Adiponectin and C-reactive protein are positively associated with microalbuminuria in an adult Caucasian population
Détails
ID Serval
serval:BIB_3B4969CADEA7
Type
Actes de conférence (partie): contribution originale à la littérature scientifique, publiée à l'occasion de conférences scientifiques, dans un ouvrage de compte-rendu (proceedings), ou dans l'édition spéciale d'un journal reconnu (conference proceedings).
Sous-type
Poster: résume de manière illustrée et sur une page unique les résultats d'un projet de recherche. Les résumés de poster doivent être entrés sous "Abstract" et non "Poster".
Collection
Publications
Institution
Titre
Adiponectin and C-reactive protein are positively associated with microalbuminuria in an adult Caucasian population
Titre de la conférence
78. Jahresversammlung der Schweizerischen Gesellschaft für Innere Medizin
Adresse
Basel, Switzerland, 19.-21. Mai 2010
ISBN
1424-3784[print] ; 1424-4020[electronic]
Statut éditorial
Publié
Date de publication
2010
Volume
10
Série
Swiss Medical Forum = Forum Médical Suisse
Pages
29S
Langue
anglais
Résumé
Objective: Microalbuminuria (MAU) is a marker of early kidney injury
and cardiovascular risk. We assessed the association of MAU with
plasma adiponectin, leptin and hsCRP, as inflammatory markers,
accounting for hypertension, diabetes and obesity.
Design and methods: Population based, cross-sectional study in
Caucasian subjects aged 35 to 75 years in Lausanne, Switzerland.
MAU, measured on spot morning urine, was used either as a
continuous (MAU) or dichotomized variable (MA defined as MAU
>2.5 and >3.5 mg/mmol creatinine in men and women, respectively).
Results: The 2955 women (age 53.3 ± 10.7, mean ± SD years) had
mean body mass index (BMI) 24.9 ± 4.5 kg/m. The 2479 men (age 53.1
± 10.8 years) had mean BMI 27.0 ± 3.9 kg/m². Median hsCRP was
1.3 and 1.3 mg/L, median adiponectin 6.2 and 10.6 mg/mL in men and
women, respectively. MA prevalence was 4.9% in women and 9.8%
in men. In multivariate regression analysis adjusting for potential
confounders (age, sex, hypertension, diabetes, eGFR, BMI, percent
fat mass, insulin and smoking), log-transformed MAU was positively
associated with hsCRP (P <0.001) and adiponectin (P = 0.002), but not
with leptin. The association of adiponectin with MAU was stronger in
subjects with low hsCRP, and vice versa (P interaction <0.001).
Conclusion: Adiponectin and hsCRP are significant positive
determinants of MAU, independently of diabetes, hypertension and fat
mass. A negative interaction between hsCRP and adiponectin was
found for their effect on MAU. Whether hyperadiponectinemia represents
an adequate protective response to vascular stress or has negative
causal impact on the development of MAU should be assessed in
further studies.
and cardiovascular risk. We assessed the association of MAU with
plasma adiponectin, leptin and hsCRP, as inflammatory markers,
accounting for hypertension, diabetes and obesity.
Design and methods: Population based, cross-sectional study in
Caucasian subjects aged 35 to 75 years in Lausanne, Switzerland.
MAU, measured on spot morning urine, was used either as a
continuous (MAU) or dichotomized variable (MA defined as MAU
>2.5 and >3.5 mg/mmol creatinine in men and women, respectively).
Results: The 2955 women (age 53.3 ± 10.7, mean ± SD years) had
mean body mass index (BMI) 24.9 ± 4.5 kg/m. The 2479 men (age 53.1
± 10.8 years) had mean BMI 27.0 ± 3.9 kg/m². Median hsCRP was
1.3 and 1.3 mg/L, median adiponectin 6.2 and 10.6 mg/mL in men and
women, respectively. MA prevalence was 4.9% in women and 9.8%
in men. In multivariate regression analysis adjusting for potential
confounders (age, sex, hypertension, diabetes, eGFR, BMI, percent
fat mass, insulin and smoking), log-transformed MAU was positively
associated with hsCRP (P <0.001) and adiponectin (P = 0.002), but not
with leptin. The association of adiponectin with MAU was stronger in
subjects with low hsCRP, and vice versa (P interaction <0.001).
Conclusion: Adiponectin and hsCRP are significant positive
determinants of MAU, independently of diabetes, hypertension and fat
mass. A negative interaction between hsCRP and adiponectin was
found for their effect on MAU. Whether hyperadiponectinemia represents
an adequate protective response to vascular stress or has negative
causal impact on the development of MAU should be assessed in
further studies.
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Création de la notice
21/02/2011 16:49
Dernière modification de la notice
20/08/2019 13:31