Clinical Features Most Likely To Be Associated With The Laboratory Diagnosis Of Alpha-1-Antitrypsin Deficiency

Author(s):  
Adriano Tonelli ◽  
Farshid Rouhani ◽  
Cathy Charleston ◽  
Natasha Viranovskaya ◽  
Regina Wolper ◽  
...  
BMJ Open ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. e036045
Author(s):  
Diana Crossley ◽  
James Stockley ◽  
Charlotte E Bolton ◽  
Nicholas S Hopkinson ◽  
Ravi Mahadeva ◽  
...  

ObjectivesTo establish a database network for the study of alpha-1 antitrypsin deficiency (AATD) and compare the results to CT lung density as the most direct measure of emphysema.DesignA central electronic database was established to permit the upload of anonymised patient data from remote sites. Prospectively collected CT data were recorded onto disc, anonymised, analysed at the coordinating centre and compared with the clinical features of the disease.SettingTertiary referral centres with expertise in the management of AATD focused on academic Biomedical Research Units and Wellcome Clinical Research Facilities.ParticipantsData were collected from 187 patients over 1 year from eight UK academic sites. This included patient demographics, postbronchodilator physiology, health status and CT. Analysis was undertaken at the coordinating centre in Birmingham.ResultsPatient recruitment in the 12 months reached 94% of target (set at 200) covering the whole spectrum of the disease from those with normal lung function to very severe chronic obstructive lung disease. CT scan suitable for analysis was available from 147 (79%) of the patients. CT density, analysed as the threshold for the lowest 15% of lung voxels, showed statistically significant relationships with the objective physiological parameters of lung function as determined by spirometric Global Initiative for Chronic Obstructive Lung Disease (GOLD) severity staging (p<0.001) and carbon monoxide gas transfer (p<0.01). Density also correlated with subjective measures of quality of life (p=0.02).ConclusionsEstablishment of the network for data collection and its transfer was highly successful facilitating future collaboration for the study of this rare disease and its management. CT densitometry correlated well with the objective clinical features of the disease supporting its role as the specific marker of the associated emphysema and its severity. Correlations with subjective measures of health, however, were generally weak indicating other factors play a role.


Author(s):  
Dino Hadzic

The chapter on alpha-1 antitrypsin deficiency describes the genetics and the pathogenesis of this disorder as well as the clinical features of the homozygous PiZ alpha-1 antitrypsin deficiency and its management.


2013 ◽  
Vol 2013 ◽  
pp. 1-7 ◽  
Author(s):  
Federica Zarrilli ◽  
Ausilia Elce ◽  
Manuela Scorza ◽  
Sonia Giordano ◽  
Felice Amato ◽  
...  

Liver inherited diseases are a group of genetically determined clinical entities that appear with an early chronic liver involvement. They include Wilson’s disease (hepatolenticular degeneration), hereditary hemochromatosis, and alpha-1-antitrypsin deficiency. In addition, cystic fibrosis, although it is not specifically a liver disease, may cause a severe liver involvement in a significant percentage of cases. For all these pathologies, the disease gene is known, and molecular analysis may contribute to the unequivocal diagnosis. This approach could avoid the patient invasive procedures and limit complications associated with a delay in diagnosis. We review liver inherited diseases on the basis of the genetic defect, focusing on the contribution of molecular analysis in the multistep diagnostic workup.


Thorax ◽  
2014 ◽  
Vol 69 (Suppl 2) ◽  
pp. A100-A100 ◽  
Author(s):  
S. Vayalapra ◽  
R. Edgar ◽  
D. Griffiths ◽  
R. Stockley ◽  
A. Turner

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