Re-Establishing Stage 0 of COPD-Juniper publishers
JUNIPER PUBLISHERS-OPEN ACCESS INTERNATIONAL JOURNAL OF PULMONARY & RESPIRATORY SCIENCES
Opinion
Chronic Obstructive Pulmonary Disease (COPD) is a
prevalent, with greater morbidity and mortality disease [1]. COPD is the
fourth leading cause of death, with more than 3 million deaths per year
globally [2]. Its economic burden is enormous and had been the greatest
challenge for all Health Systems in the world [3].
According to the last GOLD document, COPD is defined
as: “a common, preventable and treatable disease that is characterized
by persistent respiratory symptoms and airflow limitation that is due to
airway and/or alveolar abnormalities usually caused by significant
exposure to noxious particles and gases” [1,4].
The progressive airflow limitation has been shown by
the classical work of Fletcher and Peto in the seventies and became the
basis of the introduction of spirometry into the diagnosis of COPD
[5,6]. A ratio of FEV1/FVC below 0.7 is now required to classify a
patient with symptoms such as dyspnea, cough and sputum as COPD [1,4].
Although the “preventable” element is stated in the
definition, the disease is usually diagnosed very late and this has
significant consequences on the natural history of the disease [4]. It
is well known that the susceptible individual in order to develop the
disease needs to be exposed to risk factors for long time, more than a
decade [1,4,6-7].
During this prolong pre-clinical period of the
natural history of the disease significant changes occurs in the lungs
on molecular and cellular level [8-12]. The small airways, in the
periphery of the lungs, are usually the site where the initiation of
those alterations could be detected [13]. Thereafter, those pathological
changes may proceed towards the larger airways developing the phenotype
of chronic bronchitis or towards the alveoli, causing emphysema or more
commonly in both directions, developing the frequent phenotype of both
entities (chronic bronchitis and emphysema) in the same patient, the so
called COPD patient [14,15].
During this phase of the disease the above
morphological changes produce symptoms such as breathlessness, coughand
sputum. Usually, these symptoms appear well before the functional
changes could be detected by spirometry (FEV1/FVC <0.7). Recent
studies had confirmed these observations showing that current or
ex-smokers with preserved pulmonary function have symptoms,
exacerbations and activity limitation equivalent that seen in COPD
patients [14].
Thus, this early pre-clinical phase, according to the
definition of COPD, is extremely important because if the disease is
detected during this stage and managed appropriately, the natural
history of the disease may be altered immensely. Previously, this
sub-clinical stage was defined as STAGE 0 by the first guideline
documents by GOLD but it disappeared from the subsequent ones [1,15].
Since, during this long pre-clinical phase of the
natural history of the disease the most significant molecular, cellular
and histological changes occur, it would be of great scientific value to
focus our research on it [16].
Therefor, I do recommend the re -establishment of
Stage O of COPD, defining the patients with exposure to risk factors,
having the symptoms of the disease (dyspnea, cough and sputum), but with
preserved lung function. I do believe, that if we have STAGE 0 back in
the guidelines, we will enhance the research on the pathophysiology of
its early phase, in other wards, at the beginning of COPD [16,17]. In
addition, STAGE 0 will increase the awareness of the disease and if the
appropriate measures will be taken ,this would modify the natural
history of COPD, reducing immensely the burden the disease.
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