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Correspondence
Comment on: Morbidity and mortality associated with the restrictive spirometric pattern: a longitudinal study
  1. Simone Scarlata1,
  2. Claudio Pedone1,
  3. Filippo L Fimognari1,2,
  4. Vincenzo Bellia3,
  5. Francesco Forastiere4,
  6. Raffaele Antonelli Incalzi1,5
  1. 1Unit of Respiratory Pathophysiology, Chair of Geriatrics, University Campus Bio-Medico, Rome, Italy
  2. 2Unit of Respiratory Physiopathology, Internal Medicine Division, Ospedale ‘L Parodi Delfino’, Colleferro, Rome, Italy
  3. 3Institute of General Medicine and Pneumology, Università di Palermo, Palermo, Italy
  4. 4Department of Epidemiology, Roma E Health Authority, Rome, Italy
  5. 5San Raffaele Foundation, Cittadella della Carita, Taranto, Italy
  1. Correspondence to Simone Scarlata, Servizio di Fisiopatologia Respiratoria, Università Campus Bio-Medico, Via A. del Portillo, 200, Rome, Italy; s.scarlata{at}unicampus.it

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We read with interest the paper by Guerra et al1 profiling the demographic/clinical characteristics and prospectively assessing the prognosis of subjects with a restrictive spirometric pattern enrolled in the TESAOD population-based study. The manuscript has the merit of following up a large number of patients for 14 years and investigating how selected co-morbidities are relevant to survival.2

The results of this study deserve comparison with those published in 2008 by our research group on 1265 subjects aged 65–97 years.3 First, in an older population (mean age 73.4 years) we found a comparable prevalence of restriction at spirometry (12% vs 10.9%), although restriction is an age-related phenomenon and, thus, is expected to be much lower in the younger population (ie, 6.6% in a population aged 42.2 years4). Secondly, the study by Guerra and colleagues strongly reproduces the increased mortality risk rates (MRRs) observed in our work: for all (HR 1.89; 95% CI 1.15 to 3.11 (Scarlata et al) vs HR 1.7; 95% CI 1.3 to 2.3 (Guerra et al)), cardiac (MRR 1.51; 95% CI 0.60 to 3.78 (Scarlata et al) vs HR 2.0; 95% CI 1.3 to 3.1 (Guerra et al)) and cerebrovascular (MRR 4.79; 95% CI 1.54 to 14.84 (Scarlata et al) vs HR 2.4; 95% CI 0.9 to 6.3 (Guerra et al)). This finding is consistent with restrictive lung dysfunction affecting survival in a predictable manner.

At variance with our study, that of Guerra and colleagues lacks information about clinical correlates of restrictive pulmonary disease. The Cox proportional hazard models are adjusted only for sex, age and body mass index, but not for concomitant conditions known to be associated with restriction. Indeed, we found that co-morbidities such as kyphosis of the spine (OR 2.40; 95% CI 1.58 to 3.64) and diabetes mellitus (OR 1.66; 95% CI 1.00 to 2.74) as well as the physical (Activities of Daily Living scale, OR 2.17; 95% CI 1.32 to 3.58; 6 minute walking test, OR 1.75; 95% CI 1.15 to 2.67) and cognitive (Mini Mental State Examination, OR 2.05; 95% CI 1.27 to 3.32) status are strong independent correlates of restriction.

In conclusion, the paper by Guerra and colleagues has the merit of confirming that the restrictive spirometric pattern is highly prevalent and is associated with a clinical profile and risk factors differing from those of obstructive lung disease. However, research is needed to expand our knowledge of the mechanisms underlying restriction as well as to explain the link between restriction and frailty. Clarifying these issues will allow the implementation of both guided screening and preventive interventions.

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Footnotes

  • Linked articles 150227.

  • Competing interests None.

  • Provenance and peer review Not commissioned; not externally peer reviewed.

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