Mankowska A.1,
Sypniewska G.1, Rajewski P.2, Gruszka
M.1
- Department of Laboratory Medicine, Collegium Medicum, Nicolaus
Copernicus University, Bydgoszcz, Poland
- Department of Internal Diseases, E. Warminski City
Hospital, Bydgoszcz, Poland
Correspondence
Aneta Mankowska;
Department of Laboratory Medicine,
Collegium Medicum,
Nicolaus Copernicus University,
Sklodowskiej-Curie 9,
85-094 Bydgoszcz,
Poland;
Phone +48 52 585 40 46;
Fax +48 52 585 36 03;
e-mail: anetha7@poczta.onet.pl

Abstract
Adiponectin reduces oxidative stress, the release of
C-reactive protein and influences on the process of atherogenesis
reducing lipid accumulation in the blood vessels. The findings on
the association of adiponectin with cardiovascular risk are
contradictory. This study aimed to assess the relationship between
adiponectin and indices of cardiovascular risk in women with
excessive body mass.
Adiponectin, hsCRP and lipids were measured in blood samples
obtained from normoglycemic women with excessive body mass
(n=52;BMI≥25 kg/m2) aged 25-40 yrs and age-matched healthy controls
(n=36; BMI<25kg/m2). All subjects underwent blood pressure
examination and anthropometric measurements.
Median concentration of adiponectin in the serum in women with
excessive body mass was significantly lower than in women with
normal weight (10,8 vs 15,5 µg/ml; p<0,01). Similarly, median
serum concentration of triglycerides, hsCRP and blood pressure
values were significantly higher and HDL-cholesterol significantly
lower in women with BMI≥25 kg/m2 in comparison to these with normal
BMI, however only HDL-C and hsCRP were found to be beyond widely
accepted cut-offs. Hypoadiponectinemia in women with
excessive body mass (adiponectin concentration below the 5th
percentile in the control group) was associated predominantly with
abnormally increased median values of hsCRP and blood
pressure. Concentrations of total cholesterol, non-HDL-C
and LDL-C were also significantly higher in women with
excessive body mass and hypoadiponectinemia, however still within
the reference range.
Our results suggest that adiponectin may be used as a prognostic
marker of cardiovascular risk in women with excessive body
mass.
Introduction
Adipose tissue plays a central role in the management of
systemic energy stores as well as in many other processes [1]. This
is in part due to its capacity to store triglycerides but is also a
function of its ability to secrete many bioactive adipocytokines
that have a major impact on energy homeostasis and several other
processes [1, 2]. Adiponectin, secreted exclusively by adipose
tissue, is one of the most important metabolically active cytokine
in relation to its function in cardiovascular system [2,3,4].
Adiponectin has attracted much attention because of its
anti-diabetic, anti-atherogenic and anti-inflammatory effect
[3,5,6]. Low-circulating levels of this adipokine are associated
with multiple metabolic disorders including obesity, insulin
resistance, type 2 diabetes, and cardiovascular disease [7,8,9,10].
Furthermore adiponectin reduces oxidative stress and the release of
C-reactive protein [11,12]. It also influences on the process of
atherogenesis reducing lipid accumulation in the blood vessels
[13]. Recently, a few population-based studies presented results of
adiponectin as a cardiovascular risk factor and its association
with atherosclerosis, stable coronary artery disease and acute
coronary syndromes [2,7,10,14]. Little is known about the
association of adiponectin and such cardiovascular risk
factors such as blood pressure. We aimed to investigate the
relationship between serum adiponectin and indices of
cardiovascular risk in young women with excessive body mass.
Subjects
The study group included 52 young women aged 20-40 yrs with
abnormal body mass, recruited from patients of Department of
Internal Diseases, E. Warminski City Hospital in Bydgoszcz. Study
group consisted of 58 overweight and obese women (BMI≥ 25
kg/m2). The control group (BMI<25 kg/m2) consisted of 38
age-matched women (20-40 yrs) recruited on voluntary basis. Both
groups were characterized by normoglycemia (< 100 mg/dL). We
have accepted the following cut-off values for lipids and hsCRP :
TC<200 mg/dL, HDL-C >50mg/dL, LDL-C<130mg/dL, TG<150
mg/dL, non-HDL-C <160 mg/dL, hsCRP <3mg/L. In each subject
body weight and height were measured and BMI was calculated
(kg/m2); also blood pressure was examined. Women included into the
study had not taken any contraceptives,
anti-inflammatory or other medicines known to affect lipid or
carbohydrate metabolism. The written informed consent from
each participant was obtained and the study was approved by
the Bioethics Committee at Collegium Medicum, Nicolaus Copernicus
University.
Methods
Fasting blood was drawn in the early morning (7.00-9.00 am).
Serum was obtained within less than 1 hour to avoid proteolysis and
stored deep-frozen (-80°C) in small aliquots until assayed but not
longer than 8 months.
Serum was assayed for HDL-cholesterol (HDL-C), triglycerides (TG),
total cholesterol (TC), and glucose (ARCHITECT ci8200, Abbott
Diagnostics). LDL-cholesterol (LDL-C) and non-HDL-C values were
calculated. Serum CRP (hsCRP) concentration was measured by a
high-sensitivity method (BN II, Dade Behring) and adiponectin was
assayed by ELISA (DRG MedTek, R@D).
The height (cm), weight (kg) were measured using standard methods.
Systolic and diastolic blood pressure (BP) were measured according
to standard procedures by trained personnel. The
cut-off value of systolic BP was <130 mmHg and <85mmHg
for diastolic BP.
Statistical methods
All data were presented as mean ± standard deviation (Gaussian
distribution of results) or median and the 25th and 75th percentile
(non-Gaussian distribution). The student t-test and U-Mann-Whitney
test were used to compare differences. Comparison of mean values
between groups were done by ANOVA or Kruskal-Wallis test. P<0,05
was considered statistically significant. Statistical analysis was
performed using Statistica 8.0 for Windows (Stat Soft).
Results
Characteristics of study and control groups is presented
in Table 1. Among measured biochemical parameters only median HDL-C
and CRP concentrations were found to be below or over the accepted
cut-offs. Median serum adiponectin in all women with
excessive body mass (mean BMI 32,6 ±6,1 kg/m2) was
significantly lower than in normal weight women, however this
was especially observed in a subgroup of obese women (BMI 36,9±5,3;
adiponectin 10,1 vs 15,5µg/mL; p<0.02). In overweight
women (BMI 27,5±1,4) and controls adiponectin concentrations were
similar.
Table.1 Characteristics of the study and control
group.

On the basis of the distribution of adiponectin concentration in
the control group of clinically healthy normal weight women we have
accepted the 5th percentile as the cut-off for the lowest
adiponectin. Thus as hypoadiponectinemia the concentration of
adiponectin ≤ 6,02 μg/mL was regarded (Table 2). Among women with
excessive body mass those with hypoadiponectinemia had
abnormally increased median CRP and blood pressure values. Median
concentrations of measured lipid variables such as TC, LDL-C and
non-HDL-C were also significantly higher in hypoadiponectinemia,
however still within the accepted reference range. This was
not the case if similar comparison was performed in a study group
in relation to serum CRP. The 95th percentile cut-off for hsCRP in
the control group was found to be 1,4 mg/L . We have not found any
significant differences between the values of measured
variables in women with BMI≥25 kg/m2 if their CRP concentrations
were over or below the 95th percentile cut-off (results not
shown).
Table.2 Concentration of analyzed variables in relation to
adiponectin

Discussion
In the present study we have investigated whether adiponectin is
related to cardiovascular risk in women with excessive body weight
by analyzing the association of its serum level with
biochemical and clinical variables. Hypoadiponectinemia in
women with excessive BMI was found to be associated with
significantly increased values of blood pressure and hsCRP
concentration, that exceeded the accepted
cut-offs.
Recent data suggest that adiponectin has many defensive
properties against obesity-related hypertension [15,16,17] . Chow
et al demonstrated for the first time an inverse relation
between adiponectin concentration and the future development of
hypertension [18]. They suggested that low adiponectin levels may
play an important role in the pathogenesis of human hypertension.
Low adiponectin levels are associated with increased plasma
concentration of free-fatty acids and hepatic fat content and have
been linked to the development of insulin resistance, which might,
in turn, represent a base for the development of hypertension [19].
Hypoadiponectinemia might influence blood pressure also through
other mechanisms, including endothelial dysfunction and the
activation of the inflammatory cascade [18,19].
Some studies suggested that adiponectin level measurements could
be useful in identifying obese patients at high risk of
dyslipidemia and cardiovascular disease [20]. Our results
also confirm a close association of hypoadiponectinemia
with increased cardiovascular risk related to hs-CRP level.
Moreover, we may suggest that measuring adiponectin seems to offer
additional value over hsCRP, used routinely as the inflammatory
marker, in assessing cardiovascular risk in women with
excessive body mass.
We are aware of the limitation of this study that includes a
relatively small groups; however, our results suggest that
adiponectin may be used as a prognostic marker of cardiovascular
risk in women with excessive body mass.
Acknowledgments
We would like to thank the staff at the Department of Laboratory
Medicine, NC University Hospital for help to perform the
determinations of laboratory parameters. This study was supported
by a grant number 14/2008 from the Collegium Medicum, Nicolaus
Copernicus University in Bydgoszcz, Poland.
References
- Zahorska-Markiewicz B.: Metabolic effects associated with
adipose tissue distribution. Advances in Medical Sciences 2006; 51:
111-114.
- Tuchacz S., Gruchała M., Karbowska J., Kochan Z., Sobiczewski
W., Rynkiewicz A.: Adiponektyna w chorobie wiencowej-przegląd
pismiennictwa. Pol Przegl Kardiol 2007; 9(3): 215-219.
- Strączkowski M.: Adipocytokiny u osob z choroba
wiencowa-przydatny marker diagnostyczny? Kardiologia Pol 2008;
66(11): 1181-1182.
- Lago F., Dieguez C., Gomez-Reino J. et al.: Adipokines as
emerging mediators of immune response and inflammation. Nature Clin
Pract Rheumatol 2007; 3(12): 716-724.
- Kadowaki T., Yamauchi T., Kubota N. et al.: Adiponectin and
adiponectin receptors in insulin resistance, diabetes and the
metabolic syndrome. J Clin Invest 2006; 116(7): 1784-92.
- Whitehead JP., Richards AA., Hickman IJ. et al: Adiponectin--a
key adipokine in the metabolic syndrome.Diabetes Obes Metab. 2006;
8(3):264-80.
- Matsubara M., Maruoka S., Katayose S.: Inverse relationship
between plasma adiponectin and leptin concentrations in
normal-weight and obese women. Eur J Endocrinol 2002; 147(2):
173-80.
- Silha JV., Krsek M., Skrha JV. et al.: Plasma resistin,
adiponectin and leptin levels in lean and obese subjects:
correlations with insulin resistance. Eur J Endocrinol 2003;
149(4): 331-5.
- Ouchi N, Kihara S, Funahashi T, Matsuzawa Y, Walsh K.: Obesity,
adiponectin and vascular inflammatory disease. Curr Opin Lipidol.
2003; 14(6): 561-6.
- Hopkins TA., Ouchi N., Shibata R., Walsh K.: Adiponectin
Actions in the Cardiovascular System. Cardiovasc Res. 2007; 74(1):
11-18.
- Karastergiou K., Mohamed-Ali V., Jahangiri M., Kaski JC.:
Adiponectin for Prediction of Cardiovascular Risk? Br J Diabetes
Vasc Dis 2009; 9(4): 150-154.
- Devaraj S., Torok N., Dasu MR., Samols D., Jialal I.:
Adiponectin decreases C-reactive protein synthesis and secretion
from endothelial cells: evidence for an adipose tissue-vascular
loop. Arterioscler Thromb Vasc Biol 2008; 28: 1368-74.
- Ouchi N., Kihara S., Funahashi T. et al.: Reciprocal
association of C-reactive protein with adiponectin in blood stream
and adipose tissue. Circulation 2003; 107: 671-674.
- Nakamura Y., Shimada K., Fukuda D., Shimada Y., Ehara S.,
Hirose M., et al. Implications of plasma concentrations of
adiponectin in patients with coronary artery disease. Heart 2004;
90: 528-33.
- Iwashima Y., Katsuya T., Ishikawa K., Ouchi N., Ohishi M.,
Sugimoto K., Fu Y, Motone M., Yamamoto K., Matsuo A., Ohashi K,
Kihara S., Funahashi T.: Hypoadiponectinemia is an independent risk
factor for hypertension. Hypertension 2004; 43: 1318-1323.
- Francischetti EA., Celoria BM., Duarte SF.:.
Hypoadiponectinemia is associated with blood pressure increase in
obese insulinresistant individuals. Metabolism 2007; 56:
1464-1469.
- Chow W-S., Cheung BMY., Tso AWK., Xu A., Wat NMS., Fong CHY.,
Ong LHY, Tam S, Tan KCB., Janus ED., Lam TH., Lam KSL.:
Hypoadiponectinemia as a predictor for the development of
hypertension: a 5-year prospective study. Hypertension2007; 49 :
1455-1461.
- Han SH., Quon MJ., Kim J., Koh KK.: Adiponectin and
cardiovascular disease: response to therapeutic intervention. J Am
Coll Cardiol 2007; 49: 531-538.
- Devaraj S., Swarbrick MM., Singh U., Adams-Huet B., Havel PJ.,
Jialal I.: CRP and adiponectin and its oligomers in the metabolic
syndrome: evaluation of new laboratory-based biomarkers. Am J Clin
Pathol. 2008; 129(5): 815-22.
- Baratta R., Amato S., Degano C. et al.: Adiponectin
relationship with lipid metabolism is independent of body fat mass:
evidence from both cross-sectional and intervention studies. J Clin
Endocrinol Metab 2004; 89(6): 2665-71.