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The effect of monthly mean global horizontal solar radiation and sunshine duration on vitamin d levels in young women 月平均全球水平太阳辐射和日照时间对年轻女性维生素d水平的影响
Pub Date : 2023-10-29 DOI: 10.30565/medalanya.1274708
Şükriye TAŞÇI KARAGÖL, Sevil TURHAN, Hülya COŞKUN, Seher KIR, Yusuf Emre. BOSTAN, Raziye YILDIZ
Aim: The most important reason for vitamin D deficiency is the lack of synthesis in the skin. The synthesis of vitamin D can be affected by many variables such as geographical region, race, season, monthly average daily sun exposure (MADSD), monthly average daily global horizontal solar radiation (MADGHSR). In this study, we aimed to investigate possible association between vitamin D levels and MADSD and MADGHSR in young women. Methods: This is a retrospective study evaluating the levels of Vitamin D classified by age, seasons, months, MADGHSR and MADSD in women aged between 15-45 years admitted to a secondary state hospital. Results: All of the women involved were at reproductive age and approximately 94.6% of them had vitamin D levels below 30 ng/mL. The median (minimum-maximum) vitamin D level was 16.1 (3.6-49.4) ng/mL in summer and 14.3 (3.2-49.8) ng/mL in winter (p=0.001). The rate of vitamin D deficiency (<20 ng/mL) was 68.1% in summer and 75.1% in winter (p<0.001). The median MADGHSR was 4.6 (3.4-5.7) hours in winter and 6.9 (5.2-7.2) hours in summer and the median MADSD was 3.3 (1.6-3.5) watt/m²/day in winter and 15.2 (12.2-15.8) watt/m²/day in summer. Vitamin D level was weakly correlated with age (r=0.082, p=0.002), MADSD (r=0.075, p=0.001) and MADGHSR (r=0.062, p=0.006). Conclusion: We found that MADGHSR and MADSD had an effect on vitamin D synthesis in addition to factors related with personal and environmental situations. We suggest that routine optimal dose vitamin D replacement is necessary in geographies similar to the population in our study.
目的:维生素D缺乏的最重要原因是皮肤缺乏合成。维生素D的合成受地理区域、种族、季节、月平均日晒量(MADSD)、月平均日全球水平太阳辐射(MADGHSR)等多种因素的影响。在这项研究中,我们旨在探讨维生素D水平与年轻女性MADSD和MADGHSR之间的可能关联。方法:这是一项回顾性研究,以年龄、季节、月份、MADGHSR和MADSD分类评估一家二级公立医院收治的15-45岁妇女的维生素D水平。结果:所有参与研究的女性都处于生育年龄,其中约94.6%的女性维生素D水平低于30 ng/mL。夏季维生素D水平中位数(最小-最大)为16.1 (3.6-49.4)ng/mL,冬季为14.3 (3.2-49.8)ng/mL (p=0.001)。维生素D缺乏率(20 ng/mL)夏季为68.1%,冬季为75.1% (p amp;lt;0.001)。MADGHSR中位数冬季为4.6(3.4-5.7)小时,夏季为6.9(5.2-7.2)小时,MADSD中位数冬季为3.3(1.6-3.5)瓦特/平方米/天,夏季为15.2(12.2-15.8)瓦特/平方米/天。维生素D水平与年龄(r=0.082, p=0.002)、MADSD (r=0.075, p=0.001)、MADGHSR (r=0.062, p=0.006)呈弱相关。结论:我们发现除了个人和环境因素外,MADGHSR和MADSD对维生素D合成也有影响。我们建议,在与我们研究的人群相似的地区,常规的最佳剂量维生素D替代是必要的。
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引用次数: 0
Apoptosis Induction Through Increased TRPV1 Activation by Synergic Effect of Melatonin and Doxorubicin in Human Osteosarcoma and Chondrosarcoma Cell Lines 褪黑素和阿霉素协同作用下增加TRPV1激活诱导人骨肉瘤和软骨肉瘤细胞系细胞凋亡
Pub Date : 2023-10-29 DOI: 10.30565/medalanya.1313745
Ahmet KOÇAK, Anıl GÜLCÜ, İshak Suat ÖVEY
Aim: We aimed to reveal the role of doxorubicin (Dox), melatonin (Mel) and transient receptor potential Vanilloid 1 (TRPV1) channels in bone and cartilage cancer cells during the treatment process. Human Bone Osteosarcoma (Saos-2/An1) and Human Chondrosarcoma (Hs 819.T) cell lines were used to prepare in-vitro experiment models. Methods: Both cell lines were cultured at 37°C. We have separated each cell line into five groups as follows: Controls, Dox, Dox+Capsazepine (Cpz), Dox+Melatonin (Mel), and combined Dox+Mel+Cpz given group. Capsaicin and capsazepine were added to cell culture mediums to activate or inactivate the TRPV1 channels, respectively. Cytosolic calcium, apoptosis, intracellular reactive oxygen, mitochondrial depolarization, caspase-3 and caspase-9 levels were measured. Results: Increased apoptotic activity was detected in doxorubicin given cell lines (Group II) when compared with the controls (p˂0.001). There was also a significantly higher apoptotic level in Dox+Mel group (Group IV), when compared with only Dox given group (p˂0.001). TRPV1 inhibition applied groups (Group III and V) have had lower apoptotic levels than other drug administered groups (p˂0.001). Conclusion: This study has indicated that apoptotic effects of Dox and Mel on both osteosarcoma and chondrosarcoma were strictly associated to TRPV1 channels, and that TRPV1 channels played an important role in whole mitochondria dependent pathways of apoptosis, which in turn may lead to increased intracellular Ca+2 levels and mitochondrial depolarization.
目的:揭示多柔比星(Dox)、褪黑素(Mel)和瞬时受体电位Vanilloid 1 (TRPV1)通道在骨和软骨癌细胞治疗过程中的作用。采用人骨骨肉瘤(Saos-2/An1)和人软骨肉瘤(Hs 819.T)细胞系制备体外实验模型。方法:两种细胞系均在37℃培养。我们将每个细胞系分为五组:对照组,Dox, Dox+Capsazepine (Cpz), Dox+褪黑素(Mel)和Dox+Mel+Cpz联合给药组。在细胞培养基中加入辣椒素和辣椒平,分别激活或灭活TRPV1通道。测定细胞质钙、细胞凋亡、细胞内活性氧、线粒体去极化、caspase-3和caspase-9水平。结果:与对照组相比,给予阿霉素的细胞系(II组)的凋亡活性增加(p小于0.001)。与只给Dox组相比,Dox+Mel组(IV组)的细胞凋亡水平也显著升高(p小于0.001)。TRPV1抑制组(III组和V组)的细胞凋亡水平低于其他给药组(p小于0.001)。结论:本研究提示Dox和Mel对骨肉瘤和软骨肉瘤的凋亡作用均与TRPV1通道密切相关,TRPV1通道在整个线粒体依赖的凋亡通路中发挥重要作用,进而可能导致细胞内Ca+2水平升高和线粒体去极化。
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引用次数: 0
Determination of Bone Developments of Rat Anterior and Posterior Extremity Bones in Prenatal and Postnatal Period by Double Staining Method 双染色法测定大鼠产前、产后前后肢体骨发育
Pub Date : 2023-10-29 DOI: 10.30565/medalanya.1262518
Mustafa ÖZTÜRK, Erdoğan UNUR, Niyazi ACER, Tolga ERTEKİN, Serife ALPA, Mesut MEKER, Yahya TAHTA
Aim: In our study, we aimed to determine the morphological development of the bones of the anterior and posterior extremity by staining the rat fetus and offspring skeletons with the double staining method. Method: In the current study, seven groups three prenatal (16th, 18th, and 20th days) and four postnatal (0th, 3th, 7th and 12th days) were formed from the foetuses and offsprings obtained from 13 pregnant rats. Then, it was stained with double staining method. Anterior and posterior extremity images of the fetuses and offsprings were examined under a stereo microscope, and ossification findings were determined. Total bone and ossification lengths as well as ossification areas were measured using the ImageJ software. Results: The first cartilage destruction in fetuses occurred on the 16th day of pregnancy in the clavicle, scapula, humerus, radius and ulna; It was seen in the femur, tibia and fibula on the 18th day of pregnancy. The first ossification centres were in the clavicle, scapula and humerus on the 18th day of pregnancy; It was seen in the radius, ulna, femur, tibia, fibula and 2-5 metatarsal bones on the 20th day of pregnancy. The secondary ossification centre was seen on the 0th day (birthday) in the scapula and humerus, on the 7th day after birth in the ulna and radius, and on the 12th day after birth in the femur and tibia. In the study, while the ossification rate in 20-day-old foetuses was 48.9% in the humerus, 53.2% in the radius, 55.7% in the ulna, 33.6% in the femur, 43.2% in the tibia, 44.3% in the fibula, it was determined that it reached 69.7% in the humerus, 78.4% in the radius, 73.3% in the ulna, 63.5% in the femur, 75.5% in the tibia, and 69.2% in the fibula on the 12th day after birth. Conclusion: In this study, we revealed the morphological changes of the anterior and posterior extremity bones of fetuses and offsprings in the normal developmental course. We think that these results will shed light on the studies to be conducted on the detection of skeletal anomalies in teratological studies and contribute to a more comprehensive evaluation of the findings to be obtained from the studies to be conducted.
目的:采用双染色法对大鼠胎儿和子代骨骼进行染色,观察其前后肢体骨骼的形态发育情况。方法:选取13只妊娠大鼠的胎仔共7组,分别为产前(第16、18、20天)和产后(第0、3、7、12天)。然后用双染色法进行染色。在立体显微镜下检查胎儿和后代的前肢和后肢图像,并确定骨化结果。使用ImageJ软件测量总骨和骨化长度以及骨化面积。结果:胎儿第一次软骨破坏发生在妊娠第16天的锁骨、肩胛骨、肱骨、桡骨和尺骨;妊娠第18天在股骨、胫骨和腓骨可见。妊娠第18天,第一批骨化中心在锁骨、肩胛骨和肱骨;妊娠第20天桡骨、尺骨、股骨、胫骨、腓骨及2 ~ 5跖骨可见。出生后第0天(生日)肩胛骨和肱骨出现继发性骨化中心,出生后第7天尺骨和桡骨出现继发性骨化中心,出生后第12天股骨和胫骨出现继发性骨化中心。本研究中,20日龄胎儿骨化率肱骨为48.9%,桡骨为53.2%,尺骨为55.7%,股骨为33.6%,胫骨为43.2%,腓骨为44.3%,确定在出生后第12天,肱骨骨化率为69.7%,桡骨为78.4%,尺骨为73.3%,股骨为63.5%,胫骨为75.5%,腓骨为69.2%。结论:本研究揭示了胎儿和子代在正常发育过程中四肢前后骨的形态学变化。我们认为,这些结果将有助于对畸形学研究中骨骼异常检测的研究进行阐明,并有助于对即将进行的研究结果进行更全面的评估。
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引用次数: 0
Uzak metastazlı kanser hastalarında iskelet kası kütlesinin prediktif ve prognostik değeri 癌症远处转移患者骨骼肌质量的预测和预后价值
Pub Date : 2023-10-29 DOI: 10.30565/medalanya.1167930
Tülay KUŞ, Mahmut ÇORAPLI, Baran YUSUFOĞLU, Gökmen AKTAŞ, Cemil OKTAY
Aim:Skeletal muscle loss is an indicator of cachexia and a strong prognostic factor for some types of cancer. After strict standardization, we aim to evaluate both the predictive and prognostic value of low muscle mass (LMM) in common cancer types for first-line chemotherapy. Methods: This retrospective single-center study was conducted in a regional hospital between 2015 and 2020. Patients diagnosed with distant metastatic cancer were screened and included in the study if they had abdominal computed tomography 45 days prior to first-line chemotherapy. The relationship between LMM and progression-free survival (PFS), overall survival (OS), and objective response rate (ORR) was evaluated. Results: Initially, 289 patients with metastatic cancer were included. The median duration of follow-up was 17 months, with a mean age of 61.09±13.03 years (range 25 to 95), and 45.9% of patients were female. In total, 50.5% of patients had LMM, which was adjusted for gender. LMM was associated with worse OS and PFS in univariate analysis (HR:1.598;1.216-2.100; p=0.001 for OS and HR:1.583;1.216-2.059; p=0.001 for PFS), and this positive association was maintained after adjusted for diagnosis and age. Better ORRs were obtained in respiratory and gastrointestinal tract cancers, breast, prostate and gynecological cancer in non-LMM groups. Conclusion:LMM has not only prognostic value but also predictive value for many types of cancer. Therefore, the assessment of muscle loss should be incorporated as part of the initial routine clinical evaluation.
目的:骨骼肌损失是恶病质的一个指标,也是某些类型癌症的一个强有力的预后因素。经过严格的标准化,我们旨在评估低肌肉质量(LMM)在常见癌症类型一线化疗中的预测和预后价值。方法:2015 - 2020年在某地区医院进行回顾性单中心研究。诊断为远处转移性癌症的患者如果在一线化疗前45天进行腹部计算机断层扫描,则进行筛查并纳入研究。评估LMM与无进展生存期(PFS)、总生存期(OS)和客观缓解率(ORR)之间的关系。结果:最初,289例转移性癌症患者被纳入研究。中位随访时间17个月,平均年龄61.09±13.03岁(25 ~ 95岁),女性占45.9%。经性别调整后,50.5%的患者有LMM。单因素分析中,LMM与较差的OS和PFS相关(HR:1.598;1.216-2.100;OS和HR的p=0.001:1.583;1.216-2.059;PFS的p=0.001),在诊断和年龄调整后,这种正相关仍然存在。非lmm组呼吸和胃肠道肿瘤、乳腺癌、前列腺癌和妇科肿瘤的orr较好。结论:LMM对多种类型的肿瘤不仅具有预后价值,而且具有预测价值。因此,肌肉损失的评估应作为初始常规临床评估的一部分。
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引用次数: 0
Assessment of Preanalytical Errors by Six Sigma Method and Pareto‘s Principle 用六西格玛法和帕累托原理评价分析前误差
Pub Date : 2023-10-29 DOI: 10.30565/medalanya.1325564
Saniye BAŞAK OKTAY, Ferhat HANİKOĞLU
Aim: In this study, we aimed to evaluate the preanalytical errors over a five year period using the Six Sigma methodology and Pareto Principle in the clinical biochemistry laboratory. Methods: Five-year sample rejection data between January 2015 and December 2019 in the clinical biochemistry laboratory were analyzed and classified according to the reasons for rejection. Six Sigma levels for the total and each preanalytical error were calculated with Westgard online formula. Preanalytical errors were evaluated according to their frequencies ranks and percentages with Pareto's principle. Results: The overall rate of five-year total critical preanalytical errors was 1.91% and the sigma level was 3.6. According to Pareto's chart, the three most common errors among the five-year preanalytical rejections were clotted sample (42.49%, sigma value:4), insufficient sample (23.53%, sigma value:4.2), and wrong container (8.01%, sigma value:4.5). Conclusion: Six Sigma is a quality management methodology used to evaluate laboratory performance processes according to universal quality criteria. Calculated sigma values of preanalytical errors in our laboratory were within the acceptable range. However, planned regulatory activities for frequently observed preanalytical errors should be a laboratory management strategy to reduce these error rates and improve our laboratory performance.
目的:在这项研究中,我们的目的是在临床生物化学实验室中使用六西格玛方法和帕累托原理评估五年期间的分析前误差。方法:对临床生化实验室2015年1月- 2019年12月5年样本拒收数据进行分析,并根据拒收原因进行分类。总误差和分析前误差的六西格玛水平用Westgard在线公式计算。根据帕累托原理对分析前误差的频率、等级和百分比进行评估。结果:5年总临界分析前误差率为1.91%,西格玛水平为3.6。根据帕累托图,在5年的分析前拒收中,最常见的三个错误是样本凝结(42.49%,sigma值为4)、样本不足(23.53%,sigma值为4.2)和容器错误(8.01%,sigma值为4.5)。结论:六西格玛是一种质量管理方法,用于根据通用质量标准评价实验室绩效过程。本实验室分析前误差的sigma计算值在可接受范围内。然而,对于经常观察到的分析前错误,计划的监管活动应该是一种实验室管理策略,以减少这些错误率并提高我们的实验室绩效。
{"title":"Assessment of Preanalytical Errors by Six Sigma Method and Pareto‘s Principle","authors":"Saniye BAŞAK OKTAY, Ferhat HANİKOĞLU","doi":"10.30565/medalanya.1325564","DOIUrl":"https://doi.org/10.30565/medalanya.1325564","url":null,"abstract":"Aim: In this study, we aimed to evaluate the preanalytical errors over a five year period using the Six Sigma methodology and Pareto Principle in the clinical biochemistry laboratory. Methods: Five-year sample rejection data between January 2015 and December 2019 in the clinical biochemistry laboratory were analyzed and classified according to the reasons for rejection. Six Sigma levels for the total and each preanalytical error were calculated with Westgard online formula. Preanalytical errors were evaluated according to their frequencies ranks and percentages with Pareto's principle. Results: The overall rate of five-year total critical preanalytical errors was 1.91% and the sigma level was 3.6. According to Pareto's chart, the three most common errors among the five-year preanalytical rejections were clotted sample (42.49%, sigma value:4), insufficient sample (23.53%, sigma value:4.2), and wrong container (8.01%, sigma value:4.5). Conclusion: Six Sigma is a quality management methodology used to evaluate laboratory performance processes according to universal quality criteria. Calculated sigma values of preanalytical errors in our laboratory were within the acceptable range. However, planned regulatory activities for frequently observed preanalytical errors should be a laboratory management strategy to reduce these error rates and improve our laboratory performance.","PeriodicalId":7003,"journal":{"name":"Acta Medica Alanya","volume":"17 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136134044","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Clinical Detection of Presence and Absence of Palmaris Longus Tendon in Somali Population 索马里人群掌长肌腱有无的临床检测
Pub Date : 2023-10-29 DOI: 10.30565/medalanya.1342908
Hasan MAY, Abdullahi Yusuf MOHAMED
Aim: The aim of this study was to investigate whether the frequency of palmaris longus (PL) absence in Somali population differed from other populations in Africa and the rest of the world and to evaluate its association with sex and side of the limb involved. Methods: Totally 1,000 participants (713 males and 287 females; age range: 7 to 80 years) were tested for the absence of PL tendon using Schaffer’s test. In those with a negative Schaffer's test result, Thompson's test, Mishra's test I, Mishra's test II, and Pushpakumar's "two-finger sign" method were used to confirm its absence. Results: Absence of PL tendon was found in 95 (9.5%) participants. The PL muscle was absent bilaterally in 42 (4.4%) and unilaterally in 53 (5.5%) participants. Unilateral absence of PL was higher in the right hand (3.0%) (p>0.05). Agenesis of the right side in males was significantly correlated with the left side in males (rs=0.556, p<0.01). Right agenesis in females was significantly correlated with its left side (rs=0.625, p<0.01). The incidence of right and left agenesis in females was more strongly correlated than that in males. Age was significantly correlated with left agenesis (rs=0.154, p<0.01) and right agenesis (rs=0.145, p<0.05) in females. Conclusion: The prevalence of PL agenesis in the Somali population is lower than the reported incidence of 15%, but more significantly higher than some of the other African populations. These findings may be helpful, particularly for the surgeons in the region, for orthopedic and reconstructive surgeries using PL grafting.
目的:本研究的目的是调查索马里人群掌长肌(PL)缺失的频率是否与非洲和世界其他地区的其他人群不同,并评估其与性别和受累肢体的关系。方法:共1000名受试者(男性713人,女性287人;年龄范围:7 ~ 80岁),采用Schaffer试验检测左后侧肌腱缺失。在Schaffer测试结果为阴性的患者中,使用Thompson测试、Mishra测试I、Mishra测试II和Pushpakumar的“两指符号”方法证实其不存在。结果:95名(9.5%)参与者发现左后侧肌腱缺失。42例(4.4%)双侧和53例(5.5%)单侧腓骨肌缺失。单侧PL缺失在右侧更高(3.0%)(p>0.05)。男性右侧发育不全与男性左侧发育不全极显著相关(rs=0.556, p<0.01)。雌性右侧发育与其左侧发育极显著相关(rs=0.625, p<0.01)。女性的左右发育不全发生率比男性的相关更强。年龄与女性左侧发育不全(rs=0.154, p<0.01)和右侧发育不全(rs=0.145, p<0.05)显著相关。结论:索马里人群中PL发育的发生率低于报道的15%,但明显高于其他一些非洲人群。这些发现可能有助于,特别是在该地区的外科医生,矫形和重建手术中使用PL嫁接。
{"title":"Clinical Detection of Presence and Absence of Palmaris Longus Tendon in Somali Population","authors":"Hasan MAY, Abdullahi Yusuf MOHAMED","doi":"10.30565/medalanya.1342908","DOIUrl":"https://doi.org/10.30565/medalanya.1342908","url":null,"abstract":"Aim: The aim of this study was to investigate whether the frequency of palmaris longus (PL) absence in Somali population differed from other populations in Africa and the rest of the world and to evaluate its association with sex and side of the limb involved. Methods: Totally 1,000 participants (713 males and 287 females; age range: 7 to 80 years) were tested for the absence of PL tendon using Schaffer’s test. In those with a negative Schaffer's test result, Thompson's test, Mishra's test I, Mishra's test II, and Pushpakumar's \"two-finger sign\" method were used to confirm its absence. Results: Absence of PL tendon was found in 95 (9.5%) participants. The PL muscle was absent bilaterally in 42 (4.4%) and unilaterally in 53 (5.5%) participants. Unilateral absence of PL was higher in the right hand (3.0%) (p&amp;gt;0.05). Agenesis of the right side in males was significantly correlated with the left side in males (rs=0.556, p&amp;lt;0.01). Right agenesis in females was significantly correlated with its left side (rs=0.625, p&amp;lt;0.01). The incidence of right and left agenesis in females was more strongly correlated than that in males. Age was significantly correlated with left agenesis (rs=0.154, p&amp;lt;0.01) and right agenesis (rs=0.145, p&amp;lt;0.05) in females. Conclusion: The prevalence of PL agenesis in the Somali population is lower than the reported incidence of 15%, but more significantly higher than some of the other African populations. These findings may be helpful, particularly for the surgeons in the region, for orthopedic and reconstructive surgeries using PL grafting.","PeriodicalId":7003,"journal":{"name":"Acta Medica Alanya","volume":"57 8","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136134048","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Lack of Association Between FNDC5 Gene Polymorphisms, Serum Irisin Levels and Allergic Rhinitis FNDC5基因多态性、血清鸢尾素水平与变应性鼻炎缺乏相关性
Pub Date : 2023-10-29 DOI: 10.30565/medalanya.1341821
Durkadın DEMİR EKŞİ, Hüseyin GÜNİZİ
Aim: Allergic rhinitis (AR) is an inflammatory nasal mucosa disease caused by type 1 immunoglobulin E-mediated reactions to allergen exposure. Irisin is a hormone released by skeletal muscles in response to exercise. There are studies that demonstrate the relationship of irisin with inflammation. We aimed to investigate the potential association between irisin coding fibronectin type III domain 5 (FNDC5) gene polymorphisms, serum irisin levels, and AR. Method: A case-control study was designed, involving 100 AR patients and 100 healthy controls. Genotyping of rs726344 and rs1746661 SNPs within the FNDC5 gene was performed using PCR-RFLP method. Serum irisin levels were measured using ELISA. Results: Genotyping of rs726344 SNP in patients revealed 90% GG and 10% GA genotypes, while in controls, it was 94% GG and 6% GA. The AA genotype was not detected in any case. For rs1746661 SNP, patients had 57% GG, 39% GT, and 4% TT genotypes, while controls had 58% GG, 36% GT, and 6% TT genotypes. No significant difference was found in rs726344 and rs1746661 SNPs between the patients and the control group. Serum irisin level was 406.3±56.09 ng/ml in patients and 354.3±46.06 ng/ml in controls with no significant difference. Conclusion: This is the first study aiming to investigate the relationship between the irisin protein, its encoding gene, and AR. No significant association was identified between FNDC5 gene polymorphisms, serum irisin levels, and allergic rhinitis. While these findings suggest a limited role of these factors in AR, further studies are needed for more comprehensive understanding of the irisin-AR relationship.
目的:变应性鼻炎(AR)是一种由1型免疫球蛋白e介导的对过敏原暴露的反应引起的炎症性鼻黏膜疾病。鸢尾素是骨骼肌在运动后释放的一种激素。有研究证明了鸢尾素与炎症的关系。我们旨在探讨鸢尾素编码纤维连接蛋白III型结构域5 (FNDC5)基因多态性、血清鸢尾素水平和AR之间的潜在关联。方法:设计了一项病例对照研究,包括100名AR患者和100名健康对照者。采用PCR-RFLP方法对FNDC5基因内rs726344和rs1746661 snp进行基因分型。ELISA法测定血清鸢尾素水平。结果:患者rs726344 SNP基因分型为90% GG和10% GA基因型,对照组为94% GG和6% GA基因型。未检出AA基因型。对于rs1746661 SNP,患者有57% GG、39% GT和4% TT基因型,而对照组有58% GG、36% GT和6% TT基因型。rs726344和rs1746661 snp在患者和对照组之间无显著差异。患者血清鸢尾素水平为406.3±56.09 ng/ml,对照组为354.3±46.06 ng/ml,差异无统计学意义。结论:本研究首次探讨鸢尾素蛋白及其编码基因与AR之间的关系,FNDC5基因多态性、血清鸢尾素水平与变应性鼻炎之间未发现显著相关性。虽然这些发现表明这些因素在AR中的作用有限,但需要进一步的研究来更全面地了解鸢尾-AR的关系。
{"title":"Lack of Association Between FNDC5 Gene Polymorphisms, Serum Irisin Levels and Allergic Rhinitis","authors":"Durkadın DEMİR EKŞİ, Hüseyin GÜNİZİ","doi":"10.30565/medalanya.1341821","DOIUrl":"https://doi.org/10.30565/medalanya.1341821","url":null,"abstract":"Aim: Allergic rhinitis (AR) is an inflammatory nasal mucosa disease caused by type 1 immunoglobulin E-mediated reactions to allergen exposure. Irisin is a hormone released by skeletal muscles in response to exercise. There are studies that demonstrate the relationship of irisin with inflammation. We aimed to investigate the potential association between irisin coding fibronectin type III domain 5 (FNDC5) gene polymorphisms, serum irisin levels, and AR. Method: A case-control study was designed, involving 100 AR patients and 100 healthy controls. Genotyping of rs726344 and rs1746661 SNPs within the FNDC5 gene was performed using PCR-RFLP method. Serum irisin levels were measured using ELISA. Results: Genotyping of rs726344 SNP in patients revealed 90% GG and 10% GA genotypes, while in controls, it was 94% GG and 6% GA. The AA genotype was not detected in any case. For rs1746661 SNP, patients had 57% GG, 39% GT, and 4% TT genotypes, while controls had 58% GG, 36% GT, and 6% TT genotypes. No significant difference was found in rs726344 and rs1746661 SNPs between the patients and the control group. Serum irisin level was 406.3±56.09 ng/ml in patients and 354.3±46.06 ng/ml in controls with no significant difference. Conclusion: This is the first study aiming to investigate the relationship between the irisin protein, its encoding gene, and AR. No significant association was identified between FNDC5 gene polymorphisms, serum irisin levels, and allergic rhinitis. While these findings suggest a limited role of these factors in AR, further studies are needed for more comprehensive understanding of the irisin-AR relationship.","PeriodicalId":7003,"journal":{"name":"Acta Medica Alanya","volume":"57 4","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136134052","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Which scapula fractures should we operate on and what are the functional outcomes? 我们应该对哪些肩胛骨骨折进行手术?手术后的功能结果如何?
Pub Date : 2023-10-29 DOI: 10.30565/medalanya.1358781
İbrahim ETLİ
Aim: In this study we reported the functional results and complications of patients with scapula fractures who underwent open reduction and internal fixation. Methods: The study included 16 patients with scapula fractures who were treated with open reduction and internal fixation(ORIF) between September 2015 and March 2022. Radiologic examination (AP in the scapular plane, lateral and axillary radiography) and computed tomography (CT) scans were performed in all patients. Fractures were classified according to the revised (AO/OTA) classification system. The patients underwent deltopectoral and posterior approaches described by Judet. Functional outcomes were measured using Constant-Murley scores. Results: Ten patients had a scapular neck fracture, or glenoid fossa fracture, five patients had a scapular trunk fracture affecting the glenohumeral joint, and one patient had a scapula process fracture. It was accompanied by clavicle shaft fracture in five patients. The mean follow-up period after injury was 42 months (6-92 months). The mean Constant-Murley score (CMS) for the shoulder with scapula fracture was 93.8 (±8.93). Conclusion: Open reduction and internal fixation of displaced scapular fractures is an effective treatment option in terms of union rate and functional outcome.
目的:在本研究中,我们报道了肩胛骨骨折患者接受切开复位内固定的功能结果和并发症。方法:选取2015年9月至2022年3月间接受切开复位内固定(ORIF)治疗的16例肩胛骨骨折患者。所有患者均行放射学检查(肩胛骨平面AP,侧位和腋窝x线片)和计算机断层扫描(CT)。根据修订后的(AO/OTA)分类系统对骨折进行分类。患者接受了由Judet描述的三角胸后入路。功能结果用Constant-Murley评分来衡量。结果:10例发生肩胛骨颈骨折或肩胛窝骨折,5例发生肩胛骨干骨折累及肩关节,1例发生肩胛骨突骨折。5例伴有锁骨干骨折。伤后平均随访42个月(6 ~ 92个月)。肩胛骨骨折的平均Constant-Murley评分为93.8(±8.93)。结论:开放性复位内固定治疗移位性肩胛骨骨折在愈合率和功能预后方面是一种有效的治疗方法。
{"title":"Which scapula fractures should we operate on and what are the functional outcomes?","authors":"İbrahim ETLİ","doi":"10.30565/medalanya.1358781","DOIUrl":"https://doi.org/10.30565/medalanya.1358781","url":null,"abstract":"Aim: In this study we reported the functional results and complications of patients with scapula fractures who underwent open reduction and internal fixation. Methods: The study included 16 patients with scapula fractures who were treated with open reduction and internal fixation(ORIF) between September 2015 and March 2022. Radiologic examination (AP in the scapular plane, lateral and axillary radiography) and computed tomography (CT) scans were performed in all patients. Fractures were classified according to the revised (AO/OTA) classification system. The patients underwent deltopectoral and posterior approaches described by Judet. Functional outcomes were measured using Constant-Murley scores. Results: Ten patients had a scapular neck fracture, or glenoid fossa fracture, five patients had a scapular trunk fracture affecting the glenohumeral joint, and one patient had a scapula process fracture. It was accompanied by clavicle shaft fracture in five patients. The mean follow-up period after injury was 42 months (6-92 months). The mean Constant-Murley score (CMS) for the shoulder with scapula fracture was 93.8 (±8.93). Conclusion: Open reduction and internal fixation of displaced scapular fractures is an effective treatment option in terms of union rate and functional outcome.","PeriodicalId":7003,"journal":{"name":"Acta Medica Alanya","volume":"31 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136134197","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Prognostic significance of PNI, SIRI and LIPI in non small-cell lung cancer PNI、SIRI和LIPI在非小细胞肺癌中的预后意义
Pub Date : 2023-10-29 DOI: 10.30565/medalanya.1314292
Onur Yazdan BALÇIK, Ali AYTAÇ, Tugay AVCI, Bilgin DEMİR, Yusuf İLHAN, Gökhan KARAKYA, Atike Pinar ERDOĞAN
Aim: Non-small cell lung cancer (NSCLC) is one of the 3 most common and deadly cancers. The aim of the current study is to investigate whether Prognostic Nutritional Index /PNI), Systemic Immune-Inflammation Index (SIRI), Lung Immune Prognostic Index (LIPI) has a prognostic significance in patients with metastatic NSLCL. Methods: Patients diagnosed with pathologically confirmed metastatic NSCLC in 5 different hospitals in Turkey between 2016-2022 were included in our study and analyzed retrospectively. overall survival (OS) and progression-free survival (PFS) were recorded. Results: The median PFS was 5.50 months, while the median OS was 16.03 months. Median OS was 14.86 months for the PNI-Low group and 17.2 months for the PNI-High group (p: &lt;0.121). The median OS of the PNI-Low group was shorter than the PNI-High group, but there was no statistically significant difference between the groups. Median OS was 19.86 months for the SIRI-Low group and 14.23 months for the SIRI-High group (p: &lt;0.112). Median OS was 17.76, 15.13, 13.73 months for the LIPI-Low, LIPI-intermediate group and LIPI-high group, there was no statistically significant difference between the groups (p: &lt;0.391) Conclusion: In conclusion, PNI and SIRI may be significant in a prospective study in a specific patient group to be performed with a larger number of patients to predict the prognosis of patients with metastatic NSCLC.
目的:非小细胞肺癌(NSCLC)是三种最常见和最致命的癌症之一。本研究的目的是探讨预后营养指数(PNI)、全身免疫炎症指数(SIRI)、肺免疫预后指数(LIPI)在转移性非细胞肺癌患者中的预后意义。方法:回顾性分析2016-2022年间土耳其5家不同医院病理确诊的转移性NSCLC患者。记录总生存期(OS)和无进展生存期(PFS)。结果:中位PFS为5.50个月,中位OS为16.03个月。PNI-Low组中位生存期为14.86个月,PNI-High组中位生存期为17.2个月(p: <0.121)。PNI-Low组的中位OS短于PNI-High组,但两组间差异无统计学意义。SIRI-Low组的中位OS为19.86个月,SIRI-High组的中位OS为14.23个月(p: <0.112)。LIPI-Low组、LIPI-intermediate组和LIPI-high组的中位OS分别为17.76、15.13、13.73个月,组间差异无统计学意义(p: <0.391)。结论:PNI和SIRI可能在特定患者组的前瞻性研究中具有显著意义,该研究将对更多患者进行预测转移性NSCLC患者的预后。
{"title":"Prognostic significance of PNI, SIRI and LIPI in non small-cell lung cancer","authors":"Onur Yazdan BALÇIK, Ali AYTAÇ, Tugay AVCI, Bilgin DEMİR, Yusuf İLHAN, Gökhan KARAKYA, Atike Pinar ERDOĞAN","doi":"10.30565/medalanya.1314292","DOIUrl":"https://doi.org/10.30565/medalanya.1314292","url":null,"abstract":"Aim: Non-small cell lung cancer (NSCLC) is one of the 3 most common and deadly cancers. The aim of the current study is to investigate whether Prognostic Nutritional Index /PNI), Systemic Immune-Inflammation Index (SIRI), Lung Immune Prognostic Index (LIPI) has a prognostic significance in patients with metastatic NSLCL. Methods: Patients diagnosed with pathologically confirmed metastatic NSCLC in 5 different hospitals in Turkey between 2016-2022 were included in our study and analyzed retrospectively. overall survival (OS) and progression-free survival (PFS) were recorded. Results: The median PFS was 5.50 months, while the median OS was 16.03 months. Median OS was 14.86 months for the PNI-Low group and 17.2 months for the PNI-High group (p: &amp;lt;0.121). The median OS of the PNI-Low group was shorter than the PNI-High group, but there was no statistically significant difference between the groups. Median OS was 19.86 months for the SIRI-Low group and 14.23 months for the SIRI-High group (p: &amp;lt;0.112). Median OS was 17.76, 15.13, 13.73 months for the LIPI-Low, LIPI-intermediate group and LIPI-high group, there was no statistically significant difference between the groups (p: &amp;lt;0.391) Conclusion: In conclusion, PNI and SIRI may be significant in a prospective study in a specific patient group to be performed with a larger number of patients to predict the prognosis of patients with metastatic NSCLC.","PeriodicalId":7003,"journal":{"name":"Acta Medica Alanya","volume":"17 3","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136134198","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Relationship Between Fatigue, Cognitive Functions, Depression, and Disability in Multiple Sclerosis Patients 多发性硬化症患者疲劳、认知功能、抑郁和残疾的关系
Pub Date : 2023-10-29 DOI: 10.30565/medalanya.1350671
Gökçe ZEYTİN DEMİRAL
Aim : Multiple Sclerosis (MS) is a chronic, progressive, and neurodegenerative disorder of the central nervous system. It frequently leads to symptoms such as disability, cognitive impairment, fatigue, and depression. This study aims to examine the relationship between fatigue, cognitive functions, depression, and disability among individuals with MS. Methods: Seventy-four MS patients were evaluated by using the Cognitive Failure Questionnaire (CFQ) battery. The Expanded Disability Status Scale (EDSS) was used in determining the level of disability, whereas the Fatigue Severity Scale (FSS) and the Beck Depression Inventory (BDI) were utilized in measuring the levels of fatigue and depression, respectively. Results :Moderate positive correlations were found between EDSS and BDI (r1=0.342; p&lt;0.001), between EDSS and FSS (r1=0.392; p&lt;0.001), between CFQ and BDI (r1=0.451; p&lt;0.001), between CFQ and FSS (r1=0.425; p&lt;0.001), and between FSS and BDI (r1=0.424; p&lt;0.001). Conclusion :The results achieved in this study indicate that fatigue and depression increase as disability increases among Multiple Sclerosis patients and cognitive impairment is associated with both depression and fatigue.
目的:多发性硬化症(MS)是一种慢性,进行性,神经退行性中枢神经系统疾病。它经常导致残疾、认知障碍、疲劳和抑郁等症状。本研究旨在探讨多发性硬化症患者疲劳、认知功能、抑郁和残疾之间的关系。方法:采用认知失败问卷(cognitive Failure Questionnaire, CFQ)对74例多发性硬化症患者进行评估。残疾程度采用扩展残疾状态量表(EDSS),疲劳严重程度量表(FSS)和贝克抑郁量表(BDI)分别测定疲劳和抑郁水平。结果:EDSS与BDI呈中度正相关(r1=0.342;p<0.001), EDSS与FSS之间(r1=0.392;p<0.001), CFQ与BDI之间(r1=0.451;p<0.001), CFQ和FSS之间(r1=0.425;p<0.001), FSS和BDI之间(r1=0.424;p&肝移植;0.001)。结论:本研究结果表明,多发性硬化症患者疲劳和抑郁随着残疾程度的增加而增加,认知障碍与抑郁和疲劳均相关。
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Acta Medica Alanya
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