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1.
Cureus ; 15(9): e45719, 2023 Sep.
Article in English | MEDLINE | ID: mdl-37868488

ABSTRACT

Heart failure with reduced ejection fraction (HFrEF) is a clinical syndrome whose management has significantly evolved based on the pathophysiology and disease process. It is widely prevalent, has a relatively high mortality rate, and is comparatively more common in men than women. In HFrEF, the series of maladaptive processes that occur lead to an inability of the muscle of the left ventricle to pump blood efficiently and effectively, causing cardiac dysfunction. The neurohormonal and hemodynamic adaptations play a significant role in the advancement of the disease and are critical to guiding the treatment and management of HFrEF. The first-line therapy, which includes loop diuretics, ß-blockers, angiotensin-converting enzyme inhibitors/angiotensin II receptor blockers, hydralazine/isosorbide-dinitrate, and mineralocorticoid receptor antagonists (MRAs), has been proven to provide symptomatic relief and decrease mortality and complications. The newly recommended drugs for guideline-based therapy, angiotensin receptor/neprilysin inhibitor (ARNI), sodium-glucose cotransporter 2 inhibitors, soluble guanylate cyclase, and myosin activators and modulators have also been shown to improve cardiac function, reverse cardiac remodeling, and reduce mortality rates. Recent studies have demonstrated that exercise-based therapy has resulted in an improved quality of life, exercise capacity, cardiac function, and decreased hospital readmission rates, but it has not had a considerable reduction in mortality rates. Combining multiple therapies alongside holistic advances such as exercise therapy may provide synergistic benefits, ultimately leading to improved outcomes for patients with HFrEF. Although first-line treatment, novel pharmacologic management, and exercise-based therapy have been shown to improve prognosis, the existing literature suggests a need for further studies evaluating the long-term effects of MRA and ARNI.

2.
J Med Genet ; 55(7): 479-488, 2018 07.
Article in English | MEDLINE | ID: mdl-29572253

ABSTRACT

BACKGROUND: Usher syndrome (USH) is a neurosensory disorder characterised by deafness, variable vestibular areflexia and vision loss. The aim of the study was to identify the genetic defect in a Pakistani family (PKDF1051) segregating USH. METHODS: Genome-wide linkage analysis was performed by using an Illumina linkage array followed by Sanger and exome sequencing. Heterologous cells and mouse organ of Corti explant-based transfection assays were used for functional evaluations. Detailed clinical evaluations were performed to characterise the USH phenotype. RESULTS: Through homozygosity mapping, we genetically linked the USH phenotype segregating in family PKDF1051 to markers on chromosome 1p36.32-p36.22. The locus was designated USH1M. Using a combination of Sanger sequencing and exome sequencing, we identified a novel homozygous 18 base pair inframe deletion in ESPN. Variants of ESPN, encoding the actin-bundling protein espin, have been previously associated with deafness and vestibular areflexia in humans with no apparent visual deficits. Our functional studies in heterologous cells and in mouse organ of Corti explant cultures revealed that the six deleted residues in affected individuals of family PKDF1051 are essential for the actin bundling function of espin demonstrated by ultracentrifugation actin binding and bundling assays. Funduscopic examination of the affected individuals of family PKDF1051 revealed irregular retinal contour, temporal flecks and disc pallor in both eyes. ERG revealed diminished rod photoreceptor function among affected individuals. CONCLUSION: Our study uncovers an additional USH gene, assigns the USH1 phenotype to a variant of ESPN and provides a 12th molecular component to the USH proteome.


Subject(s)
Benign Paroxysmal Positional Vertigo/genetics , Deafness/genetics , Microfilament Proteins/genetics , Vision Disorders/genetics , Adult , Animals , Benign Paroxysmal Positional Vertigo/physiopathology , Deafness/physiopathology , Genetic Linkage/genetics , Genetic Predisposition to Disease , Genotype , Homozygote , Humans , Mice , Mutation , Pedigree , Phenotype , Retina/metabolism , Retina/physiopathology , Sequence Deletion/genetics , Vision Disorders/physiopathology , Exome Sequencing , Young Adult
4.
Anc Sci Life ; 8(3-4): 196-206, 1989 Jan.
Article in English | MEDLINE | ID: mdl-22557650

ABSTRACT

In this paper 180 cases of Anyedyushka and Thriteeyaka Vishamajwaras (P.vivax malaria) were studied for various biochemical changes before and after treatment and these changes were correlated with dosha-dushya involvement in these conditions. Their diagnostic, prognostic and therapeutic utility has also been discussed here.

6.
Anc Sci Life ; 2(2): 79-83, 1982 Oct.
Article in English | MEDLINE | ID: mdl-22556958

ABSTRACT

In this paper the contraceptive effect of Ayush AC-4 an ayurvedic compound preparation is assessed. Totally 281 volunteers have been enrolled in the study. Tho menstrual cycles covered by the women ranged from 1-30. Tho result is moderately satisfactory. No toxic symptoms or severe aide-effects were noticed. The authors say that in tho light of the results obtained in this study, it may be desirable and feasible to make this compound preparation acceptablo like the other oral contraceptives.

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