18.02.2013 Views

Tobacco and Public Health - TCSC Indonesia

Tobacco and Public Health - TCSC Indonesia

Tobacco and Public Health - TCSC Indonesia

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

536<br />

ENDOMETRIAL CANCER<br />

results to those that did not, suggesting that BMI is not a strong confounding variable<br />

in this association.<br />

Two studies examined the association between cigarette smoking <strong>and</strong> blood<br />

estrogen levels after r<strong>and</strong>omization of women to groups receiving either estradiol or<br />

placebo (Table 31.5) (Jensen <strong>and</strong> Christiansen 1988; Cassidenti et al. 1990). In a<br />

small study of 25 postmenopausal women (Cassidenti et al. 1990), unbound estradiol<br />

was significantly lower among smokers than nonsmokers both at baseline <strong>and</strong><br />

shortly after taking micronized estradiol orally. No important differences were<br />

observed between smokers <strong>and</strong> nonsmokers in serum levels of either estrone or bound<br />

estradiol. In contrast, a study in which 110 postmenopausal women were r<strong>and</strong>omized<br />

to take hormones (either orally or percutaneously) or a placebo (Jensen <strong>and</strong><br />

Christiansen 1988) found that smokers had lower levels of both estrone <strong>and</strong> bound<br />

estradiol than nonsmokers after oral (but not percutaneous) hormone treatment for<br />

at least one year (levels of free estrogens were not examined). These results indicate<br />

that smoking might affect the absorption or metabolism of hormones used in<br />

replacement therapy.<br />

Smoking <strong>and</strong> blood sex-hormone binding globulin<br />

(SHBG) levels<br />

Of the five studies that have examined the association between cigarette smoking <strong>and</strong><br />

serum (Lapidus et al. 1986; Cassidenti et al. 1992; Law et al. 1997) or plasma (Khaw<br />

et al. 1988; Longcope <strong>and</strong> Johnston 1988) SHBG, none found any clear association.<br />

However, one of these studies (Khaw et al. 1988) found an inverse association between<br />

smoking <strong>and</strong> the ratio of bound estradiol to SHBG, a measure of estrogen activity.<br />

In this context, it is interesting to note that Cassidenti et al. (1990) found unbound<br />

(but not SHBG-bound) estradiol significantly lower among smokers than nonsmokers<br />

both at baseline <strong>and</strong> after taking oral estradiol, suggesting an increased SHBG-binding<br />

capacity in the women who smoked.<br />

Smoking <strong>and</strong> blood <strong>and</strong>rogen levels<br />

In postmenopausal women, <strong>and</strong>rogens are the major source of estrone, converted<br />

through an aromatization process in fat deposits. Thus, adiposity is positively correlated<br />

with estrogen levels in postmenopausal women. Of the nine studies that examined<br />

blood levels of <strong>and</strong>rostenedione in smokers (Friedman et al. 1987; Khaw et al. 1988;<br />

Longcope <strong>and</strong> Johnston 1988; Cauley et al. 1989; Slemenda et al. 1989; Schlemmer<br />

et al. 1990; Cassidenti et al. 1992; Austin et al. 1993; Law et al. 1997), all found higher<br />

circulating levels among current than never or former smokers (Table 31.5). However,<br />

these same studies did not show clear variation in blood estrone levels by smoking<br />

status, perhaps suggesting a reduced conversion of <strong>and</strong>rostenedione to estrone among<br />

smokers. Of the five studies that have examined cigarette smoking <strong>and</strong> DHEAS levels,<br />

three (Friedman et al. 1987; Khaw et al. 1988; Cassidenti et al. 1992) found increased

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!