Hyperlipidaemia prevalence and cholesterol control in obstructive sleep apnoea: Data from the European sleep apnea database (ESADA).


Journal

Journal of internal medicine
ISSN: 1365-2796
Titre abrégé: J Intern Med
Pays: England
ID NLM: 8904841

Informations de publication

Date de publication:
12 2019
Historique:
pubmed: 2 7 2019
medline: 26 5 2020
entrez: 2 7 2019
Statut: ppublish

Résumé

Obstructive sleep apnoea (OSA) and hyperlipidaemia are independent risk factors for cardiovascular disease. This study investigates the association between OSA and prevalence of hyperlipidaemia in patients of the European Sleep Apnea Database (ESADA) cohort. The cross-sectional analysis included 11 892 patients (age 51.9 ± 12.5 years, 70% male, body mass index (BMI) 31.3 ± 6.6 kg/m Hyperlipidaemia prevalence increased from 15.1% in subjects without OSA to 26.1% in those with severe OSA, P < 0.001. Corresponding numbers in patients with diabetes were 8.5% and 41.5%, P < 0.001. Compared with ODI quartile I, patients in ODI quartiles II-IV had an adjusted OR (95% CI) of 1.33 (1.15-1.55), 1.37 (1.17-1.61) and 1.33 (1.12-1.58) (P < 0.001), respectively, for hyperlipidaemia. Obesity was defined as a significant risk factor for hyperlipidaemia. Subgroups of OSA patients with cardio-metabolic comorbidities demonstrated higher prevalence of HL. In addition, differences in hyperlipidaemia prevalence were reported in European geographical regions with the highest prevalence in Central Europe. Obstructive sleep apnoea, in particular intermittent hypoxia, was independently associated with the prevalence of hyperlipidaemia diagnosis.

Sections du résumé

BACKGROUND AND OBJECTIVE
Obstructive sleep apnoea (OSA) and hyperlipidaemia are independent risk factors for cardiovascular disease. This study investigates the association between OSA and prevalence of hyperlipidaemia in patients of the European Sleep Apnea Database (ESADA) cohort.
METHODS
The cross-sectional analysis included 11 892 patients (age 51.9 ± 12.5 years, 70% male, body mass index (BMI) 31.3 ± 6.6 kg/m
RESULTS
Hyperlipidaemia prevalence increased from 15.1% in subjects without OSA to 26.1% in those with severe OSA, P < 0.001. Corresponding numbers in patients with diabetes were 8.5% and 41.5%, P < 0.001. Compared with ODI quartile I, patients in ODI quartiles II-IV had an adjusted OR (95% CI) of 1.33 (1.15-1.55), 1.37 (1.17-1.61) and 1.33 (1.12-1.58) (P < 0.001), respectively, for hyperlipidaemia. Obesity was defined as a significant risk factor for hyperlipidaemia. Subgroups of OSA patients with cardio-metabolic comorbidities demonstrated higher prevalence of HL. In addition, differences in hyperlipidaemia prevalence were reported in European geographical regions with the highest prevalence in Central Europe.
CONCLUSION
Obstructive sleep apnoea, in particular intermittent hypoxia, was independently associated with the prevalence of hyperlipidaemia diagnosis.

Identifiants

pubmed: 31260567
doi: 10.1111/joim.12952
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

676-688

Investigateurs

P Steiropoulos (P)
J Verbraecken (J)
E Petiet (E)
G Trakada (G)
J M Montserrat (JM)
I Fietze (I)
T Penzel (T)
D Rodenstein (D)
J F Masa (JF)
S Schiza (S)
B Kent (B)
W T McNicholas (WT)
S Ryan (S)
R L Riha (RL)
J A Kvamme (JA)
R Schulz (R)
D Zou (D)
J L Pépin (JL)
P Levy (P)
S Bailly (S)
L Lavie (L)
P Lavie (P)
M S Tasbakan (MS)
G Varoneckas (G)
P Joppa (P)
R Tkacova (R)
F Barbé (F)
C Lombardi (C)
G Parati (G)
M Drummond (M)
M van Zeller (M)
O Marrone (O)
M Petitjean (M)
M Pretl (M)
A Vitols (A)
Z Dogas (Z)
T Galic (T)
U Anttalainen (U)
T Saaresranta (T)
R Plywaczewski (R)
P Bielicki (P)

Informations de copyright

© 2019 The Association for the Publication of the Journal of Internal Medicine.

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Auteurs

C Gunduz (C)

From the, Department of Chest Diseases, Biruni University, Istanbul, Turkey.
Department of Chest Diseases, Ege University, Izmir, Turkey.

O K Basoglu (OK)

Department of Chest Diseases, Ege University, Izmir, Turkey.

J Hedner (J)

Center for Sleep and Vigilance Disorders, Sahlgrenska Academy, Gothenburg University, Gothenburg, Sweden.
Sleep Disorders Center, Pulmonary Department, Sahlgrenska University Hospital, Gothenburg, Sweden.

M R Bonsignore (MR)

Biomedical Department of Internal and Specialist Medicine (DiBiMIS), Section of Pneumology, University of Palermo, Palermo, Italy.
CNR Institute of Biomedicine and Molecular Immunology, Palermo, Italy.

H Hein (H)

Sleep Disorders Center, St. Adolf Stift, Reinbeck, Germany.

R Staats (R)

Department of Respiratory Medicine, Hospital de Santa Maria, Lisbon, Portugal.

I Bouloukaki (I)

Sleep Disorders Unit, Department of Respiratory Medicine, University of Crete, Heraklion, Greece.

G Roisman (G)

Sleep Disorders Center, Antoine-Beclere Hospital, Clamart, France.

A Pataka (A)

Respiratory Failure Unit, G. Papanikolaou Hospital, Thessaloniki, Greece.

P Sliwinski (P)

2nd Department of Respiratory Medicine, Institute of Tuberculosis and Lung Diseases, Warsaw, Poland.

O Ludka (O)

Department of Cardiology, University Hospital Brno, Brno, Czech Republic.
International Clinical Research Center, St. Ann's University Hospital, Brno, Czech Republic.

J L Pepin (JL)

INSERM U1042, CHU de Grenoble, Université Grenoble Alpes, Grenoble, France.

L Grote (L)

Center for Sleep and Vigilance Disorders, Sahlgrenska Academy, Gothenburg University, Gothenburg, Sweden.
Sleep Disorders Center, Pulmonary Department, Sahlgrenska University Hospital, Gothenburg, Sweden.

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