| 
             | 
         
        
            
                
	
		| 
                     | 
	 
		
                        
			
				
                                     
                                       Interferon- Gamma- Inducible Guanosine Triphosphate Cyclohydrolase 1 (GTP-CH1) Pathway Is Associated with Frailty in Egyptian Elderly  
                                     
                                 | 
			 
			
				| 
                                     
                                 | 
				
                                     
                                 | 
			 
			
				| 
                                    
                                 | 
				
                                    
                                 | 
			 
			
				| 
                                    نویسنده
                                 | 
				
                                    mohamad magda ,ebeid somaia ,khater mohamed shawky ,alsadany mohamad
                                 | 
			 
			
				| 
                                    منبع
                                 | 
				
                                    reports of biochemistry and molecular biology - 2018                                     - دوره : 7          - شماره : 1                    - صفحه:52        -58        
                                 | 
			 
			
			 
			
				| 
                                    چکیده
                                 | 
				
                                      
                                    Background: chronic low-grade inflammation may be a cardinal pathophysiologic feature in the pathogenesis of frailty. interferon-gamma (inf-γ) is an understudied proinflammatory cytokine in frailty that induces many inflammatory pathways including the guanosine triphosphate cyclohydrolase 1 (gtp-ch1) pathway. our aim was to evaluate the gtp-ch1 pathway in egyptian frail elderly subjects. methods: inf-γ, neopterin, and nitric oxide (no) levels were measured in 80 participants. results: both pre-frail and frail subjects had significantly higher levels of inf-γ, neopterin and lower levels of no than the control group. these biomarkers were associated with the risk of frailty with significant odds ratio. conclusions: elevated inf-γ levels in frail subjects may activate the gtp-ch1 pathway. elevated neopterin and reduced no levels correlated with an active gtp-ch1 pathway. the risk of frailty increased with elevated inf-γ and neopterin and decreased with elevated no levels.
                                 | 
			 
			
				| 
                                    کلیدواژه
                                 | 
				
                                    Frailty ,GTP-CH1 pathway ,INF-γ
                                 | 
			 
			
				| 
                                    آدرس
                                 | 
				
                                     ain shams university, faculty of medicine, medical biochemistry department, Egypt, ain shams university, faculty of medicine, geriatrics and gerontology department, Egypt, ain shams university, faculty of medicine, geriatrics and gerontology department, Egypt, ain shams university, faculty of medicine, geriatrics and gerontology department, Egypt 
                                 | 
			 
			
				| 
                                    
                                 | 
				
                                    
                                 | 
			 
			
				| 
                                 | 
				
                                     
                                 | 
			 
			
				| 
                                    
                                 | 
				
                                 | 
			 
		 
		
                     | 
	 
		| 
                     | 
	 
 
             | 
         
                
            
                
	
		| 
                     | 
	 
		
                        
			
				
                                     
                                         
                                     
                                 | 
			 
			
				| 
                                     
                                 | 
				
                                     
                                 | 
			 
			
				| 
                                    Authors
                                 | 
				
                                    
                                 | 
			 
			
				| 
                                    
                                 | 
				
                                      
                                    
                                 | 
			 
			
				| 
                                    
                                 | 
				
                                    
                                 | 
			 
			
				| 
                                 | 
				
                                     
                                 | 
			 
			
				| 
                                    
                                 | 
				
                                 | 
			 
		 
		
                     | 
	 
		| 
                     | 
	 
 
             | 
         
        
            | 
             | 
         
        
            | 
                 
             | 
         
     
                 |