Article ID Journal Published Year Pages File Type
3400036 Egyptian Journal of Chest Diseases and Tuberculosis 2015 11 Pages PDF
Abstract

AimTo compare the lung function parameters of poorly controlled type-1-diabetes-mellitus (T1DM) patients with age-; height and sex-matched healthy-non-smokers (HNS).Population and methodsSubjects aged 35–60 Yrs who have a poorly controlled T1DM (glycated-Haemoglobin level >7%) with a disease history of more than 10 Yrs (n = 14) and HNS subjects (n = 14) were recruited. Clinical, anthropometric and fasting biological data were collected. Plethysmographic data (flows, volumes, estimated-lung-age (ELA), lung-capacity-to-transfer-carbon-monoxide (DLCO)) were measured. Large-airway-obstructive-ventilatory-defect (LAOVD) was defined as first–second-forced-expiratory-volume (FEV1)/forced-vital-capacity (FVC) below the lower-limit-of-normal (LLN). Restrictive-ventilatory-defect (RVD) was defined as total-lung-capacity (TLC) < LLN. Lung-hyperinflation was defined as residual-volume (RV) > upper-limit-of-normal. Student t-test and chi-2 test were used to compare plethysmographic data and profiles of the two groups.ResultsThe two groups were matched in chronological-lung-age (CLA) (respectively 47 ± 7 vs. 50 ± 8 Yrs) and sex (7 males and 7 females in each group) and height. Compared to the HNS group, the T1DM one had significantly lower FEV1, FVC, slow-vital-capacity and maximal-mid-expiratory-flow (respectively 99 ± 11% vs. 83 ± 11%, 99 ± 9% vs. 86 ± 11%, 80 ± 8% vs. 67 ± 15% and 98 ± 23% vs. 72 ± 23%), had significantly higher TLC and RV (respectively, 105 ± 20% vs. 123 ± 24% and 108 ± 22% vs. 131 ± 24%) and had significantly higher percentage of subjects with lung-hyperinflation (7.1% vs. 43.0%). Both groups had similar percentages of LAOVD and RVD and similar corrected DLCO values. ELA of the T1DM group (57 ± 10 Yrs) was significantly higher than CLA.ConclusionPoorly controlled T1DM seems to alter ventilatory mechanics without effect on the alveolo-capillary-membrane. In addition, it accelerates the respiratory ageing.

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