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جستجوی مقالات مرتبط با کلیدواژه « iron deficiency » در نشریات گروه « پزشکی »

  • Fatemeh Ramezani, Elham Khalaf-Adeli *, Ali Zadehmehr
    Background
    Preoperative anemia is associated with increased morbidity and mortality rates among patients undergoing major surgery. This study aimed to investigate the prevalence of preoperative iron deficiency in patients scheduled for cardiac surgery at a cardiovascular medical and research center in Iran.
     
    Methods
    This prospective cross-sectional study was conducted at the Rajaei Cardiovascular Medical and Research Center in Iran between October 2018 and September 2019. A total of 165 patients aged 18 years or older who were scheduled for elective cardiac surgery were included. The prevalence of iron deficiency anemia was determined using several iron parameters: serum iron levels, serum ferritin levels, total iron-binding capacity, transferrin saturation, complete blood count, serum blood urea nitrogen levels, serum creatinine levels, and C-reactive protein. Data were collected from patients' medical records.
     
    Results
    A total of 165 patients were included in the study, with a male-to-female ratio of 1.3:1. The mean age was 60.6±9.9 years. The prevalence of anemia was 52.1%, higher in women than in men (55.8% vs 44.2%). Iron deficiency anemia was the most common type (75.6%), followed by anemia of chronic disease (15.1%) and other types (9.3%). Iron deficiency anemia was more prevalent in women (60%) than in men (24.7%), whereas anemia of chronic disease was more frequent in men (11.8%) than in women (2.9%).
     
    Conclusions
    Our study revealed a high prevalence of anemia among cardiac surgery patients, particularly iron deficiency anemia. These findings emphasize the importance of preoperative anemia screening and management in cardiac surgery settings, which has significant implications for patient care. (Iranian Heart Journal 2024; 25(3): 21-26)
    Keywords: Iron Deficiency, Cardiovascular Surgery, Anemia}
  • Akram Hemmatipour, Bijan Kikhaei, Razieh Jalkani, Mansour Ahmadnejad, Farhad Soleimanzadeh, Dariush Rokhafrooz *
    Background

    We aimed to determine the level of serum vitamin D and serum ferritin in four groups’ children and adolescents.

    Methods

    This descriptive/analytical study was conducted in 2019 on children and adolescents with thalasse-mia aged 7-18 years in Ahvaz, Iran. Overall, 160 patients with the target inclusion and exclusion criteria were assigned into four groups (n=40) of people withthalassemia minor, thalassemia major, iron deficiency anemia and healthy individuals. The level of ferritin and vitamin D was assessed. Mann-Whitney test, Wilcoxon test and Spearman's correlation test were used as well as SPSS Statistics V21.

    Results

    Themean age of the participants was 13.07 ± 3.82 yr and 100 people (62.5%) were male. In terms of vitamin D deficiency, 16 people (40%) had severe deficiency in iron deficiency group. The highest level of ferri-tin was found in thalassemia major group and thelowest in iron deficiency group. Regarding the level of vita-min D and ferritin in the healthy group, there was a statistically significant difference between mean vitamin D and serum ferritin levels (P=0.027). In iron deficiency group, this level of ferritin was observed with mild defi-ciency (P=0.017). In thalassemia major group, the increase in ferritin was associated with severe vitamin D de-ficiency (P=0.05.

    Conclusion

    Severe vitamin D is seen in thalassemia major due to the increase in ferritin, but moderate defi-ciency of this vitamin in healthy people and mild deficiency in iron deficiency anemia group was observed con-sidering the normal levels of ferritin.

    Keywords: Vitamin D, Ferritin, Thalassemia Minor, Thalassemia Major, Iron Deficiency}
  • Mohammed Fabin, Jayakrishnan Jayakumar, Swathy Shanker*
    Introduction

    Anemia is defined as a reduced hemoglobin content leading to minimized oxygen carrying capacity of the cell. Children are commonly affected by anemia which causes impaired development and cognitive defects in them. Among all the causes, iron deficiency is one of the most important contributing factors to the development of anemia. The prevalence of anemia varies in different regions. This study aims to find the prevalence of anemia among children in an urban population of Kerala.

    Materials and Methods

    This was a retrospective observational study involving 192 children. The children were diagnosed as anemic if hemoglobin value was less than 11g/dl for those younger than 5 years and less than 11.4g/dl in those aged 5-11 years. The children were further diagnosed with mild, moderate or severe anemia based on their hemoglobin levels. Data were retrieved from the hematology reports and tabulated in Microsoft Excel. Analyses were done using SPSS software version 16.0.

    Results

    This study showed the prevalence of anemia to be 54.7%. The majority of anemic children (48.6% ) were mildly anemic while 34.3% were moderately anemic, with 17.1% being severely anemic.

    Conclusion

    In spite of active policy implementation for elimination of anemia, the prevalence of anemia continues to be high indicating the need for active intervention with early detection and treatment of anemia as a routine procedure.

    Keywords: Anemia, Prevalence, Iron Deficiency, Northern Kerala}
  • محمدپویا سمیعی، آزیتا چگینی*، مجید شهابی، امیر تیمورپور
    سابقه و هدف

    اهداکنندگان مستمر به دلیل اهدای مکرر خون، ممکن است به کمبود آهن در بدن دچار شوند. تفاوت های ژنتیکی ممکن است بر کمبود آهن در اهداکنندگان مستمر خون تاثیرگذار باشند. برخی از این ژن ها شامل ژن هایی هستند که در فعالیت های مرتبط با جذب و انتقال آهن در خون نقش دارند. در مطالعه حاضر ارتباط پلی مورفیسم تک نوکلئوتیدی ژن TMPRSS6 (rs855791 V736A) با میزان آهن در اهداکنندگان مستمر مرد مورد بررسی قرار گرفت.

    مواد و روش ها

    این مطالعه از نوع مقطعی بوده و 130 اهداکننده مستمر مرد در آن شرکت داشتند. آزمایش های CBC با استفاده از دستگاه Sysmex K1000 ، آهن سرم با استفاده از روش کالریمتری، فریتین با استفاده از روش الایزا و TIBC با استفاده از روش مستقیم بر روی نمونه خون آن ها انجام شد. ژنوتیپ پلی مورفیسم های مورد نظر با استفاده از روش Allele specific PCR تعیین شد. تمامی داده های جمع آوری شده به وسیله نرم افزار R تحت تجزیه و تحلیل آماری قرار گرفتند. سطح معناداری در این مطالعه 05/0 در نظر گرفته شد.

    یافته ها

    میانگین سنی اهداکنندگان مستمر مورد مطالعه 45 سال با انحراف معیار 5/10 بود. از بین 130 نفر اهداکننده مستمر خون، 28 نفر (54/21 درصد) حامل آلل هموزیگوت T/T، 29 نفر (31/22 درصد) حامل آلل هموزیگوت C/C و 73 نفر (15/56 درصد) حامل آلل هتروزیگوت C/T بودند. ارتباط معنا دار بین پلی مورفیسم rs855791 و شاخص های ارزیابی آهن مشاهده نشد.

    نتیجه گیری

    پلی مورفیسم تک نوکلئوتیدی ژن TMPRSS6 (rs855791 V736A) با سطح آهن و کمیت های مرتبط با آن در اهداکنندگان مستمر خون ارتباط ندارد.

    کلید واژگان: اهداکنندگان خون, کم خونی فقر آهن, پلی مورفیسم (ژنتیک)}
    M.P. Samiee, A. Chegini*, M. Shahabi, A. Teimourpour
    Background and Objectives

    Regular blood donors may experience iron deficiency due to repeated blood donation. Genetic differences might have an impact on iron deficiency in regular blood donors. Some of these genes include those involved in activities related to iron absorption and transfer in blood. In this study, the association of the rs855791 single nucleotide polymorphism in TMPRSS6 gene with iron levels in male regular blood donors was investigated.

    Materials and Methods

    In this cross-sectional study, 130 male regular blood donors participated. CBC tests, serum iron, ferritin, and Total Iron Binding Capacity (TIBC) were performed on their blood samples. The genotypes of the target polymorphisms were determined using the allele-specific PCR method. All collected data were analyzed using R software for statistical analysis.

    Results

    The average age of the regular male blood donors was 45 years with a standard deviation of 10.5. Among the 130 regular blood donors, 28 individuals (21.54%) were homozygous for the T/T allele, 29 individuals (22.31%) were homozygous for the C/C allele, and 73 individuals were heterozygous for the C/T allele. No significant association was observed between the rs855791 single nucleotide polymorphism and iron assessment indicators.

    Conclusions 

    Single nucleotide polymorphism of TMPRSS6 gene (rs855791 v736A) was not associated with iron level and related quantities in regular blood donors.

    Keywords: Blood Donors, Anemia, Iron-Deficiency, Polymorphism (Genetic)}
  • *Seyyed Ali Pirzadeh, Taghi Amiriani, Sima Besharat, Alireza Norouzi, Haniyeh Mirkarimi, NesaShokouhifar, Gholamreza Roshandel, Amrollah Sharifi
    Aim

    This study aimed to assess the status of iron stores and the frequency of iron deficiency anemia in Celiac disease (CD) patients referred to the Golestan Research Center of Gastroenterology and Hepatology, Gorgan, Iran.

    Background

    Studies have shown that nutritional deficiencies affect 20-38% of patients with CD due to malabsorption and as a result of a gluten-free diet.

    Methods

    In this study, 59 out of 100 CD patients were assessed. The presence and severity of anemia were determined using the concentration of serum hemoglobin according to WHO criteria. The status of body iron stores was also assessed based on serum ferritin levels.

    Results

    Mean and SD of age, duration of disease, serum hemoglobin, ferritin, TIBC, and serum iron were 39.9±11.9 years, 69.8±45.4 months, 12.6±1.99 g/dl, 54.3±55.3 mg/dL, 365.9±49.1 μg/dL, and 84.1±37.1 μg/dL, respectively. 68.42% had no anemia, 19.3% had mild anemia, 8.77% had moderate anemia, and 3.51% had severe anemia. 25.42% of patients had depleted iron stores, 71.19% had normal iron stores, and 3.39% were exposed to iron overload. There was a statistically significant correlation between serum hemoglobin and the duration of disease diagnosis (P=0.037, r=0.302).

    Conclusion

    In this study, 31.58% of CD patients on a gluten-free diet had some degree of anemia. In addition, 25.42% of patients had depleted iron stores. These results suggest that CD patients should be evaluated for iron status, even with a gluten-free diet.

    Keywords: Celiac disease, Iron deficiencies, Anemia, Iron-deficiency, Ferritins, Diet, Gluten-free, Nutrition assessment}
  • ارمغان کاظمی نژاد، امیررضا اسپهبدی، فرهاد غلامی، جمشید یزدانی چراتی، پارمیدا گوران*
    سابقه و هدف

    خارش مرتبط با بیماری مزمن کلیوی یا خارش اورمیک، علامتی شایع در افراد با بیماری کلیوی پیشرفته می باشد. تا به حال هیچ ایده روشنی درباره پاتوژنز این خارش یافت نشده است. لذا مطالعه حاضر با هدف بررسی رابطه خارش در بیماران تحت همودیالیز با سطح آهن سرم، فریتین، ظرفیت کل اتصال آهن خون و درصد اشباع ترانسفرین، انجام پذیرفت.

    مواد و روش ها

    در این مطالعه مقطعی توصیفی- همبستگی، 112 بیمار تحت همودیالیز در مراکز دیالیز بیمارستان رازی قایم شهر و شهروند ساری تحت بررسی قرار گرفتند. وجود خارش و شدت آن به وسیله پرسش نامه و با مقیاس آنالوگ بصری یا Visual Analogue Scale (VAS) سنجیده شد. اطلاعات دموگرافیک شامل سن، جنس، بیماری های زمینه ای، اطلاعات مربوط به دیالیز و نتایج آزمایشگاهی شامل اوره، کراتینین، پتاسیم، کلسیم، فسفر، آلکالین فسفاتاز، هورمون پاراتیرویید، هموگلوبین، آلبومین، آهن سرم، فریتین، ظرفیت کل اتصال آهن خون و درصد اشباع ترانسفرین ثبت گردید.

    یافته ها

    از 112 بیمار مورد بررسی، 38 بیمار (33/9 درصد) مورد خارش مرتبط با بیماری مزمن کلیوی بودند و 74 بیمار (66/1 درصد) طی شش ماه اخیر خارشی را ذکر نمی کردند. رابطه بین وجود خارش با متغیرهای جمعیت شناختی، اطلاعات مربوط به دیالیز و متغیرهای آزمایشگاهی در بیماران مورد بررسی تحت همودیالیز معنی دار نشد. همچنین هیچ کدام از مولفه ها ارتباط معنی دار با میزان شدت خارش نداشتند (0/05>p).

    استنتاج

    در این مطالعه رابطه معنی دار بین وجود و شدت خارش با هیچ یک از متغیرهای جمعیت شناختی و پاراکلینیکی در بیماران همودیالیزی مشاهده نشد و فرضیه نقش فقر آهن و آنمی در ایجاد خارش در بیماران تحت همودیالیز رد شد.

    کلید واژگان: خارش, بیماری مزمن کلیوی, همودیالیز, آنمی, فقر آهن}
    Armaghan Kazeminejad, Amirreza Espahbodi, Farhad Gholami, Jamshid Yazdani Charati, Parmida Gouran*
    Background and purpose

    Chronic kidney disease-associated pruritus (CKD-aP) is a common symptom in patients with end-stage renal disease. So far, no clear explanation has been found about the pathogenesis of CKD-aP. Therefore, the present study aimed at investigating the relationship between pruritus in hemodialysis patients and serum iron, ferritin, total iron binding capacity, and transferrin saturation.

    Materials and methods

    In this cross-sectional descriptive correlational study, 112 patients in hemodialysis clinics at Ghaemshahr Razi Hospital and Sari Shahrvand Clinic were investigated. The presence of pruritus and its severity were measured by a questionnaire and Visual Analogue Scale (VAS), respectively. Demographic information including age, gender, underlying diseases, dialysis information, and laboratory data, including urea, creatinine, potassium, calcium, phosphorus, alkaline phosphatase, parathyroid hormone, hemoglobin, albumin, serum iron, ferritin, total iron binding capacity, and transferrin saturation were recorded.

    Results

    Out of 112 patients, 38 (33.9%) had CKD-aP and 74 patients (66.1%) did not report pruritus during the last six months. Findings showed no significant relationships between pruritus and its severity and demographic variables, information related to dialysis, and laboratory results (P> 0.05).

    Conclusion

    We found no significant relationship between the presence and intensity of pruritus and demographic and paraclinical variables in hemodialysis patients, through which the hypothesis of the role of iron deficiency and anemia in causing pruritus in hemodialysis patients was rejected.

    Keywords: pruritus, chronic kidney disease, hemodialysis, anemia, iron deficiency}
  • رضا عباسی*، احمد مختاری، فرناز سادات جوانمردی
    زمینه و هدف

    تشنج ناشی از تب شایعترین اختلال تشنجی در طی دوره کودکی است. به منظور جلوگیری از تشنج تب و عود آن، شناخت عوامل موثر در ایجاد آن اهمیت دارد. با توجه به شیوع بالای تشنج ناشی از تب و آنمی فقر آهن در کودکان و با توجه به این که آنمی فقر آهن یک عامل خطر احتمالی برای وقوع تشنج ناشی از تب است و همچنین اختلاف نظر در مطالعات قبلی در این زمینه، در این مطالعه به بررسی ارتباط آنمی فقر آهن با تشنج ناشی از تب در کودکان پرداخته شد.

    روش بررسی

    مطالعه حاضر یک مطالعه موردی-شاهدی است که به بررسی ارتباط تشنج ناشی از تب در 150 بیمار شش ماه تا پنج سال تب دار بستری در بیمارستان امام سجاد یاسوج که از فروردین تا مرداد 1392 مراجعه کرده اند، می پردازد. در این مطالعه 75 بیمار با تشنج ناشی از تب (گروه مورد) و 75 بیمار تب دار بدون تشنج (گروه شاهد) باهم مقایسه شدند.

    یافته ها: 

    میانگین سنی جمعیت مورد مطالعه 14±4/21 ماه بود. 7/34% از جمعیت مورد مطالعه را زن و 3/65% را مرد تشکیل می دادند. در این مطالعه 7/10% از گروه مورد و 8% از گروه شاهد دچار آنمی فقر آهن بودند. هرچند که شیوع آنمی فقر آهن در گروه تشنج ناشی از تب بیشتر بود، اما این اختلاف معنادار نبود (58/0=P).

    نتیجه گیری: 

    براساس یافته های این مطالعه آنمی فقر آهن به عنوان عامل خطر احتمالی برای تشنج به دنبال تب مطرح نیست.

    کلید واژگان: آنمی, تشنج ناشی از تب, فقر آهن}
    Reza Abbasi*, Ahmad Mokhtari, Farnaz Sadat Javanmardi
    Background

    Febrile seizures (FS) are the most common cause of seizure in children. In order to prevent FS and their recurrence, the recognition of the related factors to recurrence of FS is important. According to the high prevalence of FS and iron deficiency anemia (IDA) in children and that IDA is a possible risk factor for FS, as well as controversies in previous studies in this field, in this study, the relationship between iron deficiency anemia and FS in children was investigated.

    Methods

    This is a case-control study that investigates the relationship between febrile seizures with anemia in 150 patients aged six months to five years with fever who were admitted to Imam Sajjad Yasouj Hospital, from April to August of 2014. In this study, 75 patients with febrile seizures (case group) and 75 febrile patients without seizures (control group) were compared. Cause of fever (urinary infection, gastrointestinal infections, upper respiratory infection, lower respiratory infection and other causes), Information about blood cell count (white blood cell (WBC) and red blood cell (RBC), hemoglobin (HB), mean red blood cell volume (MCV) and serum ferritin level in patients with hemoglobin below 11 were recorded.

    Results

    The mean age of the study population was 21.4 14 months. 34.7% of the study population were girls and 65.3% were boys. In this study, 10.7% of the cases and 8% of the controls had IDA. Although the prevalence of IDA was higher in the FS group, this difference was not significant (P=0.58). Also, HB and MCV were not significantly different in the two groups (P=0.49, P=0.69). In addition, the mean serum ferritin level in the FS group with anemia and the FS group with anemia did not show a statistically significant difference (P=0.94).

    Conclusion

    According to the result of this study, IDA is not a risk factor for seizures in febrile children.

    Keywords: : anemia, febrile seizure, iron deficiency}
  • مهسا امیری حسینی، فاطمه کشاورزی*، ناهید حق نظری
    زمینه و هدف

    آهن یک ماده معدنی ضروری برای زندگی است و تقریبا هر سازمان زنده ای به آهن نیاز دارد. فقر آهن شایع ترین کم خونی در سراسر جهان با پیامدهای مهم بالینی است. این بیماری ناشی از در دسترس نبودن آهن کافی برای تولید هموگلوبین به دلایلی از جمله فقر آهن در رژیم غذایی ،جذب ناکافی آهن، خونریزی مزمن و عوامل ژنتیکی است. چندین پلی مورفیسم ژنتیکی مرتبط با وضعیت آهن با استفاده از مطالعات مرتبط با ژنوم شناسایی شده است. هدف از این مطالعه بررسی پلی مورفیسم های TMPRSS6rs2111833 در مبتلایان به فقرآهن در غرب ایران است.

    روش کار

    تحقیق حاضر یک مطالعه مورد - شاهدی است. نمونه گیری در یک فاصله زمانی 3 ماهه در زمستان 1399 و با همکاری آزمایشگاه های خصوصی در سطح شهر سنندح، دهگلان و کرمانشاه انجام شد. در مجموع 91 نفر با رضایت شخصی انتخاب شده و در این مطالعه قرار گرفتند. از این تعداد براساس نتایج فریتین و همچنین توجه به پارامترهای RBC، WBC ها و پلاکت ها  43 نفر افرادی با فقر آهن و 48 نفر کنترل سالم انتخاب شدند. از هر شرکت کننده 5 میلی لیتر خون اخذ شد و به لوله های CBC حاوی ماده ضد انعقاد انتقال یافت. بعد از استخراج DNA؛ فراوانی آللی پلی مورفیسم مورد نظر افراد با استفاده از تکنیک ARMS-PCR بررسی شد. در انتها آزمون آماری برای مقایسه فراوانی آللی در نمونه های شاهد و افرادی با فقر آهن با استفاده از ابزار SPSS ویندوز انجام شد و مقدار 05/0 p < از نظر آماری توصیف شد.

    یافته ها

    افرادی با فقر آهن 25/47 و افراد سالم 75/52 درصد افراد مورد بررسی را تشکیل دادند. در مجموع  فراوانی GG، AG و AA  در کل شرکت کنندگان بترتیب 45، 22 و 33 درصد بود. از این میزان سهم افرادی با فقر آهن و سالم برای 3 ترادف آللی به ترتیب47 و 44 درصد،  23 و 21 درصد و 30 و 35 درصد بود. همچنین از مجموع 182 آلل، 102 آلل معادل 56 درصد آلل ها G و 80 آلل معادل 44 درصد آلل A بود. سهم آلل G در افرادی با فقر آهن و گروه کنترل به ترتیب 58 و 54 درصد و سهم آلل A 42 و 46 درصد بود. همچنین آزمون هاردی-وینبرگ نشان داد که جمعیت مورد ارزیابی در این تجزیه و تحلیل متعادل است. تمام مدل های ممکن هم بارز، بارز، مغلوب و فوق بارز بررسی شد و در تمام موارد میزان Pv بزرگ تر از  05/0 بود که نشان از عدم وابستگی این پلی مورفیسم با  فقر آهن در جمعیت مورد بررسی داشت.

    نتیجه گیری

    پلی مورفیسم rs2111833 ارتباط معنی داری با فقر آهن در جمعیت مورد بررسی نشان نداد. علاوه بر این، هیچ ارتباط معنی داری بین این پلی مورفیسم و پارامترهای بالینی هموگلوبین، آهن، فریتین، RBC ها، WBC ها و پلاکت ها مشاهده نشد.

    کلید واژگان: فقر آهن, کم خونی, TMPRSS6, rs2111833}
    Mahsa Amiri Hosseini, Fatemeh Keshavarzi*, Nahid Haghnazari
    Background & Aims

    Iron deficiency anemia is the most common anemia worldwide with significant clinical consequences. The disease is caused by not having enough iron to produce hemoglobin for reasons such as dietary iron deficiency, insufficient iron absorption, chronic bleeding, and genetic factors. Hepcidin protein is the main regulator of systemic iron homeostasis hormone ferroportin. The role of hepcidin is to control the expression of iron-releasing ferroportin levels in duodenal cells and macrophages, modulating iron uptake and recycling. Hepcidin inactivation causes severe iron overload, while increased hepcidin causes anemia. Several factors regulate hepcidin synthesis, including matriptase-2, which reduces hepcidin synthesis. Matryptase-2 is a type 2 membrane serum proteinase, encoded by the TMPRSS 6 gene. This gene is located on the long arm of chromosome 22 and is mainly expressed in the liver. In humans, inactivation of this protein leads to a rare autosomal recessive disease called IRIDA. Several genetic polymorphisms related to iron status have been identified using genome-related studies. The aim of this study was to investigate the polymorphism of TMPRSS6rs2111833 in patients with iron deficiency anemia in the west of the country.

    Methods

    The present study is a case-control study. Using the sample size determination method available, sampling was performed at a time interval of 3 months with the cooperation of private laboratories in Sanandaj, Dehgolan and Kermanshah. A total of 91 people were randomly included with respect personal consent. Of these, according to the results of ferritin, hemoglobin, red blood cells, white blood cells and platelets 43(47.25%) with iron deficiency anemia and 48(52.75%) healthy controls were enrolled. Five ml of blood sample was collected from all participants and placed in CBC tubes containing anticoagulant and after inverting several times, it was placed in freezer -20. DNA extraction was performed using the extraction kit of Kwsar Company and according to the kit instructions. The quantity and quality of the extracted DNAs were determined using light absorption in spectrophotometer and electrophoresis on 1% agarose gel. The isolated DNA was stored in separate microtubes at -20 ° C until PCR. Then the genotype of individuals was obtained using ARMS-PCR technique and primer sequences used in previous studies. Amplification of the desired fragment was performed using Sinagene Company PCR kit by Rotor-Gene Q (Corbett Life Science) cyclotron device according to the protocol and the PCR product was loaded on 1.8% agarose gel and the quantity and quality were determined. Finally, a statistical test was performed to compare the frequency of genotypes in all samples using Windows SPSS tool and the value of p <0.05 was statistically described.

    Results

    The results showed that the frequency of GG, AG and AA in all participants were 45%, 22% and 33%, respectively, and so for sick and healthy individuals were 47 and 44, 23 and 21 and 30 and 35, respectively. Also, out of 200 alleles, 120(56%) and 80(44%) alleles were G and A, respectively. The portion of G allele in patients and controls group was 58 and 54% and the share of A allele was 42 and 46%, respectively. Hardy Weinberg and heterozygosity equilibria were also examined for the two groups. The Hardy-Weinberg test showed that the assessed population was balanced. Heterozygosity for a gene locus is defined as the frequency of heterozygous individuals for that locus relative to the total population. A gene locus is polymorphic if its heterozygosity is greater than 0.1, and if it is greater than 0.7, it is highly polymorphic. Based on the results of this study, it was seen that the difference between observed and expected heterozygosity in the studied polymorphism is less than 0.1, so the gene position is not polymorphic. Also, co-dominant, dominant, recessive and super-dominant models were examined and in all cases, the Pv value was greater than 0.05. On the other hand, Sixty-nine percent of participants had normal hemoglobin, 41% normal iron, 51% normal ferritin, 83% normal red blood cells, 92% normal platelets and 82% normal white blood cells. On the other hand, 22% of participants had abnormal hemoglobin, 65% abnormal iron, 54% abnormal ferritin, 22% abnormal red blood cells, 2% abnormal platelets and 26% abnormal white blood cells. rs 2111833 showed no significant association with decreased serum hemoglobin, serum iron, serum ferritin, platelets, red and white blood cells.

    Conclusion

    This results showed that the rs2111833 polymorphism were not significantly associated iron deficiency anemia in the studied population. In addition, no significant association was found between rs2111833 and hemoglobin, iron, ferritin, platelets, RBCs and WBCs clinical parameters. Beutler and colleagues investigated the role of TMPRSS6 gene polymorphisms in adults with iron deficiency anemia. Their observations highlighted the role of matriptase-2 in controlling iron metabolism and erythrocyte parameters. Sylvester et al. Reported the association of TMPRSS6 mutations with iron deficiency anemia. Previously, Feinberg et al. reported several mononucleotide polymorphisms associated with iron deficiency anemia, including rs 869320724, rs 767094129, rs 786205059, rs 137853120 and rs 137853119.7 Several studies have shown that the polymorphism rs 2111833 is associated with decreased iron and hemoglobin levels therefore, it related with an increased risk in iron deficiency anemia.  In 2015, Gichohi-Wainaina et al. Identified some changes in the partial frequencies of the rs 2111833 alleles in Asian populations compared to the Caucasian population, which matched our findings. Anemia remains a widespread and significant global health problem that needs to be adequately addressed. Although iron deficiency anemia is the leading cause of anemia in most areas, recent research shows that the cause of anemia is complex and specific to each region. To better understand how to help the underlying causes of anemia, including iron deficiency anemia and other nutritional deficiencies, diseases, and hemoglobin disorders, efforts need to be made to make appropriate interventions work under certain conditions. Further studies on a larger patient scale are also necessary to identify potential haplotypes and polymorphisms responsible for the low response to oral iron therapy and may be useful for planning a proper iron supplementation.There were some limitations to this study, such as an insufficient total number of participants. However, these results could enhance our understanding of the role of genetics, particularly single nucleotide polymorphisms, in increasing susceptibility to a variety of diseases.

    Keywords: Iron Deficiency, Anemia, TMPRSS6, rs2111833}
  • Devesh Yerrapragada, Rashmi N
    Background and Objective

     To our knowledge in our country not many studies have been done regarding the iron status and cognitive function in children. Therefore, the aim of this study was to investigate the relationship between serum iron levels and cognitive function in children aged 1 month to 5 years in our institution.

    Methods

     This study was conducted for 18 months in the pediatric population of a tertiary care hospital in Mysore, India, after obtaining approval from the Ethics Committee of the institution. A total of 255 subjects aged between 1 month and 5 years were selected as per the eligibility criteria. From these children, a venous blood sample was sent for determination of iron levels and total iron binding capacity. Cognitive abilities were assessed using the age-appropriate Ages and Stages Questionnaire (ASQ -3).

    Findings

     The mean age of the study population was 22.87±14.83 months and the male-to-female ratio was 1.7:1. Totally, 230 out of 255 children were iron deficient (90.2%), 91.3% boys and 88.3 % girls. Anemia was found in 55.7% of the children, with 94.3% of those with anemia suffering from ID. ID was found to have a negative significant effect on fine motor skills (p < 0.0001) and problem-solving ability (p=0.01). Gross motor skills were significantly impaired by ID (p<0.0001).

    Conclusion

     This study re-emphasizes that ID and IDA have a negative impact on cognitive development and performance, with more severe effects in the last stage of ID –IDA.

    Keywords: Ages, Stages Questionnaire, Cognitive Development, Cognitive Skills, Iron, Iron Deficiency, Iron-Deficiency Anemia}
  • Narjes Amrollahi *, MohammadJavad Tarrahi

    Context:

     Dental caries is a complication affecting the health of society, so it is vital to manage. Most children with early childhood caries (ECC) are believed to undergo anemia, altered physical growth patterns, and low weight.

    Objectives

     This study aimed to evaluate the relationship between dental caries and iron deficiency anemia (IDA) in children.
    Evidence Acquisition: The medical subject headings (MeSH) and non-MeSH were applied to choose the search terms. English language case-control studies assessing blood factors associated with IDA in children with and without dental caries were potentially eligible. Two independent researchers carried out an electronic search to retrieve studies published in the English language on Scopus, ProQuest, PubMed, and Web of Science databases in October 2020. Initially, 494 articles were obtained. Of them, 17 were eligible for inclusion, of which eight studies were eliminated. The meta-analysis was done using the comprehensive meta-analysis software (version 2, Biostat). The forest plots estimated the mean difference and depicted the results of the meta-analysis. The Egger's and Begg's tests assessed the publication bias.

    Results

     A significant difference was observed in serum ferritin levels between the case and control groups, with a mean difference of -0.230 (95% confidence interval (CI): -0.446 to -0.015; P value = 0.008). Blood hemoglobin and mean corpuscular volume (MCV) levels indicated significant mean differences of -0.991 (95% CI: -1.813 to -0.169) and -0.807 (95% CI: -1.336 to -0.279), respectively (P value < 0001). In the case group, all three blood parameters were significantly lower.

    Conclusions

     Hemoglobin, serum ferritin, and MCV levels are lower in children with dental caries than in caries-free children.

    Keywords: Iron Deficiency, Anemia, Dental Caries, Child}
  • Hanan Hanna, Amany Salama

    Obesity/its comorbidities occasionally exist alone, but actually, this is a dynamic network of cross morbidities that are often regarded as separable entities. Obesity is nowadays viewed as an escalating risk factor for iron deficiency, and various theories have been proposed since then explaining their relation. We aimed to determine the relationship of increased body mass index (BMI) with adiponectin, leptin, and iron profile in a sample of middle-aged and older adults with and without iron deficiency anemia. An observational study was performed among 90 participants classified into three groups. Group І included healthy subjects with normal BMI; as a control. Group II included subjects with increased BMI, and group III included subjects with increased BMI and iron deficiency anemia. After overnight fasting, fasting blood glucose, triglycerides, total cholesterol, iron, total iron-binding capacity, complete blood count, serum leptin, and adiponectin were measured. There were significantly higher mean values of BMI among those with anemia, higher mean values of serum leptin, and significantly lower mean values of adiponectin. A significant positive correlation of serum leptin with BMI and a significant negative correlation of serum leptin with iron in Group III were reported. The adiponectin/leptin ratio of (0.8) was correlated with iron and homeostatic model assessment in Group III, and a ratio of (1.1) was significantly correlated with BMI and hemoglobin level in Group II. This could suggest that interventions aimed at increasing the adiponectin/leptin ratio may help in resolving anemia among obese populations by increasing their serum iron and hemoglobin.

    Keywords: Obesity, Iron deficiency, Adiponectin, Leptin, leptin ratio}
  • رامین تقی زاده، مجتبی خادم الحسینی، ایوب شیرزادی، لیلا جانانی، فاطمه السادات امیری*
    زمینه و هدف

    کم خونی شایع ترین اختلال دوران بارداری است و تقریبا 75% از آن مربوط به آنمی فقر آهن می باشد. در مادران با افت هموگلوبین احتمال زایمان زودرس و محدودیت رشد جنین افزایش مییابد. این مطالعه به منظور تعیین میزان کم خونی فقر آهن در زنان باردار مراجعه کننده به مراکز بهداشت شهر فردیس انجام شده است.

    مواد و روش ها

    در این مطالعه توصیفی مقطعی که در طول شش ماهه اول سال  1397 انجام شد پرونده 402 زن که به مراکز بهداشت شهر فردیس مراجعه کرده و حاملگی خود را به پایان رسانده بودند مورد بررسی قرار گرفت. داده های آزمایشگاهی و دموگرافیکی  این مطالعه براساس معیار های مراقبت دوران بارداری و پیش از بارداری سازمان بهداشت جهانی و با استفاده از پرسشنامه و نیز اطلاعات سامانه سیب جمع آوری شده است. برای بررسی روابط بین متغیرها از آمون های آماری مجذور کای ، تی تست و اسپیرمن استفاده گردید.

    یافته ها

    میزان شیوع آنمی در این مطالعه در سه ماهه اول بارداری 5% و در سه ماهه سوم 5/13% بود. میان سن ، وزن پیش از بارداری ، شاخص توده بدنی در گروه مبتلا به کم خونی و بدون کم خونی تفاوت معنا داری یافت نشد. میان فاصله از آخرین زایمان و تعداد بارداری با سطح هموگلوبین رابطه معکوس معناداری ملاحظه گردید. همچنین مشخص شد افرادی که در سه ماهه اول بارداری دچار کم خونی بودند به شکل معنا داری وزن گیری بیشتری طی دوران بارداری داشتند.

    نتیجه گیری

    با توجه به یافته ها ، شیوع کم خونی به ویژه در سه ماهه سوم ناخوشایند بود. از آنجا که این اختلال تغذیه ای قابل پیشگیری است ، توجه به گسترش مراقبت های قبل از بارداری و افزایش آگاهی مادران نسبت به تغذیه مناسب و استفاده از مکمل ها در صورت نیاز ضروری است.

    کلید واژگان: کم خونی, فقر آهن, زنان باردار}
    Ramin Taghizadeh, Mojtaba Khadem Al-Hosseini, Ayub Shirzadi, Leila Janani, Fatemehsadat Amiri*
    Background and objectives

    Anemia is the most common disorder during pregnancy and approximately 75% of it is related to iron deficiency anemia. Decreased hemoglobin levels increase premature delivery and can lead to intrauterine growth restriction. This study was performed to determine the rate of iron deficiency anemia in pregnant women referring to health centers in Fardis.

    Methods

    In this cross-sectional descriptive study conducted in 2018, the health records of 402 women who referred to health centers in Fardis and completed their pregnancies were examined. The data of this study were collected according to the criteria of the World Health Organization and using the information of the Sib system. Chi-square and t-test statistics were used to investigate the relationships between variables.

    Results

    The prevalence of anemia in this study was 5% in the first trimester of pregnancy and 13/5% in the third trimester. No significant difference was found between age, pre-pregnancy weight, and body mass index in the group with and without anemia. There was a significant inverse relationship between the distance from the last delivery and the number of pregnancies with the hemoglobin level. It was also found people who were anemic in the first trimester of pregnancy, during pregnancy had a significantly greater weight gain.

    Conclusion

    According to the results, the prevalence of anemia was especially unpleasant in the third trimester. Because this eating disorder is preventable, it is important to pay attention to expanding pre-pregnancy care and increasing mothers' awareness of proper nutrition and supplementation as needed.

    Keywords: Anemia, Iron deficiency, Pregnant women}
  • مصطفی مجیدنیا*، آیلر کلته ای، احمد نورالدینی، حسن کوهی
    زمینه 

    کم خونی یکی از مهم ترین مشکلات در جهان است و به طور ویژه کودکان خردسال و زنان باردار را درگیر می کند.
    هدف مطالعه حاضر با هدف تعیین فراوانی آنمی دوران بارداری و عوامل مرتبط با آن انجام شد.

    روش ها

    این مطالعه مقطعی تحلیلی در سال 1399 با استفاده از اطلاعات زنان باردار تحت پوشش دانشگاه علوم پزشکی گلستان از سامانه ناب اجرا شد. افراد شرکت کننده شامل هزار نفر بودند که مراقبت های بارداری را در یکی از مراکز جامع سلامت دریافت و آزمایش های روتین بارداری را انجام داده بودند. جهت بررسی عوامل فردی-باروری مرتبط با کم خونی از آزمون های کای دو و رگرسیون لجستیک چندگانه استفاده شد.

    یافته ها 

    شیوع کم خونی در افراد تحت مطالعه 18/4 درصد بود که از این تعداد 19/27 درصد کم خونی شدید، 63/03 درصد کم خونی متوسط و 17/7 درصد کم خونی خفیف داشتند. این میزان با فاصله بین بارداری، رتبه زایمان، سن در اولین بارداری، سن ازدواج، ماه بارداری، سابقه ابتلا به عفونت دستگاه ادراری، تعداد مراقبت ها و تحصیلات رابطه معنی داری داشت (0/05> P). بین شیوع کم خونی دوران بارداری با محل سکونت و محل مراقبت زنان باردار رابطه ای مشاهده نشد.

    نتیجه گیری

    باتوجه به یافته ها، با افزایش ماه بارداری، داشتن سابقه عفونت ادراری، سن پایین ازدواج، کم بودن تعداد مراقبت های دریافتی در طول بارداری و پایین بودن سطح سواد شانس کم خونی دوران بارداری نیز افزایش می یابد. بنابراین شناسایی زنان در معرض خطر و اطمینان از مراقبت کافی و به موقع از آن ها مهم است.

    کلید واژگان: کم خونی, فقر آهن, بارداری, زایمان, زنان باردار}
    Mostafa Majidnia*, Aylar Kalteh Ei, Ahmad Nooreddini, Hasan Kohi
    Background 

    Anemia is one of the most important disorders in the world mostly affecting children and pregnant women.
    Objective This study aims to assess the prevalence of maternal anemia and its related factors among pregnant women in Golestan Province of Iran.

    Methods

    This cross-sectional analytical study was conducted on 1000 pregnant women referred to a comprehensive health center affiliated to Golestan University of Medical Sciences, Golestan, Iran in 2020. Chi-square (x2) and multiple logistic regression analysis were used to find demographic/obstetric factors related to maternal anemia.

    Results 

    The prevalence of anemia was 18.4%; 19.27% ​​had severe anemia, 63.03% had moderate anemia and 17.7% were with mild anemia. The interpregnancy interval, parity, age of first pregnancy, age of marriage, pregnancy month, history of urinary tract infection, number of medical care, and education had a significant relationship with maternal anemia (P<0.05), but the place of residence and the place to get medical care had no significant relationship with the maternal anemia.

    Conclusion 

    With increase in the pregnancy month, history of urinary tract infection, low age of marriage, low number of received medical care, and low educational level, the risk of maternal anemia increases. It is important to identify women at risk of anemia and ensure adequate and timely care for them.

    Keywords: Anemia, Iron deficiency, Pregnancy, Childbirth, Pregnant women}
  • Kien Nguyen Trung*, Hung Ta Viet, Hanh Nguyen Thi Hien, Van Nguyen Khanh, Tuyen Thai Danh, Thang Le Viet
    Background

    Iron management is essential for anemia treatment in chronic kidney disease. The reticulocyte hemoglobin equivalent (RET-He) is a reticulocyte parameter that reflects hemoglobin synthesis of newly formed erythrocytes in the bone marrow in real-time.

    Objectives

    This study aims to evaluate the role of reticulocyte hemoglobin equivalent (RET-He) in predicting iron deficiency in chronic kidney disease (CKD) patients.

    Methods

    Following a descriptive cross-sectional observational design, this study was conducted on 131 adult patients with CKD stages 3 - 5. Laboratory indices, including complete blood count, some biochemical indices, iron status, and reticulocyte indices (including RET-He), were measured. Iron deficiency (ID) was defined as TSAT < 20%, where serum ferritin level > 100 ng/mL was defined as functional ID, while serum ferritin level <100 ng/mL was defined as absolute ID.

    Results

    Nearly 42% of patients had ID. The mean concentration of RET-He in CKD patients with ID was significantly lower than that of patients without ID (P < 0.001). Based on the Receiver Operating Characteristic (ROC) curve model, RET-He had a good predictive value for ID in CKD patients (AUC = 0.762; P < 0.001; cut-off value: 28.15 g/L, the sensitivity of 45.5%, and the specificity of 100%). Serum iron, RET-He, serum albumin, and mean corpuscular volume (MCV) were independent risk factors to predict ID in CKD patients.

    Conclusions

    This study demonstrated that RET-He is an appropriate index to predict ID in CKD patients.

    Keywords: RET-He, Iron Deficiency, CKD}
  • Shima Jafari, Azita Talasaz*, Abbas Salehiomran, Hamid Ariannejad, Arash Jalali
    Background

    Preoperative anemia is an independent risk factor for higher rates of blood transfusion in cardiac surgery. This study aimed to evaluate the effects of intravenous iron sucrose and erythropoietin on transfusion requirements in patients with preoperative iron deficiency anemia (IDA) undergoing on-pump coronary artery bypass graft (CABG) surgery.

    Methods

    In this open-label, randomized clinical trial, patients with preoperative IDA who were candidates for on-pump CABG were randomized into intervention (iron plus erythropoietin) or control groups. Iron sucrose was administered as a 200 mg intravenous dose and erythropoietin as a 100 IU/kg bolus 1 to 2 days before surgery. The primary outcome was the amount of blood transfusion during the first 4 postoperative days.

    Results

    The study population consisted of 114 patients. The mean age was 64.11±8.18 years in the intervention group and 63.35±8.70 years in the control group. Twenty-seven patients (47.4%) in the intervention group and 25 (43.9%) in the control group were males. The number of red blood cell units transfused per patient exhibited a significant fall in the intervention group compared with the control group (P˂0.001). The ferritin level showed a significant rise in the intervention group on postoperative day 7 (P=0.027). The length of stay in the intensive care unit and the hospital was significantly lower in the intervention arm (P=0.041 and P=0.006, respectively). No adverse events were reported in both groups.

    Conclusion

    The use of erythropoietin and iron sucrose 1 to 2 days before surgery significantly decreased the need for blood transfusion in patients with IDA undergoing CABG without any significant adverse events.

    Keywords: Anemia, iron-deficiency, Blood transfusion, Coronary artery bypass, Erythropoietin}
  • Seyed Ahmad Rasoulinejad, Abolfazl Akbari*
    Background and Objective

    Retinopathy of premature (ROP) is known as the abnormal growth of retinal blood vessels in premature infants, occurring mainly due to the exposure to high levels of oxygen. Improper growth of retinal vessels because of ischemia-reperfusion causes oxidative damage and inflammation, and this condition is exacerbated by the abnormal proliferation of new vessels (neovascularization).

    Methods

    Zinc and iron, as the most abundant trace metals in the retina, control the redox-oxidation state in the retina; they also act as cofactors for many enzymes, including antioxidant enzymes. The deficiency of these two elements is common in preterm neonates and is considered one of the pathogens of ROP.

    Findings

    Adequate zinc and iron levels inhibited not only inhibit oxidative damage and inflammation caused by hypoxia but also vascular endothelial growth factor (VEGF) expression. In support of this mechanism, the results of the study showed that premature infants receiving high doses of zinc and adequate doses of iron significantly reduce the ROP process.

    Conclusion

    Oxidative damage and inflammation due to vascular ischemia in the retina are a major cause of ROP in infants, which may be due to zinc and iron deficiency. Therefore, monitoring serum zinc and iron levels and normalizing them may play an important preventive role in the development of retinopathy of prematurity.

    Keywords: Iron Deficiency, Zinc Deficiency, Retinopathy of Premature}
  • محمدعلی شعبان، اصغر قربانی، محمد کاجی یزدی*، ندا حکیمیان، منیر السادات سهل آبادی، زهرا شکری، زهرا ملا اسماعیلی
    زمینه و هدف

    آنمی میکروسیتیک فقر آهن شایع ترین اختلال تغذیه ای و از مشکلات بهداشتی عمده در نوزادان و کودکان است که با رشد و تکامل ناکافی آن ها همراه است. مطالعه حاضر با هدف تعیین شیوع آنمی میکروسیتیک در نورزادان در بدو تولد در بیمارستان بهارلو تهران انجام شد.

    روش بررسی

    تعداد 210 نوزادی که بین مهر ماه 1397 تا اسفند ماه سال 1397 در بیمارستان بهارلو تهران به دنیا آمده اند مورد بررسی قرار گرفتند. cc 5/2 خون بندناف از نوزادان تازه به دنیا آمده گرفته شد و سلول های خونی مورد بررسی قرار گرفت. با بررسی نتایج شاخص ها آنمی میکروسیتیک تشخیص داده شد و بررسی رابطه آنمی میکروسیتیک با شاخص هایی مانند اطلاعات دموگرافیک صورت گرفت.

    یافته ها: 

    میزان نوزادانی که مبتلا به آنمی هستند 3/14% و میزان نوزادانی که آنمی میکروسیتیک دارند 5/9% می باشند. ارتباط معناداری بین سطح غلظت هموگلوبین و آنمی میکروسیتیک نشان داده شد. ارتباطی بین سن مادر، وزن نوزادان، قد نوزادان، نوع زایمان، سن حاملگی و نسبت والدین با بروز آنمی میکروسیتیک مشاهده نشد.

    نتیجه گیری: 

    آنمی در مرکز بهارلو از شیوع نسبتا بالایی برخوردار است، بنابراین، امر غربالگری و بررسی بیشتر از نظر ابتلا به بیماری کم خونی و عوامل مرتبط با آن از اهمیت بسیار بالایی برخوردار است. نتایج مطالعات نشان گر آن است که آنمی یک بیماری چند فاکتوری می باشد و بروز آن به عوامل مختلف بستگی دارد و نیازمند غربالگری و تشخیص به موقع جهت بکارگیری درمان موثرتر و کاستن از عوارض احتمالی آن می باشد.

    کلید واژگان: آنمی, آنمی میکروسیتیک, نوزادان}
    MohammadAli Shaban, Asghar Ghorbani, Mohammad Kaji Yazdi*, Neda Hakimian, Monir Al Sadat Sahlabadi, Zahra Shokri, Zahra Mollah Esmaeili
    Background

    Anemia has a very high prevalence across the world. Microcytic anemia is the most common nutritional disorder and a major health problem in infants and children associated with inadequate growth and development. Diagnosing anemia at the birth can be difficult. Due to the fact that conditions such as thalassemia and iron deficiency are causative factors of microcytic anemia are prevalent in Iran, early diagnosing and treating these diseases can prevent excessive costs and further complications. Therefore, recognizing the practical factors with this complication is an effective step in controlling and preventing it. Therefore, the present study was performed to determine the prevalence of microcytic anemia in newborns in Baharloo Hospital in Tehran, Iran.

    Methods

    This cross-sectional study was performed on 210 infants, which were newly born on Baharloo Hospital from march2018 to march2019. 2.5 cc cord blood sample was extracted from each infant, and microcytic anemia were diagnosed according to factors such as Hb, MCV and others parameters.

    Results

    in this study, we demonstrated that there is a significant association between MCH and microcytic anemia. Our results showed that the rates of newborn infants with anemia disease (Hb<13ml/dl) were 14.3% and the rates of microcytic anemia were 9.5%. There were not any significant differences between motherchr('39')s age, neonatal weight and height, type of parturition, pregnancy age and parental ratio with the incidence of microcytic anemia.

    Conclusion

    Anemia has a relatively high prevalence in the center of Baharloo Hospital, Tehran, Iran. So screening and further investigation for anemia and related factors are critical. According to the results of our investigation, studies showed that anemia is a multifactorial disease that depends on different factors. The existence of variable results in different studies requires evaluating more parameters that affect the incidence of microcytic anemia, such as iron deficiency, eating habits, level of parental education, and use of iron supplements in pregnancy. Management of this disease requires screening and early diagnosis for more effective treatment and reduction of its potential complications.

    Keywords: anemia, iron deficiency, newborn}
  • Hossein Karami, Mohammad Naderisorki*, Maryam Ghasemi, Mobin Ghazaiean

    One of the most common nutritional deficiencies worldwide is iron deficiency. Fatigue, pallor, vertigo, dyspnea, cold intolerance, lethargy, palpitation, headache, and the pallor of the mucous membranes or nail beds are the most frequent symptoms and signs of iron deficiency. Thrombocytosis is commonly observed in iron deficiency anemia; it seems that erythropoietin plays the main role in this respect. Furthermore, thrombocytopenia and even leukopenia have been reported in iron deficiency; however, pancytopenia is a very rare condition. In this report, we presented two unusual cases of pancytopenia due to severe iron deficiency that improved after treatment with oral iron supplements. Iron deficiency anemia, if sufficiently severe, may be associated with reduced platelet and leukocyte counts. Accordingly, this condition should be considered as a differential diagnosis in all patients with pancytopenia.

    Keywords: Pancytopenia, Iron deficiency, Anemia}
  • Kourosh Goudarzipour, Hanieh Sadat Mirzadeh*, Mohammad Amin Shahrbaf, Saeed Sadr, Fatemeh Abdollah Gorji
    Background

    The prevalence of iron deficiency is increasing in the cystic fibrosis (CF) patients. The aim of this study was to determine the prevalence of iron deficiency ane-mia and its correlation with pulmonary function in cystic fibrosis patients.

    Materials and Methods

    This descriptive-analytic study was conducted on the patients with cystic fibrosis who were referred to the Mofid Children Hospital, Tehran, Iran during 2015-2016. Complete blood counting and iron indices were evaluated; furthermore, Pulmonary function test was performed in ≥ 5 years old patients to determine the forced expiratory volume in first second (FEV1), forced vital capacity (FVC), FEV1/FVC and forced expiratory flow (FEF25-75). The data were analyzed by SPSS software. Pear-son correlation coefficient, t-test, Fisher’s exact test and χ2 were used for analyzing data.

    Results

    Among 62 CF patients who presented to the hospital in the study period, 30 patients were able to perform spirometry and included in the study. Spirometry findings were normal in 12 patients (40%) which 72% of them were female. There was a sta-tistically significant correlation between the spirometric findings and the gender of the patients (P < 0.05); although, the correlation between the gender and iron indices was not significant (P > 0.05). Moreover, there was no statistically significant correlation between spirometric findings and iron indices (P > 0.05).

    Conclusion

    There was no significant correlation between the iron deficiency and the pulmonary function in cystic fibrosis patients.

    Keywords: Cystic fibrosis, Iron deficiency, Pulmo-nary function}
  • Fatemeh Haidari*, Behnaz Abiri, Mohammad‑Hossein Haghighizadeh, Gholam A. Kayedani, Negar K. Birgani
    Background

    Iron deficiency is prevalent in overweight and obese individuals and may be induced by adiposity‑related inflammation that affect iron metabolism.

    Objective

    The objective of this study was to investigate the relationship between hematological parameters and obesity‑induced inflammation among young females.

    Methods

    A total of 170 young women (aged between 18‑35 years) participated in this cross‑sectional study. Obesity was assessed by BMI (body mass index), WHR (waist to hip ratio), and body fat percentage. Inflammatory and hematological parameters including hs‑CRP (high‑sensitivity C‑reactive protein), serum Fe, hemoglobin, ferritin, transferrin, TIBC (total iron binding capacity) were measured. Dietary intakes of some nutrients (total iron, proteins, calcium, and vitamin C) were assessed according to BMI, WHR and fat mass categories.

    Results

    Serum iron were negatively correlated with BMI (P = 0.045, r = −0.154) and hs‑CRP (P = 0.032, r = −0.165). Hemoglobin were also negatively correlated with BMI (P = 0.043, r = −0.155). A significant correlation was also shown between WHR with transferrin (P = 0.034, r = 0.163) and TIBC levels (P = 0.035, r = 0.162), hs‑CRP was positively correlated with BMI (P = 0.014, r = 0.183), WHR (P = 0.009, r = 0.202) and body fat percentage (P = 0.037, r = 0.353). Dietary intakes did not differ significantly among BMI, WHR and fat mass categories (P > 0.05).

    Conclusions

    Obesity‑induced inflammation, regardless of dietary intake of iron, can lead to iron deficiency. Therefore, weight control, especially in obese subjects is necessary to prevent iron deficiency and anemia.

    Keywords: Hematological parameters, inflammation, iron deficiency, obesity, young female}
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