]. Respiratory medicine is facing formidable challenges in the 21st century. Indeed, most respiratory medical research is becoming interconnected, translational and transnational, all embedded within so-called "planetary health" [1]. However, renewing estimates and trends from classical, descriptive epidemiology, including how many patients of a given condition are around, and how many are expected in the future, remain ongoing chores. Continuous updates from the World Health Organization's Global Burden of Disease initiative reiterate that respiratory diseases rank high in morbidity and mortality, even with widespread underdiagnosis [2]. Perhaps there is no better example of a respiratory condition that requires further epidemiological and population refreshing than severe α 1-antitrypsin deficiency (AATD). Severe AATD is considered a rare disease, which is defined as any disease that affects less than 1 in 2000 individuals [3]. The prevalence of AATD in the general population in Europe is approximately 1 in 2000-5000. Despite the recognised potential for life-threatening disease at a young age, this condition continues to be largely underdiagnosed; on a worldwide scale it is estimated that only 0.35% of expected AATD cases are detected [3]. Moreover, the majority of individuals continue to experience a substantial delay of several years before diagnosis [4]. The number of cases of AATD and chronic obstructive pulmonary disease (COPD) worldwide has been the subject of intense debate in respiratory medicine. Based on an analysis of published genetic epidemiological surveys, DE SERRES et al. [5] concluded back in 2002 that "… it has been estimated that 3.4 million individuals in the world have an AATD genotype that leads to a deficiency of this protein". From a distance, this estimate appears to be quite accurate, nowadays as high as 3.3 million, by applying the estimate that AATD accounts for 1% of all 332 million COPD cases worldwide from the Global Burden of Disease study [2]. More recently, genetic epidemiological studies on the prevalence of AATD in 97 countries [6] identified Latvia as having the highest prevalence of deficiency alleles: PI*S 31.3 per 1000 population and PI*Z 45.1 per 1000 population. Although considerable variation was apparent between geographic regions and between countries in the same continent, the overall result was the same: AATD can be identified in any region and in any country, if it is searched for actively. However, data on the current prevalence and estimated numbers of AATD patients are missing in many countries, and we need to identify these patients and make sure that they do not smoke, or help them with smoking cessation first, before considering other management decisions.