middle eastern population
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2022 ◽  
pp. 341-358

Episcleritis and scleritis are the most common diseases among disorders of sclera. Episcleritis is a relatively common condition in the Middle Eastern population. The true incidence is difficult to determine, as episcleritis are self-limited conditions and patients generally do not seek professional advice. Scleritis is characterized by a chronic inflammatory response located in the sclera, which can spillover and involve adjacent ocular structures, mainly the cornea and the uvea. Scleritis can be seen at any age, but most commonly occurs in the fourth to sixth decades. It has a small female preponderance (1.6:1), and the condition is bilateral in 52% of cases. This chapter includes a severe infectious scleritis case with before and after treatment photos. The disease responded to antibiotic treatment, but later the patient presented with immune disease recurrence which responded to oral immunosuppressive treatment. Treatment photos are shown chronologically.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Neyla S. Al Akl ◽  
Olfa Khalifa ◽  
Khaoula Errafii ◽  
Abdelilah Arredouani

AbstractElevated serum ferritin (SFer) levels are implicated in many energy metabolism abnormalities. The association between SFer levels and metabolic disorders has not been studied in Middle Eastern populations. We aimed at exploring the association between SFer levels and serum lipids, diabetes determinants, and metabolic syndrome in a sample of Qatari adults. This study used biochemical parameters obtained from 1928 participants from the Qatar Biobank cohort. We utilized adjusted multivariable logistic regression analysis to estimate the odds ratios (ORs) for dyslipidemia, type 2 diabetes, the homeostasis model assessment of insulin resistance (HOMA-IR), and metabolic syndrome (MetS) according to sex-specific SFer quartiles (Q1 to Q4). Results revealed that the ORs for dyslipidemia increased progressively and significantly across the SFer quartiles, up to two folds in Q4 for women (OR 2.47 (1.68–3.62)) and men (OR 2.24 (1.41–3.55)) versus Q1 (OR:1). Exclusively in women, the ORs for IR (HOMA-IR > 3.58) increased significantly in Q4 (OR 1.79 (1.19–2.70)) versus OR 1 in Q1 as did the ORs for diabetes (OR: 2.03 (1.15–3.57) in Q4 versus OR 1 in Q1). We observed the same result when we pooled the participants with prediabetes and diabetes in one group. The OR for MetS also increased significantly across the Sfer Quartiles from OR: 1 in Q1 to 1.92 (1.06–3.02) in Q4 for women and to 2.07 (1.08–3.98) in Q4 in men. Our results suggest the elevated Sfer levels as a potential risk biomarker for dyslipidemia and MetS in adult Qatari men and women, and diabetes and IR in women only.


2021 ◽  
Vol 141 (10) ◽  
pp. S161
Author(s):  
S. Bergson ◽  
D. Daniely ◽  
D. Bomze ◽  
T. Falik-Zaccai ◽  
E. Avitan-Hersh ◽  
...  

Author(s):  
Hamdi Mbarek ◽  
Geethanjali Devadoss Gandhi ◽  
Senthil Selvaraj ◽  
Wadha Al-Muftah ◽  
Radja Badji ◽  
...  

AbstractDespite recent biomedical breakthroughs and large genomic studies growing momentum, the Middle Eastern population, home to over 400 million people, is under-represented in the human genome variation databases. Here we describe insights from phase 1 of the Qatar Genome Program which whole genome sequenced 6,045 individuals from Qatar. We identified more than 88 million variants of which 24 million are novel and 23 million are singletons. Consistent with the high consanguinity and founder effects in the region, we found that several rare deleterious variants were more common in the Qatari population while others seem to provide protection against diseases and have shaped the genetic architecture of adaptive phenotypes. Insights into the genetic structure of the Qatari population revealed five non-admixed subgroups. Based on sequence data, we also reported the heritability and genetic marker associations for 45 clinical traits. These results highlight the value of our data as a resource to advance genetic studies in the Arab and neighbouring Middle Eastern populations and will significantly boost the current efforts to improve our understanding of global patterns of human variations, human history and genetic contributions to health and diseases in diverse populations.


2021 ◽  
Vol 22 (4) ◽  
pp. 279-283
Author(s):  
Irfan Shafiq ◽  
◽  
Safia Shabeer ◽  
Mateen Haider Uzbeck ◽  
Zaid Zoumot ◽  
...  

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