Publications by authors named "Daghestani M"

Article Synopsis
  • Oral contraceptives (OCs) are commonly used by women for pregnancy control and health issues, but misconceptions about their benefits and risks exist.
  • A study in western Saudi Arabia surveyed women aged 15-49 using an online questionnaire to assess their awareness of OCs.
  • Results showed only 13.6% of participants had excellent knowledge, with most information coming from friends/relatives and physicians, highlighting a connection between reliable sources and knowledge levels.
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This study investigates the phytoremediation potential of non-productive seedlings of Ailanthus altissima, Acer pseudoplatanus, and Fraxinus excelsior for lead, cadmium, and zinc accumulation in contaminated soils of Zanjan Province, an industrial area with significant pollution. The evaluation employed a completely randomized design, with three treatment levels for each element, alongside a control treatment, replicated three times over a two-year period. A total of 810 one-year-old seedlings from the three species were involved in the study.

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  • BTBGD is a rare genetic disorder caused by mutations in the SLC19A3 gene, leading to severe neurological symptoms like confusion, seizures, and disabilities.
  • Diagnosis is challenging due to the disease's rarity and varied symptoms, with current treatment involving thiamine and biotin supplementation, although long-term effectiveness is still unclear.
  • Researchers have created induced pluripotent stem cell (iPSC) lines from a BTBGD patient, which can help study the disease's mechanisms and potentially lead to new treatments.
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The objective of this case report is to discuss a case of septicemia caused by following cervical cerclage. The study described a case of a 42-year-old female patient who visited the Ante-natal Clinic for a follow-up appointment during the 8th week of gestation. The patient had previously undergone successful in vitro fertilization treatment following 16 years of primary infertility.

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Decorin (DCN), a member of the small leucine-rich proteoglycan gene family, is secreted from stromal fibroblasts with non-cell-autonomous anti-breast-cancer effects. Therefore, in the present study, we sought to elucidate the function of decorin in breast stromal fibroblasts (BSFs). We first showed DCN downregulation in active cancer-associated fibroblasts (CAFs) compared to their adjacent tumor counterpart fibroblasts at both the mRNA and protein levels.

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Background: Human iPSCs' derivation and use in clinical studies are transforming medicine. Yet, there is a high cost and long waiting time associated with autologous iPS-based cellular therapy, and the genetic engineering of hypo-immunogenic iPS cell lines is hampered with numerous hurdles. Therefore, it is increasingly interesting to create cell stocks based on HLA haplotype distribution in a given population.

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Article Synopsis
  • Dravet syndrome (DRVT) is a common epileptic encephalopathy primarily linked to SCN1A gene mutations in 80% of cases.
  • Researchers have created induced pluripotent stem cells (iPSCs) to model DRVT, but no studies have focused on rare genetic variants until now.
  • This study introduces two new DRVT-iPSC lines with specific mutations in CPLX1 and SCN9A, offering a valuable tool to explore the molecular mechanisms behind the associated cellular dysfunctions.
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Objectives: To determine the allelic frequencies and effects of genotypic variations in cytokine gene polymorphisms in a Saudi Arabian population.

Methods: This cross-sectional study involved 41 patients with Primary Sjögren's syndrome (pSS) and 71 healthy controls between October 2018 and May 2019. Single nucleotide polymorphisms genotyping was performed using the SEQUENOM MassARRAY System, targeting nine polymorphisms in different cytokine genes.

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Article Synopsis
  • Primary Sjögren's syndrome (pSS) is an autoimmune disorder linked to fatigue and various extraglandular manifestations, resulting from dysregulated cytokine networks that affect exocrine glands.* -
  • The study involved 41 pSS patients and 71 control subjects from King Saud University Medical City, measuring serum cytokines and assessing their correlation with disease activity (via ESSDAI), extraglandular manifestations (EGMs), and fatigue levels.* -
  • Key findings showed that many patients had EGMs, significant differences in cytokine levels (e.g., lower TNFα and IL-21, higher IL-12 in pSS), and varying cytokine levels associated with disease activity and fatigue, with
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Rheumatoid arthritis (RA) is an autoimmune inflammatory disease that causes multi-articular synovitis. The illness is characterized by worsening inflammatory synovitis, which causes joint swelling and pain. Synovitis erodes articular cartilage and marginal bone, resulting in joint deterioration.

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Unlabelled: Rheumatoid arthritis (RA) is a complex, multifactorial disorder with an autoimmune etiology. RA is highly heritable and is associated with both human leucocyte antigen (HLA) and non-HLA genes. We investigated the associations of 33 single nucleotide polymorphisms (SNPs) with RA in the Saudi population.

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Myoglobin (MB) is a cytoplasmic hemoprotein that is predominantly expressed in the heart and oxidative myofibers of skeletal muscle. It has been demonstrated that MB binds to oxygen and promotes its diffusion for energy production in the mitochondria. Recently, MB was found to be expressed in different forms of malignant tumors and cancer cell lines.

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Objectives: To determine the prevalence of selected single nucleotide polymorphisms (rs1080985, rs28624811, rs1065852, rs28371725, and rs1135840) in () gene among Saudi systemic lupus erythematosus (SLE) patients and to investigate the association between the genetic variants and clinical features of SLE.

Methods: This cross-sectional study was carried out on adult Saudi patients at King Khalid University Hospital, Riyadh, Saudi Arabia. Patients with confirmed SLE based on the 2012 Systemic Lupus International Collaborating Clinics classification criteria were included in the study.

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Compound heterozygous mutations in SHQ1 have been associated with a rare and severe neurological disorder characterized by global developmental delay (GDD), cerebellar degeneration coupled with seizures, and early-onset dystonia. Currently, only five affected individuals have been documented in the literature. Here, we report three children from two unrelated families harboring a homozygous variant in the gene but with a milder phenotype than previously described.

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Article Synopsis
  • Ovarian hyperstimulation syndrome (OHSS) is a complication often linked with polycystic ovarian syndrome (PCOS), a common endocrine disorder in women during their reproductive years.
  • Researchers analyzed the RNA from granulosa cells of PCOS patients, comparing those with a history of OHSS to those without, and discovered 59 genes that were significantly altered, indicating differences in cellular processes and inflammation related to OHSS.
  • This study represents the largest analysis of Saudi PCOS cases using transcriptomic methods, highlighting important gene networks and pathways associated with the condition, suggesting a need for further research to validate these findings.
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Increasing numbers of patients who recover from COVID-19 report lasting symptoms, such as fatigue, muscle weakness, dementia, and insomnia, known collectively as post-acute COVID syndrome or long COVID. These lasting symptoms have been examined in different studies and found to influence multiple organs, sometimes resulting in life-threating conditions. In this review, these symptoms are discussed in connection to the COVID-19 and long-COVID-19 immune changes, highlighting oral and psychiatric health, as this work focuses on the gut microbiota's link to long-COVID-19 manifestations in the liver, heart, kidney, brain, and spleen.

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Objectives: Obstetrical hemorrhage contributes significantly to maternal morbidity and mortality. Assessment of blood loss while undergoing cesarean sections (CS) is essential in lowering the morbidity and mortality, however this amount is commonly underestimated by the surgeon and probably the anesthetist too.

Methods: This study addresses this issue by comparing three separate ways of assessing blood loss during cesarean sections.

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Purpose: The COVID-19 pandemic might add to the stressors experienced by people living with rheumatic diseases. This study aimed to examine rheumatic patients' functional and psychosocial states during the pandemic and assess its impact on their quality of life.

Methods: Our time-series study included a patient-centered electronic survey, sampling adult rheumatic patients living in Saudi Arabia at different time points from March to August 2020.

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The role of inflammation in colon cancer is understood as a well-accepted factor that has the tendency to release multiple pro- and anti-tumorigenic inflammatory mediators. Inflammation-induced increased expression of anti-tumorigenic inflammatory mediators and decreased expression of pro-tumorigenic inflammatory mediators encourage beneficial inflammatory effects in terms of powerful anti-tumor immunity. The present study aims to screen the beneficial inflammatory effects of venom via determining its modulatory tendency on the expression of 40 pro- and anti-tumorigenic inflammatory mediators (cytokines/growth factors/chemokines) in LoVo human colon cancer cell line.

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Colorectal cancer (CRC) is a disease with high incidence worldwide. As of 2018, it is the second leading cause of cancer deaths in the world. In Saudi Arabia, the incidence of this disease has been increasing in the younger population.

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In this study we isolated and enriched erythroid progenitor cells (EPCs) from a 10 ml peripheral blood sample from a 37-year old healthy Saudi donor. After expansion, these EPCs were reprogrammed using episomal plasmids to generate an induced pluripotent stem (iPS) cell line, KAIMRCi001-A. The pluripotency of this line was confirmed by measuring the expression of typical pluripotency markers and assessing differentiation potential in vitro.

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Systemic Lupus erythematosus (SLE) is a chronic multisystem, multifactorial inflammatory autoimmune disease. The SLE patients have 3 times increased risk of mortality based on international data with ethnicity playing an important impact on patients' morbidity and mortality. Descriptive studies from Saudi Arabia showed variation in clinical features from one region to another.

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The aim of the present study, is to investigate the influence of obesity, with and without polycystic ovarian syndrome (PCOS), on the levels of kisspeptin, vitamin D (Vit D), and vascular endothelial growth factor (VEGF) and to explore the relationship between these parameters and endocrine and metabolic variables. The study group included 126 obese Saudi females. Of these 63 were suffering from PCOS while the rest were normo-ovulatory obese women (non-PCOS obese).

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Objectives: To describe primary Sjögren's syndrome (pSS) cohort in Saudi Arabiain view in of clinical/serological/histopathological phentotype, and, diagnostic delay.

Methods: A cross-sectional study conducted between October 2018 and May 2019. Diagnostic delay was calculated from symptoms onset to clinical diagnosis.

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Background: Polycystic ovarian syndrome (PCOS) is a frequently encountered disorder. This study aimed to identify polymorphisms in ADRB2 in Saudi PCOS development and to study its influence on lipids, hormones, and anthropometric parameters.

Methods: Saudi females (100) suffering from PCOS and healthy controls (100) were investigated.

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