The Swedish α1-Antitrypsin Screening Study: Health Status and Lung and Liver Function at Age 34
Hanan A Tanash1, Meltem Nystedt-Düzakin1, Laura Cano Montero1
11 Department of Respiratory Medicine and Allergology and.
Insights
Individuals with alpha-1-antitrypsin (AAT) deficiency had lower smoking rates but similar lung function and respiratory symptoms compared to controls at age 34. This long-term follow-up highlights AAT deficiency
Area of Science:
- Pulmonary Medicine
- Genetics
- Epidemiology
Background:
- A long-term Swedish study screened newborns for alpha-1-antitrypsin (AAT) deficiency between 1972-1974.
- A cohort of 127 severe (PiZZ) and 54 moderate (PiSZ) AAT-deficient individuals was followed.
- Regular follow-ups were conducted to monitor health outcomes.
Purpose of the Study:
- To compare smoking habits, quality of life, respiratory symptoms, and lung/liver function at age 34.
- To assess outcomes in AAT-deficient individuals versus 300 age-matched controls (PiMM).
- To investigate the long-term health impact of AAT deficiency.
Main Methods:
- Participants completed questionnaires on smoking and respiratory symptoms.
- Spirometry (FEV1, FVC) and blood tests were performed.
- Health-related quality of life was measured using the St. George's Respiratory Questionnaire (SGRQ).
Main Results:
- No significant differences in lung function (FEV1, FVC) were observed between AAT deficiency groups and controls.
- Smoking frequency was significantly lower in AAT-deficient individuals (PiZZ/PiSZ) compared to controls (PiMM).
- While liver enzyme levels were generally normal, PiZZ subjects showed higher gamma-glutamyl transpeptidase and albumin levels than PiMM.
Conclusions:
- AAT deficiency did not correlate with differences in lung function or respiratory symptoms at age 34.
- Individuals with AAT deficiency exhibited a notably lower prevalence of smoking.
- The findings suggest that reduced smoking may mitigate some long-term health risks associated with AAT deficiency.
Rationale:
All Swedish newborn infants were screened for α1-antitrypsin (AAT) deficiency between 1972 and 1974. The cohort of 127 individuals with severe AAT deficiency (PiZZ) and 54 with moderate AAT deficiency (PiSZ) has been followed up regularly.
Objectives:
To compare smoking habits, quality of life, respiratory symptoms, and lung and liver function at the age of 34 years in this cohort and among 300 age-matched control subjects randomly selected from the Swedish population registry.
Methods:
The study participants answered a questionnaire on smoking habits and symptoms; underwent spirometry, including FEV1 and FVC; and provided blood samples. Health-related quality of life was assessed by using the St. George's Respiratory Questionnaire (SGRQ).
Measurements And Main Results:
One hundred sixteen PiZZ, 48 PiSZ, and 229 control subjects (normal AAT level [PiMM]) answered the questionnaire. Eighty-eight PiZZ (76%), 36 PiSZ (75%), and 144 PiMM (63%) subjects had never smoked (P = 0.02). No significant differences were found in lung function parameters between the protease inhibitor (Pi) subgroups, nor were any discovered between the smoking subgroups. In all Pi subgroups, the symptom score on the SGRQ was significantly lower in ever-smokers than in never-smokers (P = 0.01 for PiZZ, P = 0.009 for PiSZ, and P = 0.01 for PiMM). The mean plasma levels of liver enzymes and albumin were within normal range in all Pi subgroups. However, the mean γ-glutamyl transpeptidase and albumin levels were significantly higher in the PiZZ than in the PiMM subjects (P < 0.05).
Conclusions:
In this population-based study, no differences in lung function or symptoms were found between subjects with AAT deficiency and control subjects, but smoking frequency was significantly lower among the subjects with AAT deficiency than in the controls at age 34 years.
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