High Levels of hsCRP are Associated With Carbohydrate Metabolism Disorder
Author
dc.contributor.author
Leiva, Elba
Author
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Mujica, Verónica
es_CL
Author
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Brito, Katherine
es_CL
Author
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Palomo, Iván
es_CL
Author
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Orrego, Roxana
es_CL
Author
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Moore Carrasco, Rodrigo
es_CL
Author
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Vásquez, Marcela
es_CL
Author
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Guzmán, Luis
es_CL
Author
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Núñez, Sergio
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Author
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Díaz, Nora
es_CL
Author
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Icaza, Gloria
es_CL
Author
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Arredondo Olguín, Miguel Armando
es_CL
Admission date
dc.date.accessioned
2014-01-09T20:57:47Z
Available date
dc.date.available
2014-01-09T20:57:47Z
Publication date
dc.date.issued
2011
Cita de ítem
dc.identifier.citation
Journal of Clinical Laboratory Analysis 25 : 375–381 (2011)
en_US
Identifier
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doi: 10.1002/jcla.20455
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/124058
General note
dc.description
Aim: To determine risk parameters associated
with high values of high sensitive
C-reactive protein (hsCRP) in subjects with
different glucose fasting levels. Methods:
Anthropometric parameters, arterial pressure,
glycemia, lipid profile, uric acid, and
hsCRP were studied in a population of 513
individuals between 40 and 65 years.
Results: In total, 349 (68.0%) were normoglycemic
(NG); 113 (22.0%) had impaired
fasting glucose (IFG); and 51 (9.9%) were
diabetic subjects. A multivariate linear
regression analysis showed that the natural
logarithm of hsCRP was associated
significantly with glycemia levels
(P50.009), uric acid (P50.001), diastolic
blood pressure (P50.011), smoking habit
(P50.021), BMI (Po0.001), and sex
(Po0.001). One-third of the NG subjects
had high hsCRP levels. A multiple logistic
regression analysis showed that sex and
BMI were variables related to high levels of
hsCRP in subjects with IFG and NG. In NG
subjects, uric acid levels were associated
with risk of presenting high hsCRP levels
and were higher in women than men. In NG
women, ROC curves analysis identified a
uric acid level of 3.9 mg/dl as a cut-off point
to predict a high value of hsCRP. Those
individuals with uric acid values higher than
3.9 mg/dl and normal glycemia had 3.5-fold
more risk of having hsCRP levels over
3.0 mg/l. Conclusions: We sustain that high
levels of hsCRP are associated with disturbance
in carbohydrate metabolism. In
addition, we believe that in low cardiovascular
risk population, such as NG women,
uric acid levels above 3.9 mg/dl might
represent a signal of possible pro-inflammatory
state and cardiovascular risk.
en_US
Abstract
dc.description.abstract
Aim: To determine risk parameters associated
with high values of high sensitive
C-reactive protein (hsCRP) in subjects with
different glucose fasting levels. Methods:
Anthropometric parameters, arterial pressure,
glycemia, lipid profile, uric acid, and
hsCRP were studied in a population of 513
individuals between 40 and 65 years.
Results: In total, 349 (68.0%) were normoglycemic
(NG); 113 (22.0%) had impaired
fasting glucose (IFG); and 51 (9.9%) were
diabetic subjects. A multivariate linear
regression analysis showed that the natural
logarithm of hsCRP was associated
significantly with glycemia levels
(P50.009), uric acid (P50.001), diastolic
blood pressure (P50.011), smoking habit
(P50.021), BMI (Po0.001), and sex
(Po0.001). One-third of the NG subjects
had high hsCRP levels. A multiple logistic
regression analysis showed that sex and
BMI were variables related to high levels of
hsCRP in subjects with IFG and NG. In NG
subjects, uric acid levels were associated
with risk of presenting high hsCRP levels
and were higher in women than men. In NG
women, ROC curves analysis identified a
uric acid level of 3.9 mg/dl as a cut-off point
to predict a high value of hsCRP. Those
individuals with uric acid values higher than
3.9 mg/dl and normal glycemia had 3.5-fold
more risk of having hsCRP levels over
3.0 mg/l. Conclusions: We sustain that high
levels of hsCRP are associated with disturbance
in carbohydrate metabolism. In
addition, we believe that in low cardiovascular
risk population, such as NG women,
uric acid levels above 3.9 mg/dl might
represent a signal of possible pro-inflammatory
state and cardiovascular risk.