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British Journal of Medical and Health Research

📢 Latest Update: Call for Papers: Special Issue on Medical and Health Research – Submit to British Journal (BJMHR) by March 31, 2026

📢 Latest Update: Call for Papers: Special Issue on Medical and Health Research – Submit to British Journal (BJMHR) by March 31, 2026

Volume 10, Issue 2 - 2023 (February 2023 Issue 2)

Volume 10 Issue 2 Cover

Issue Details:

Volume 10 Issue 2
Published:Invalid Date

Editorial: February 2023 Issue 2

Welcome to the 2023 issue of British Journal of Medical and Health Research. This issue showcases the remarkable breadth and depth of contemporary research across multiple disciplines. From cutting-edge applications of machine learning in climate science to the revolutionary potential of quantum computing in drug discovery, our featured articles demonstrate the power of interdisciplinary collaboration in addressing global challenges.

We are particularly excited to present research that bridges traditional academic boundaries, reflecting our journal's commitment to fostering innovation through cross-disciplinary dialogue. The integration of artificial intelligence with environmental science, the application of blockchain technology to supply chain management, and the convergence of urban planning with smart city technologies exemplify the transformative potential of collaborative research.

As we continue to navigate an era of rapid technological advancement and global challenges, the research presented in this issue offers both insights and solutions that will shape our future. We thank our authors, reviewers, and editorial board members for their continued dedication to advancing knowledge and promoting scientific excellence.

Dr Hemangi J Patel
Editor-in-Chief
British Journal of Medical and Health Research

Articles in This Issue

Showing 4 of 4 articles
Research PaperID: BJMHR1002001

Heterogeneity Of Renal Pathogenicity On The Background Of Asymptomatic Hyperuricemia In Patients With Dual Metabolic Syndrome Diseases (Essential Hypertensive Disease and Type 2 Diabetes Mellitus)

Aloysius Obinna Ikwuka, N. G. Virstyuk, O.R. Luchko, I. Kobitovych

ABSTRACT Asymptomatic hyperuricemia is believed to be more severe and more common in patients with dual metabolic syndrome diseases (essential hypertensive disease (EHD) and type 2 diabetes mellitus (T2DM)) and comparatively less severe and less common in patients with either of these dual metabolic syndrome diseases. To determine the heterogeneity of renal pathogenicity on the background of asymptomatic hyperuricemia in the clinical course of EHD combined with T2DM using correlations between uric acid levels in the blood, systolic blood pressure levels, glycated hemoglobin, dyslipidemia, inflammatory processes, kidney damage, etc. The research included 105 patients (50 males and 55 females), aged 41-70 years, average age being (54.2±4.0) years. Patients were divided into 3 groups: Group I (GI) consisted of 25 patients with treatment-compensated EHD, 1-2 degree, stage II; Group ІІ (GII) was made up of 25 patients with subcompensated T2DM (glycated hemoglobin (HbA1C) - from 7.0 to 11.0%); Group III (GIII) had 55 patients with EHD, 1-2 degree, stage ІІ combined with subcompensated T2DM. Control group consisted of 15 practically healthy volunteers, 10 (66.7%) females and 5 (33.3%) males, aged (54.6±4.2) years. Groups were randomized according to age, sex, BMI, duration of EHD and T2DM. In addition to general clinical examination conducted; blood levels of uric acid (UA), lipids, tumour necrosis factor alpha (TNF-α), high-sensitivity C-reactive protein (hs-CRP) were determined. Urine levels of neutrophil gelatinase-associated lipocalin (NGAL) was also determined using immuno-fermentation methods. Asymptomatic hyperuricemia characterized by an increase in blood uric acid level of more than 410 μmol/l was observed in 34.6% of GI patients, in 21.8% of GII patients and most commonly in 55.7% of GIII patients with EHD combined with T2DM. Correlations between blood uric acid level with albuminuria was found (r=+0.42; p<0.05); with decrease in GFR (r=-0.51; p<0.05); with increase in NGAL level in urine (r=+0.56; p<0.05), which indicate an adverse effect of asymptomatic hyperuricemia on the functional state of the kidneys in patients with EHD and concomitant T2DM. Positive correlative relationships exist between asymptomatic hyperuricemia, increased albuminuria and a decrease in GFR, dyslipidemia, SBP, HbA1C, inflammatory processes and kidney damage, which indicate the heterogeneity of renal pathogenicity in patients with EHD combined with T2DM and a higher risk of cardiovascular disease in such patients. Keywords: Heterogeneity, renal pathogenicity, asymptomatic hyperuricemia, metabolic syndrome diseases, essential hypertensive disease, type 2 diabetes mellitus

Heterogeneityrenal pathogenicityasymptomatic hyperuricemiametabolic syndrome diseasesessential hypertensive diseasetype 2 diabetes mellitus
53,471 views
16,177 downloads

Contributors:

 Aloysius Obinna Ikwuka
,
 N. G. Virstyuk
,
 O.R. Luchko
,
 I. Kobitovych
Research PaperID: BJMHR1002002

A RARE CASE REPORT: COLPOCEPHALY AS A CAUSE OF STATUS EPILEPTICUS

Param Dhami, Darshana Makwana, Dipenkumar Patel, Umesh Kanzariya

Colpocephaly is a rare congenital brain malformation resulting in disproportionately large occipital horns of lateral ventricles compared to frontal ones resulting from corpus callosal and other white matter developmental arrest. Colpocephaly can be associated with partial or complete agenesis of the corpus callosum, chiari malformations, lissencephaly, and microcephaly. Colpocephaly can present with headache, seizure disorder, visual impairment, movement abnormalities and muscle spasms or can even be asymptomatic. We report a case of a 21-year old male with colpocephaly presenting as a status epilepticus (SE) as an initial symptom along with incidental cardiac anomaly OS ASD (Ostium secundum atrial septal defect) found on routine screening.

ColpocephalyStatus EpilepticusOstium Secondum Atrial Septal DefectVentriculomegalyCorpus callosal agenesis
53,881 views
16,158 downloads

Contributors:

 Param Dhami
,
 Darshana Makwana
,
 Dipenkumar Patel
,
 Umesh Kanzariya
Research PaperID: BJMHR1002003

COMPLETELY EDENTULOUS PATIENTS SCREW-RETAINED MAXILLARY COMPLETE DENTURE WITH ELECTRIC WELDED METAL FRAMEWORK VERSUS CAST ONE, PATIENT SATISFACTION ASSESSMENT.

fatma hussein abd elmonem, nora mohamed sheta, doaa amr rostom

Aim: To evaluate patient satisfaction of electrically welded and cast metal frameworks in the screw-retained implant-supported prosthesis. Methodology: 12 completely edentulous patients received complete dentures; six implants were inserted in maxillary arch. Second-stage surgery was performed following the usual protocol. Shaping abutments were connected to the implants on one side of the arch, and titanium wire was bent and attached to the implants by intraoral electric welding. On the other side, the cast metal framework was performed. Then both cast and welded frameworks were picked up in the complete maxillary denture after their modification. Patient satisfaction was assessed within 2 weeks, 4 months, 6 months, and 12 months after prosthesis delivery. Results: Throughout the intervals, there was a significant increase in patient satisfaction with the prosthesis, but there was no significant difference between the two groups. Conclusions: The intra-oral electric welding is considered a promising treatment option compared to the conventional cast framework regarding patient satisfaction when used under screw-retained implant-supported prosthesis.

complete dentureelectric welded frameworkscrew retained prosthesis.
53,959 views
16,286 downloads

Contributors:

 fatma hussein abd elmonem
,
 nora mohamed sheta
,
 doaa amr rostom
Research PaperID: BJMHR1002004

Leucocyte Adhesion Deficiency-1 Presenting as Leukocytosis and Pyoderma Gangrenosum

Dr. Steffi Thomas, Dr. Nilesh Wasekar

Leukocyte Adhesion Disorder is a rare autosomal recessive disorder characterized by immunodeficiency caused by compromised neutrophil adhesion and transmigration activity to inflammation sites resulting in recurrent infections, of which Type 1 is the most common. We are herewith reporting an interesting case of a 17 year old female patient who presented with skin lesions over lower limb for 15-30 days which on further investigating found out to be Pyoderma Gangrenosum in a case of LAD type 1. Patient was managed with antibiotics, steroids, hydration and supportive care. The lesion responded to steroids and completely vanished with some residual scarring in 3-4months time. Early diagnosis and appropriate line of treatment with oral as well as injectable steroids and antibiotics helped us in combating this rare disease.

Leukocyte Adhesion DisorderLAD Type 1Pyoderma GangrenosumCD18CD34
54,005 views
16,154 downloads

Contributors:

 Dr. Steffi Thomas
,
 Dr. Nilesh Wasekar