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1.
J Med Screen ; 30(4): 161-167, 2023 12.
Article in English | MEDLINE | ID: mdl-37066693

ABSTRACT

OBJECTIVES: Hemoglobinopathies are the commonest inherited blood disorders and form a serious burden worldwide, affecting communities, patient quality of life and healthcare resources. The Kingdom of Bahrain has issued a law obligating couples to undergo premarital screening to detect those at risk of having children affected with these disorders. The aim of this study was to analyze the marital decisions of couples at risk for hemoglobinopathies and follow up the outcomes. METHODS: A retrospective study was conducted on couples at risk for hemoglobinopathies identified during the premarital screening program at local health centers in the Kingdom of Bahrain and referred to the genetics department in the Salmaniya Medical Complex for genetic counselling in 2018-2020. RESULTS: A total of 189 couples were found to be at risk for hemoglobinopathies, of whom 159 completed the survey. Of these, 107 (67%) decided to proceed with their marriage and 26 couples achieved pregnancy. Out of 24 at-risk pregnancies with known outcome, 83.3% were spontaneous whereas only 16.7% underwent in-vitro fertilization (IVF) with preimplantation genetic diagnosis (PGD). Eight out of 20 infants born to couples after spontaneous conception were affected. A positive attitude toward IVF with PGD was held by 60% of at-risk couples. CONCLUSIONS: Despite undergoing premarital screening and genetic counselling, a large percentage of at-risk couples proceeded with their marriage. Most of them justified their decision due to the availability of advanced methods that aid in the prevention of having an affected child. However, the cost of such intervention was a major barrier for the majority of couples.


Subject(s)
Genetic Counseling , Hemoglobinopathies , Pregnancy , Female , Child , Humans , Genetic Counseling/methods , Retrospective Studies , Bahrain , Quality of Life , Early Detection of Cancer , Hemoglobinopathies/diagnosis , Hemoglobinopathies/genetics , Genetic Testing , Premarital Examinations/methods , Premarital Examinations/psychology
2.
Sci Rep ; 11(1): 22199, 2021 11 12.
Article in English | MEDLINE | ID: mdl-34772994

ABSTRACT

Sickle cell disease, a common genetic blood disorder, results from a point mutation in the ß-globin gene affecting the configuration of hemoglobin, predisposing to painful vaso-occlusive crisis (VOC) and multi-organ dysfunctions. There is a huge variation in the phenotypic expressions of SCD and VOC owing to genetic and environmental factors. This study aimed to characterize the whole blood gene expression profile using Microarray technology in Bahraini patients with SCD determining the differentially expressed genes in steady-state (n = 10) and during VOC (n = 10) in comparison to healthy controls (n = 8). Additionally, the study intended to identify potential genetic marker associated with hemolysis. The analysis identified 2073 and 3363 genes that were dysregulated during steady-state and VOC, respectively, compared to healthy controls. Moreover, 1078 genes were differentially expressed during VOC compared to steady state. The PLSCR4 gene was almost 6-fold up-regulated in microarray, 4-fold in polymerase chain reaction, and a mean protein concentration of 0.856 ng/ml was observed in enzyme-linked immunosorbent assay during VOC compared to steady-state (0.238 ng/ml) (p < 0.01). Amongst these genes, PLSCR4 is involved in erythrocyte membrane deformity thus, predisposing to hemolysis, adhesion, and thrombosis. In conclusion, PLSCR4 may serve as a potential biomarker for VOC and future large-scale validation are recommended.


Subject(s)
Anemia, Sickle Cell/complications , Anemia, Sickle Cell/genetics , Biomarkers , Disease Susceptibility , Pain/etiology , Phospholipid Transfer Proteins/genetics , Adult , Anemia, Sickle Cell/blood , Anemia, Sickle Cell/diagnosis , Erythrocyte Indices , Female , Gene Expression , Gene Expression Profiling , Gene Expression Regulation , Humans , Male , Pain/diagnosis , Phospholipid Transfer Proteins/blood , Reproducibility of Results , Transcriptome , Young Adult
3.
Anesth Prog ; 57(3): 91-5, 2010.
Article in English | MEDLINE | ID: mdl-20843223

ABSTRACT

The objective of this study was to examine the public health relevance of the prevalence of dental fear in Kuwait and the resultant barrier that it creates regarding access to dental care. The study analysis demonstrated a high prevalence of dental fear and anxiety in the Kuwaiti population and a perceived need for anesthesia services by dental care providers. The telephone survey of the general population showed nearly 35% of respondents reported being somewhat nervous, very nervous, or terrified about going to the dentist. In addition, about 36% of the population postponed their dental treatment because of fear. Respondents showed a preference to receive sedation and anesthesia services as a means of anxiety relief, and they were willing to go to the dentist more often when such services were available. People with high fear and anxiety preferred to receive some type of medication to relieve their anxiety. In conclusion, the significance and importance of the need for anesthesia services to enhance the public health of dental patients in Kuwait has been demonstrated, and improvements are needed in anesthesia and sedation training of Kuwaiti dental care providers.


Subject(s)
Anesthesia, Dental , Conscious Sedation , Dental Anxiety/epidemiology , Dental Care/statistics & numerical data , Needs Assessment , Anesthesiology/education , Dentists/statistics & numerical data , Educational Status , Female , Humans , Interviews as Topic , Kuwait/epidemiology , Male , Prevalence , Prospective Studies , Surveys and Questionnaires
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