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1.
J Neurosurg Sci ; 58(3): 177-82, 2014 Sep.
Article in English | MEDLINE | ID: mdl-25033977

ABSTRACT

AIM: A common cause of low back pain is lumbar spinal stenosis (LSS). The Swiss Spinal Stenosis Score (SSS) is a well-known questionnaire that measures the severity of symptoms, physical functioning and patient's satisfaction in lumbar spinal stenosis. This study aimed to translate and validate the SSS in Iran. METHODS: A prospective clinical validation study was performed. Forward-backward procedure was applied to translate the original questionnaires into Persian. A sample of patients with lumbar spinal stenosis completed the questionnaire twice: at pre- and postoperative (6 months follow-up) assessments. To test reliability the internal consistency was assessed by the Cronbach's alpha coefficient. Validity was evaluated using the known groups comparison. In addition the Oswestry Disability Index was used to perform convergent validity. RESULTS: In all 121 patients were entered into the study. The mean age of patients was 62.3 (SD=10.2) years. The Cronbach's alpha coefficient for the SSS was 0.88. Validity was performed by known groups analysis and showed satisfactory results. The instrument discriminated well between the subgroups of patients who differed in age, severity of lumbar spinal stenosis, and the Self-Paced Walking Test (SPWT). The change in the Oswestry Disability Index strongly correlated with the change in patients' scores on the SSS; lending support to its good convergent validity (r=0.82; P<0.001). CONCLUSION: The Iranian version of Swiss Spinal Stenosis Score performed well and the findings suggest that it is a valid measure of symptoms, physical functioning and satisfaction among patients with lumbar spinal stenosis.


Subject(s)
Disability Evaluation , Spinal Stenosis/diagnosis , Adult , Aged , Aged, 80 and over , Female , Humans , Iran , Low Back Pain/etiology , Lumbar Vertebrae/physiopathology , Male , Middle Aged , Pain Measurement/methods , Patient Satisfaction , Prospective Studies , Recovery of Function/physiology , Reproducibility of Results , Spinal Stenosis/complications , Surveys and Questionnaires
2.
Eur Rev Med Pharmacol Sci ; 26(21): 7866-7882, 2022 11.
Article in English | MEDLINE | ID: mdl-36394735

ABSTRACT

OBJECTIVE: Autism Spectrum Disorder (ASD) is a neurodevelopmental disorder that represents a range of aberrant behaviour symptoms such as repetitive behaviours and defects in social communication. The prevalence of ASD has been increasing worldwide and many studies have reported that both genetic and epigenetic factors play an important role in the etiology of this disorder. The aim of this study was to investigate the implementation of DNA methylation and Copy number variation (CNV) in the diagnosis of ASD. PATIENTS AND METHODS: This study was carried out on 14 Saudi autistic children and four of their healthy siblings. Comparative genomic hybridization array was used to identify CNV in chromosome 14 and MethyLight qPCR was used to estimate levels of DNA methylation. RESULTS: The results identified CNVs in six cytobands in chromosome 14 for 13 out of 14 autistic samples: 14q11.1-q11.2, 14q11.2, 14q12, 14q21.1, 14q32.2, and 14q32.33. However, some of these cytobands were also found in normal samples with different sizes. Interestingly, chromosomal abnormalities in 14q11.1-q11.2 was only found in ASD samples. The result also showed an increase in methylation ratio of ASD samples in those CNV regions compared with their siblings. CONCLUSIONS: The findings suggest that CNV in 14q11.1-q11.2 might be a potential target in ASD diagnosis and further work is required to detect which biological pathways are affected.


Subject(s)
Autism Spectrum Disorder , Autistic Disorder , Child , Humans , DNA Copy Number Variations , Comparative Genomic Hybridization/methods , DNA Methylation , Autistic Disorder/diagnosis , Autistic Disorder/genetics , Chromosomes, Human, Pair 14 , Autism Spectrum Disorder/diagnosis , Autism Spectrum Disorder/genetics , Saudi Arabia
3.
Kathmandu Univ Med J (KUMJ) ; 5(4): 511-7, 2007.
Article in English | MEDLINE | ID: mdl-18604085

ABSTRACT

OBJECTIVES: To assess the effect of cigarette smoking on lipid peroxidation induced oxidative stress, antioxidants, uric acid and blood sugar in normal subjects. METHODS: The study included 61 normal subjects with regular smoking habit and 57 never-smokers normal subjects matched in respect to socio-economic status, age and BMI. Information regarding smoking habit and other personal details were collected by oral questionnaire. Total antioxidant activity (TAA), reduced glutathione (GSH), alpha-tocopherol (alpha-T), ascorbic acid (AA), uric acid (UA), plasma and urinary thiobarbituric acid reactive substances (TBARS), fasting blood sugar (FBS) and urinary creatinine (Cr) were estimated by standard procedures in both the groups. Ferric Reducing Antioxidant Power (FRAP) procedure is used to estimate TAA which measures total dietary antioxidants. Statistical analysis was done with SPSS version 10. RESULTS: The mean pack years smoked by smokers was 14.4 +/- 15.8. The plasma TBARS level in smokers and never-smokers was 2.6 +/- 0.8 and 2.5 +/- 0.6 micromol/L respectively. The respective figure for urinary TBARS level was 4.6 +/- 2.7 and 3.7 +/- 1.4 micromol/gmCr. Smokers did not show any significant difference from never-smokers with respect to GSH, alpha-T, AA, plasma TBARS and FBS. However, the smokers had significantly lower levels of TAA (p<0.05) and raised level of urinary TBARS (p<0.05) and uric acid (p<0.01) as compared to never-smokers. CONCLUSION: Our study suggests that smoking induces mild lipid peroxidation but the body is able to compensate for it by removing its adducts. Importantly it also indicates enhanced oxidation of purines which are essential components of both DNA and RNA. Dietary antioxidants are consumed to scavenge free radicals (FR) and other reactive species (RS) in smoke. Female smokers are more prone to oxidative insult than male smokers. In summary RS present in smoke induce mild lipid peroxidation but are not the major contributors of redox imbalance in smoke induced toxicity in the selected subjects.


Subject(s)
Biomarkers/metabolism , Lipid Peroxidation , Smoking/metabolism , Adult , Antioxidants/metabolism , Ascorbic Acid/blood , Blood Glucose/metabolism , Creatinine/urine , Female , Glutathione/blood , Humans , Male , Nepal , Oxidative Stress , Surveys and Questionnaires , Thiobarbituric Acid Reactive Substances/metabolism , Uric Acid/metabolism
4.
Kathmandu Univ Med J (KUMJ) ; 4(3): 302-6, 2006.
Article in English | MEDLINE | ID: mdl-18603923

ABSTRACT

OBJECTIVES: To assess vitamin C status by determining plasma ascorbic acid level in 55 cancer patients and 55 matched normal subjects serving as control. METHODS: The proven cancer patients were selected from those attending Manipal Teaching Hospital, Pokhara. Matched controls were from the staff of Manipal Teaching Hospital or attendants of the patients. Plasma ascorbic acid was determined by the method of Natelson. Unpaired student 't' test was used for the statistical evaluation. Statistical analysis was done by SPSS version 9 software. RESULTS: The mean level of vitamin C in normal subjects and patients was 1.03+/-0.26 mg/dl and 0.90+/-0.30 mg/dl respectively. None of the subjects in either group had deficient status (<0.2 mg/dl). Although its status was normal in both the groups but patients had lower level than normal subjects. Smokers and alcohol consumers had significantly lower level than non-smoker and non-alcoholics. CONCLUSION: In the local population, vitamin C deficiency is not an etiologic factor in malignancy. Smoking and alcohol adversely affects the status of this vitamin.


Subject(s)
Ascorbic Acid Deficiency/complications , Ascorbic Acid Deficiency/epidemiology , Neoplasms/etiology , Age Distribution , Aged , Alcohol Drinking/adverse effects , Antioxidants/metabolism , Ascorbic Acid/blood , Ascorbic Acid Deficiency/blood , Case-Control Studies , Female , Hospitals, Teaching , Humans , Male , Middle Aged , Neoplasms/epidemiology , Nepal/epidemiology , Nutrition Assessment , Nutrition Policy , Nutritional Requirements , Nutritional Status , Population Surveillance , Risk Factors , Sex Distribution , Smoking/adverse effects , Socioeconomic Factors
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