Influence of smoking and body weight on adipokines in middle aged women
© I. Holzapfel Publishers 2009
Published: 7 December 2009
Quitting smoking was associated with an undesirable weight gain. Both, cigarette smoking and obesity were accompanied by subclinical systemic inflammation. This may cause unfavourable changes in (plasma) adipokine concentration. The aim of the present study was to establish the influence of moderate cigarette smoking on the concentration of the adipokines leptin and adiponectin and the pro-inflammatory factors CRP, SAA, IL-6 and TNF-α in non-obese (n = 138) and obese (n = 175) perimenopausal women of the DRECAN-2005 survey.
Among non-obese women, adiponectin was significantly lower in smokers than in non-smokers (16.88 ± 6.85 vs. 20.63 ± 10.04 μg/ml; P < 0.05). Leptin tended to lower values, too. Among obese women, none significant differences in adiponectin or leptin concentration were observed between smokers and non-smokers. In obese smokers and obese non-smokers, the adiponectin concentrations were significantly lower and the leptin concentrations were significantly higher than in non-obese non-smokers. Non-obese smokers showed significantly higher leukocyte count (6.50 ± 1.83 vs. 5.51 ± 1.31 GPT/l; P < 0.001) and serum amyloid A concentration (7.81 ± 1.25 vs. 4.22 ± 1.43 mg/l; P < 0.05) than non-obese non-smokers. There were only tendencies to higher concentration of CRP, IL-6, and TNF-α. In obese women, moderate cigarette smoking was not associated with higher leukocyte count or concentration of SAA. Among non-smokers, overweight was associated higher concentration of leptin (22.16 ± 12.16 vs. 11.49 ± 6.37 ng/ml; P < 0.001) and with significantly lower concentration of adiponectin (16.29 ± 8.01 vs. 20.77 ± 9.99 μg/ml; P < 0.001). Among smokers, overweight was associated with higher leptin concentration only (obese: 18.62 ± 13.46 vs. non-obese: 8.84 ± 4.92 ng/ml; P < 0.01).
In non-obese middle aged women, even moderate cigarette smoking adversely influences the serum concentration of adiponectin and SAA. Over-weight hides possible effects of smoking on cytokines and adipokines.
The Nurses' Health study demonstrated that among women adherence to lifestyle guidelines involving diet, exercise, and abstinence from smoking was associated with a low risk of coronary heart disease. Among middle aged women, even a moderate cigarette consumption of 1-14 cigarettes per day was shown to be one of the most important cardiovascular risk factors . Smoking is thought to be an important determinant of body weight. Cigarette smoking was associated with lower body weight, and quitting smoking typically produces weight gain. Especially perimenopausal women do not quit or start smoking to keep their body weight. Both cigarette smoking and obesity are accompanied by a low grade subclinical chronic inflammation. In obesity, this is due probably to the secretion of pro-inflammatory cytokines (TNF-α and IL-6) by adipocytes . Cigarette smoking shows an inflammatory impact on lung tissue. It promotes leukocytosis [3, 4]. Current smoking has an adverse effect on serum concentration of CRP  and it has been identified as a significant determinant of leptin and adiponectin serum concentration [6, 7]. The aim of the present study was to establish how moderate cigarette smoking influences the serum concentration of pro-inflammatory factors (SAA, IL-6, and TNF-α) and adipokines (adiponectin and leptin) in non-obese and obese women at perimenopausal age.
Materials and methods
Three hundred fourteen female participants of the 6th survey of the DRECAN-study (DRECAN-2005), aged 40-68, were included into the present study [8, 9]. The basic programme of the DRECAN studies consisted of the measurement of selected anthropometric data, personal and family history taking, and an interview-supported questionnaire according to cardiovascular risk factors and lifestyle. Fasting blood was taken in the morning between 8:00 and 10:00. Basic haematological (GenS, Beckman-Coulter, Sinsheim, Germany) and clinical chemistry analyses (MODULAR, ROCHE, Mannheim, Germany; Dx80, Beckman-Coulter, Sinsheim, Germany) were performed within 3 hours using routine methods http://www.tu-dresden.de/medikl. Numerous aliquots of serum and fluoride-EDTA-plasma were kept at -20°C for several months and analyzed serially for serum-amyloid A (SAA), hsCRP (ProSpec, Siemens, Eschborn, Germany), and TNF-α, IL-6 (Immulite, Siemens, Eschborn, Germany). Serum leptin and adiponectin concentration were measured using the LINCO Ltd. Research (St. Charles, USA) RIA methods. Among non-obese women of the DRECAN population (aged 19-70), the adiponectin concentration varied between the interquartile of 13.83-26.33 μg/ml (median: 19.04 μg/ml) and the leptin concentration between the interquartile of 7.3-13.45 ng/ml, (median: 10.7 ng/ml). Data are given as means ± SD. Statistical analyses were performed with SPPS 12.0-16.0 software package.
Characteristics of the population.
43.7 ± 12.5
53.4 ± 13.0§§
52.9 ± 11.6§§
58.5 ± 8.7§
22.23 ± 1.58
22.49 ± 1.79
28.39 ± 3.35***
28.60 ± 3.17***
Waist circumference (cm)
78.6 ± 8.0
78.4 ± 7.1
95.3 ± 11.7***
93.5 ± 9.5***
113 ± 15
127 ± 19§§§
134 ± 16§§
139 ± 18**§§§
72 ± 11
79 ± 10§§
82 ± 8§§
85 ± 9**§§§
6.50 ± 1.83***
5.51 ± 1.32
6.21 ± 1.67
6.05 ± 1.47**
7.81 ± 1.26*
4.22 ± 1.48
5.35 ± 3.24
6.74 ± 4.04*
1.20 ± 0.75
1.14 ± 1.60
1.58 ± 0.74**
1.29 ± 0.64*
5.40 ± 0.93*
5.78 ± 1.00
5.97 ± 0.64**
5.90 ± 0.89
3.19 ± 0.75*
3.56 ± 0.94
3.96 ± 0.67***
3.78 ± 0.83§
2.07 ± 0.46
2.12 ± 0.50
1.71 ± 0.44**§
1.91 ± 0.45§§§
2.14 ± 2.40
1.55 ± 1.00
1.63 ± 0.99
1.68 ± 1.11
1.62 ± 0.58
2.17 ± 4.14
3.15 ± 2.18**§§
2.98 ± 2.10**
16.88 ± 8.85*
20.76 ± 9.89
14.14 ± 7.68**
16.29 ± 8.01***
8.84 ± 4.92
11.49 ± 6.37
18.62 ± 13.46**§§
22.16 ± 12.16** §§
2.61 ± 1.83
2.45 ± 1.78
1.20 ± 0.86** §§
1.14 ± 1.42***§§
17.9% of participants (n = 56) were moderate smokers (≤ 10 cigarettes per day): 18.3% in the non-obese and 17.7% in obese women. All non-smokers were lifelong non-smokers. No significant differences in body mass index (BMI) or waist circumference were found between smokers and non-smokers: BMI in smokers 24.76 ± 4.05 kg/m2; non-smokers 25.64 ± 4.07 kg/m2; waist 86 ± 12 cm in both (Table 1). There were no significant differences in the adiponectin (smokers: 17.68 ± 6.80 μg/ml; non-smokers: 18.94 ± 9.19 μg/ml) or leptin concentration (smokers: 16.31 ± 11.84 ng/ml; non-smokers: 17.84 ± 11.24 ng/ml) between smokers and non-smokers.
Partial correlation between adipokines and markers of low grade systemic inflammation in dependency on BMI.
A/L ratio bivariate
Non-obese smokers are significantly younger than other three subgroups. The adiponectin concentration is comparable between obese and non-obese smokers (Table 1). In bivariate analysis, the leptin concentration and the A/L ratio were significantly correlated with BMI (Table 2). The leptin concentration was significantly higher and the adiponectin/leptin ratio was lower in the obese smokers than in non-obese smokers (Table 1). The concentration of CRP was comparable in obese (median 1.90 mg/l [1.35-3.52]) and non-obese smokers (median 4.80 mg/l [2.95-8.10]), whereas the concentration of SAA was significantly higher in obese smokers (median 1.30 mg/l [1.00-2.20]) than in non-obese (median 1.30 mg/l [1.00-3.52]; Mann-Whitney P < 0.05). The concentration of TNF-α (obese: median 7.8 ng/ml [4.3-9.9] vs. non-obese: median 7.9 ng/ml [6.6-12.3]) and IL-6 (obese: median 2.2 ng/ml [2.0-2.8] vs. non-obese: median 1.9 ng/ml [1.9-3.1]) were comparable in both obese and non-obese smokers.
A moderate effect of cigarette smoking on body weight is associated with an increase of the visceral obesity . Obesity promotes hypoadiponectinemia. Smoking decreases body weight. Quitters are at higher risk of weight gain. Adipose tissue has been considered an important endocrine organ that secretes biologically active substances, including adipocytokines involved in inflammation (TNF-α, IL-6, IL-10, and IL-1β), components of the acute phase response (SAA and PAI-I), and hormonal active adipokines (leptin, adiponectin, and resistin) [11, 12]. It is evident that adiponectin protects and leptin accelerates the development of atherosclerotic diseases. Despite the well-known inverse association between smoking and body weight, there have been conflicting reports on the association between smoking and adipokines, such as leptin and adiponectin.
Our hypotheses in the present study were as follows: (i) even moderate cigarette smoking decreases the serum concentration of adiponectin and has little effect on the concentration of leptin; these changes would be accompanied by signs of a low grade subclinical chronic inflammation and would be weight-dependent. We found comparable concentrations of both adipokines in smokers and non-smokers in the unselected study population. Both smoking and body weight decreased the adiponectin concentration, whereas leptin was influenced by the body weight predominantly.
Adiponectin is an adipocytokine with insulin-sensitizing, anti-inflammatory, and anti-atherogenic properties. In epidemiological studies, a paradoxical relationship between adiponectin and BMI was described . Weight loss resulted in decreasing adiponectin serum concentration [14, 15]. Adiponectin is a marker of adipocyte differentiation. Secretion of adiponectin is closely associated with the expression of the pro-inflammatory cytokines IL-6 and TNF-α in adipocytes . Adiponectin is an important player in the regulation of the inflammatory response . Cigarette smoke extract dose-dependently inhibits the differentiation of pre-adipocytes into adipocytes, which is accompanied by a blunted expression of adipocyte marker adiponectin . In men, current smoking is reflected by reduced plasma adiponectin levels [7, 20]. In the present study, we found a significantly lower adiponectin concentration in smokers, but only in the non-obese ones. In contrast to non-smokers, there was no correlation between adiponectin concentration and BMI, supporting the observation that the weight reducing effect obtained by smoking is accompanied by increasing amount of visceral fat . In the obese group, the adiponectin decreasing effect of the overweight seemed to tower above the additional effect of cigarette smoking. Recently, Sull et al  discussed that lower serum adiponectin concentrations in smokers may not be dependent on the insulin resistance status or obesity. Smoking cessation restored the adiponectin and leptin levels . Quitters' post-cessation adiponectin levels are significantly increased. Serum adiponectin levels appeared to increase considerably within two months after smoking cessation. This finding may provide further insight into the mechanisms related to the benefits of quitting smoking .
Leptin, a product of the ob gene, is an adipose tissue-derived hormone that appears to regulate both satiety and thermogenesis. It is known to play a role in food intake regulation. Circulating plasma leptin is primarily a function of adiposity . It is released from adipocyte in direct proportion to fat mass . In men, fat mass is the best predictor of serum leptin concentration. In women, percentage body fat is the best predictor of leptin . In healthy non-obese populations, fasting serum leptin concentration is significantly higher in women than in men [18, 21, 23, 24]. In 20-70 years old women without signs of an acute inflammatory process (DRECAN-2005 population), leptin concentration has positively correlated with BMI, leukocyte count, and CRP concentration even after adjustment for age or waist circumference . The concentration of leptin is significantly lower in obese middle-aged women as compared with non-obese women. Moderate cigarette smoking is associated with a tendency to lower concentration of fasting serum leptin in both obese and non-obese women. In the US population, leptin concentration is significantly associated with sex, age, BMI, fasting plasma glucose and insulin, serum triglycerides, but not with smoking, race-ethnicity, energy, and alcohol intake . There is no difference in mean leptin levels as a function of smoking status after controlling for BMI and age . In the present study population, moderate smokers with a BMI below 25 kg/m2 tended to have lower leptin concentration as compared with non-obese non-smokers. The same tendency was observed in the obese subgroup. This may reflect an improvement in leptin sensitivity. On the other hand, one may speculate that this decline becomes significantly with increasing cigarette consumption. Al Mutairi et al  described a dose-dependent effect of smoking on leptin, BMI, and the sOb-receptor. Compared with control subjects, smoking cigarettes has been associated with significantly lower serum leptin, sOb-R, and free leptin levels. Perkins found no difference in leptin concentration due to smoking status, but smoking cessation for three weeks increased leptin levels in women only . Leptin expression is increased in bronchial epithelial cells and alveolar macrophages of ex-smokers with or without severe COPD compared with never smokers. A functional leptin signaling pathway has been detected in lung epithelial cells . Smoking may modify leptin receptors and modulate leptin synthesis. The weight-lowering effect of smoking probably is not related to leptin-induced anorectic signals .
Systemic inflammation is important in the pathogenesis of cardiovascular disease. Despite the well-known inverse association between smoking and body weight, molecular mechanisms underlying this phenomenon have not been elucidated completely. Data published by Shimada et al  suggested that cigarette smoke has the potential to inhibit adipocyte differentiation via dual, independent mechanisms. Increased tissue concentration of the pro-inflammatory cytokines impaired the normal differentiation of pre-adipocytes into adipocytes. This may result in decreasing serum concentration of adiponectin . In the present study, decreasing concentration of adiponectin was not accompanied by a measurable elevation in serum levels of TNF-α, IL-6, or CRP. A pro-inflammatory effect of cigarette smoking was demonstrable in increased leukocyte count in all smokers and higher SAA concentration in non-obese smokers.
Circulating C-reactive protein (CRP), as an inflammation marker, is associated with the incidence of cardiovascular events. Increasing plasma concentration of CRP reflect an inflammatory process caused by the release of proinflammatory cytokines (IL-6 or TNF-α). CRP stimulates the classical way of the complement cascade and may induce the induction of cytokines itself. Adiponectin decreases the synthesis and secretion of CRP from endothelial cells via modulation of the AMP-kinase signaling pathway  and negatively regulates CRP expression in adipocytes . CRP seems to be a useful biomarker for an obesity-caused subclinical inflammation . In men, serum concentration of CRP correlates with WHR . Weight loss is associated with a decline in serum concentration of CRP . Beside the liver, macrophages, smooth muscle cells and adipocytes produce CRP. In adipose tissue, an inverse relationship between CRP and adiponectin mRNA has been described . In Japanese men, both leptin (negatively) and adiponectin (positively) are independently associated with CRP concentration . Leptin is more strongly related to CRP levels than adiponectin, especially among obese men . Among women of the DRECAN-05 population, leptin concentration highly correlated with CRP and BMI . In the present study, a correlation with CRP could be confirmed in non-smokers only. There exists a strong inverse correlation between CRP and adiponectin mRNA . In healthy obese women or in non-diabetic women, adiponectin serum concentration correlates with CRP [32, 33]. In a subgroup of non-smokers of the present study, the correlation of adiponectin with CRP was weak and it was not demonstrable in smokers. Maybe, this was due to different menopausal status and use of hormone replacements. Hormone replacement therapy seems to increase the serum concentration of CRP [5, 34]. Postmenopausal women in the lowest quartile of visceral fat and not on HRT show a significantly lower CRP than women in the highest quartile of visceral fat independently of HRT use .
Diabetes and metabolic syndrome are associated with increased low grade inflammation . IL-6 acts on hepatocytes inducing the acute phase reaction/reactants. Among non-smokers, the plasma level of IL-6 correlates with absolute and relative fat mass, fasting insulin, and blood pressure. These effects are dependent on gender and current smoking status [8, 36]. Among women, the correlation of IL-6 with fasting insulin could not be observed. Adiponectin is able to inhibit the activation of NF-κB in macrophages and endothelial cells. Hypoadiponectinemia increases concentrations of IL-6 and IL-8 in plasma [17, 37]. In the present study, after adjustment for BMI, we found only a weak correlation of adiponectin and the A/L ratio with IL-6 in non-smokers.
Tumor necrosis factor alpha (TNF-α) is produced mainly by macrophages in response to inflammation or cancer and by adipocytes [38, 39]. In adipocytes, pro-inflammatory cytokines such as TNF-α downregulate the expression of adiponectin and upregulate the production of leptin . Adiponectin again inversely regulates the TNF-α expression in the adipose tissue . It is still unclear whether an increased TNF-α production in the adipose tissue is reflected by increased serum concentration . Moderate cigarette consumption in middle aged women was not reflected by increased serum concentration of TNF-α or significant correlation between adiponectin and TNF-α in smokers.
Conflicts of interest
There are no personal potential financial conflicts of interest declared by the authors, according to employment, honoraria, grants received, consultancies, patents received, or stock ownerships, in relation to this article.
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