH group compared with the control group (6.0 ± 0.09 to 7.8 ± 0.10%) (p = 0.0001). Conclusion. In patients with BPH, nocturia is associated with endothelial dysfunction and may be an insidious risk factor for cardiovascular disease.


Toxicology and Industrial Health | 2015

A 5-year retrospective evaluation of snakebite cases in Hatay, Turkey.

Ali Karakuş; Cem Zeren; Murat Celik; Seçil Arıca; Raif Özden; Mehmet Duru; Veyis Taşın

Snakebites are relatively rare medical emergency cases that might lead to serious consequences. This study aims to evaluate snakebite cases in terms of medical follow-up, antivenom therapy and antivenom reactions. Medical records of patients admitted to emergency department between January 1, 2006 and December 31, 2010 were retrospectively investigated. Snakebite-related cases of a total of 125 patients were included in the scope of the study. Of the total 125 cases, 54.4% were male and 45.6% were female. Most of cases (n: 65, 52%) were aged over 30 years, while the mean age was 34.87 ± 19.29 years. Snakebite-related applications to the emergency department were mostly seen in June with 27 cases. Upon admitting, all patients were recorded to be conscious and showing good general conditions; however, they suffered from pain and edema at the site of bite. Of all, 25 patients only suffered from bite injury and ecchymosis due to snakebite. The site of bite was upper extremities in 66 patients (52.8%), whereas it was lower extremities in 58 (46.4%). Of all, antivenom was unnecessary in 25 (20%) patients, while four antivenoms were administered to each of the 23 (18.4%) patients. Furthermore, six (4.8%) patients needed nine antivenom administrations for each. Anaphylaxis (n: 2, 1.6%), compartment syndrome (n: 2, 1.6%) and serum sickness (n: 1, 0.8%) encountered in remaining cases. Of all, 86 (68.8%) patients were hospitalized in the emergency department, while 25 (20.0%) patients were followed up by observation in emergency service. Only one patient was treated and followed up in intensive care unit. Implementation of antivenom therapy is considered unnecessary for the treatment of all snakebite cases. Antivenom reactions and number of related cases might be reduced by continuous close monitoring, appropriate prophylaxis and controlled slow infusion administration of medications.


Human & Experimental Toxicology | 2013

The scintigraphic evaluation and genetic correlation of joint involvements in pediatric patients with familial Mediterranean fever.

F. Aydogan; Murat Tutanç; Vefik Arica; Seçil Arıca; R. Gunesacar

Purpose: We aimed to evaluate the articular involvements in pediatric patients with familial Mediterranean fever (FMF) with joint symptoms by bone scintigraphy and to correlate the involved joints with the gene mutations. Materials and methods: A total of 41 newly diagnosed patients in pediatric age group (28 girls and 13 boys; mean age 9.14 ± 2.91 years) with joint involvement symptoms were included in this study. Scintigraphic images were obtained at 5th min (blood pool or early phase) and starting at 3 h (late phase) after (after tracer injection) intravenous administration of technetium-99m (99mTc)-methylendiphosphonate (MDP). Genomic DNA was isolated from leukocytes using standard salting out procedure. The sequencing data were analyzed. Results: Of the 41 patients, arthritis was found in 21 (51.2%) patients. Of the 21 patients, there was single joint involvement in 15 (71.4%) patients and multiple joint involvement in six (28.6%) patients. The mean age of patients with joint involvement (8 ± 2.3 years) were considerably lower than the patients without joint involvement (10.35 ± 3.04 years), and this was statistically significant (p = 0.008). The most commonly involved joints were ankles and knees. Multiple joint involvements were most frequently observed in the M694V and M694I gene mutations (16.7%). Conclusions: We use and recommend the bone scintigraphy in patients with FMF to determine the presence and distribution of arthritis, since bone scintigraphy is inexpensive, noninvasive, easy-to-use, and also is more sensitive in the diagnosis and distribution of arthritis than conventional radiological methods and clinical examination.


Human & Experimental Toxicology | 2012

Brucellosis with very high ferritin levels: report of five cases:

Vefik Arica; I Şilfeler; Seçil Arıca; Murat Tutanç; Vicdan Koksaldi Motor; Melek Inci

Brucellosis is a zoonotic disease caused by a kind of Brucella bacteria, which commonly appears in humans and rarely causes mortality. In our study, five cases, who were diagnosed by evaluation of clinical findings and serological tests, they also had very high ferritin levels, were reported. Ages of the patients were 16, 12, 10, 16 and 8 years, respectively. Serum ferritin levels were 1200, 985, 886, 748 and 435 ng/ml, respectively. We observed that complaints of the patients reduced after the treatment and ferritin levels returned to its normal range. In the situations of extremely evaluated serum ferritin which is an acute-phase reactant, its levels are able to raise in brucellosis, without existing hemochromatosis and Still’s disease


Journal of Clinical and Experimental Investigations | 2011

Hatay ilinde 2008 yılı kanser vakaları sıklığı ve dağılımı

Seçil Arıca; Ersin Nazlıcan; Cahit Özer; Dilek Benk Şilfeler; Vefik Arica; Tümay Özgür; Ümmahan Özaydın

Objective: The aim of this study was to evaluate all cancer cases reported in 2008 in Hatay district. Materials and methods: Data of 465 cancer patients were collected by Hatay Cancer Early Diagnosis and Screening Centre between January 1–December 31, 2008 and evaluated. Results: Totally 465 cancer cases were collected from centre of Hatay and districts. 48,8% of these cases (227 cases) were female patients, 51,2% (238 cases) were male. The most frequently encountered cancers were skin (27,7%) and breast cancers (14,7%) when evaluated in terms of the incidence of cases. Conclusion: Due to cancer screening studies becoming widespread in the community, cases with cancer can be determined in the early stage, also studies intended for etiology and preventive medicine gradually increase. Skin and breast cancers are common in Hatay. Therefore, further studies on etiology and preventive measures for cancer are needed. J Clin Exp Invest 2011;2(2):192-5


Clinical and Experimental Hypertension | 2012

Investigation of Parvovirus B19 Seroprevalence, Endothelin-1 Synthesis, and Nitric Oxide Levels in the Etiology of Essential Hypertension

Vicdan Koksaldi Motor; Seçil Arıca; Sedat Motor; Nigar Yilmaz; Ömer Evirgen; Melek Inci; Cumali Gokce; Yusuf Onlen

Background and Aims: Many studies have focused on the role of pathogen infection in hypertension (HT). It has been postulated that increased vascular tonus in HT is basically related to the imbalance between vasodilator, such as nitric oxide (NO), and vasoconstrictor, such as endothelin-1 (ET-1), substances secreted by endothelium. The aim of the present study was to investigate the seroprevalence of human parvovirus B19 (HPV B19) in the etiology of essential HT and the effect of HPV B19 on ET-1 and NO levels in this disorder. Materials and Methods: A total of 135 participants were enrolled in the study (90 patient and 45 controls). Antibodies to HPV B19 and ET-1 were measured by enzyme-linked immunosorbent assay method. Nitric oxide levels were calculated according to the Griess reaction. Results: Of the total participants, 27 patients (30%) and 7 control subjects (15.6%) had IgM positive (P = .068), whereas 27 patients (30%) and 14 control subjects (31.1%) had IgG positive (P = .895). There was no statistical difference between patients and control subjects in terms of serum ET-1 and NO levels. Conclusions: The role of HPV B19 in the etiology of essential HT was not shown in the present study. A larger sample may be needed for the investigation of these relations.


Human & Experimental Toxicology | 2011

Beta-ketothiolase deficiency brought with lethargy: Case report

Vefik Arica; Seçil Arıca; Hüseyin Dağ; Hatice Onur; Ömer Obut; Sayat Gülbayzar

Beta-ketothiolase deficiency is a rare autosomal recessive disorder of isoleucine and ketone body metabolism. This disorder is clinically characterized by ketoacidotic attacks. Ketoacidosis, vomiting, and dehydration, lethargy and coma may be seen during attacks. A 9-month-old girl was admitted to our hospital with acidosis and dehydration. The patient was lethargic. Ketoacidosis was suspected because of acetone odor on her breath. Her blood glucose level was 262 mg/dL and urine ketone was (++++). Branched chain amino acid levels were elevated in her blood sample. Organic acid analysis of urine revealed 2-methylacetoacetyl-CoA thiolase deficiency. This was reported because of rarity of the disease and we should consider it in the differential diagnosis of ketoacidotic episodes.

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Vefik Arica

Mustafa Kemal University

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Murat Tutanç

Mustafa Kemal University

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Cahit Özer

Mustafa Kemal University

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Ali Karakuş

Mustafa Kemal University

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Cem Zeren

Mustafa Kemal University

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Sedat Motor

Mustafa Kemal University

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Mesut Coskun

Mustafa Kemal University

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