S. J. Nyante, B. I. Graubard, Y. Li, G. M. McQuillan, E. A. Platz, S. Rohrmann, G. Bradwin, K. A. McGlynn
{"title":"美国男性性激素浓度趋势:1988-1991年至1999-2004年","authors":"S. J. Nyante, B. I. Graubard, Y. Li, G. M. McQuillan, E. A. Platz, S. Rohrmann, G. Bradwin, K. A. McGlynn","doi":"10.1111/j.1365-2605.2011.01230.x","DOIUrl":null,"url":null,"abstract":"<p>Previous studies suggest that male testosterone concentrations have declined over time. To explore this in a large US population, we examined testosterone and free testosterone concentrations in National Health and Nutrition Examination Surveys (NHANES) from 1988–1991 and 1999–2004. We also examined sex hormone-binding globulin (SHBG), estradiol, and androstanediol glucuronide (3α-diol-G) over the same period. Non-Hispanic white, non-Hispanic black, and Mexican-American men from 1988–1991 and 1999–2004 NHANES surveys who were ≥20 years old and had serum from morning blood draws were included in this analysis (1988–1991: <i>N</i> = 1,413; 1999–2004: <i>N</i> = 902). Testosterone, estradiol and SHBG were measured by competitive electrochemiluminescence immunoassays and 3α-diol-G was measured by enzyme immunoassay. Free testosterone was calculated using testosterone and SHBG values. Adjusted mean hormone concentrations were estimated using linear regression, accounting for NHANES sampling weights and design, age, race/ethnicity, body mass index, waist circumference, alcohol use and smoking. Differences in adjusted mean concentrations (Δ) and two-sided <i>p</i>-values were calculated; <i>p</i> < 0.05 was statistically significant. Overall, 3α-diol-G and estradiol declined between 1988–1991 and 1999–2004, but there was little change in testosterone, free testosterone, or SHBG (Δ: 3α-diol-G = −1.83 ng/mL, <i>p</i> < 0.01; estradiol = −6.07 pg/mL, <i>p</i> < 0.01; testosterone = −0.03 ng/mL, <i>p</i> = 0.75; free testosterone = −0.001 ng/mL, <i>p</i> = 0.67; SHBG = −1.17 nmol/L, <i>p</i> = 0.19). Stratification by age and race revealed that SHBG and 3α-diol-G declined among whites 20–44 years old (Δ: SHBG = −5.14 nmol/L, <i>p</i> < 0.01; 3α-diol-G = −2.89 ng/mL, <i>p</i> < 0.01) and free testosterone increased among blacks 20–44 years old (Δ: 0.014 ng/mL, <i>p</i> = 0.03). Estradiol declined among all ages of whites and Mexican-Americans. In conclusion, there was no evidence for testosterone decline between 1988–1991 and 1999–2004 in the US general population. Subgroup analyses suggest that SHBG and 3α-diol-G declined in young white men, estradiol declined in white and Mexican-American men, and free testosterone increased in young black men. These changes may be related to the increasing prevalence of reproductive disorders in young men.</p>","PeriodicalId":13890,"journal":{"name":"International journal of andrology","volume":"35 3","pages":"456-466"},"PeriodicalIF":0.0000,"publicationDate":"2011-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/j.1365-2605.2011.01230.x","citationCount":"39","resultStr":"{\"title\":\"Trends in sex hormone concentrations in US males: 1988–1991 to 1999–2004\",\"authors\":\"S. J. Nyante, B. I. Graubard, Y. Li, G. M. McQuillan, E. A. Platz, S. Rohrmann, G. Bradwin, K. A. McGlynn\",\"doi\":\"10.1111/j.1365-2605.2011.01230.x\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Previous studies suggest that male testosterone concentrations have declined over time. To explore this in a large US population, we examined testosterone and free testosterone concentrations in National Health and Nutrition Examination Surveys (NHANES) from 1988–1991 and 1999–2004. We also examined sex hormone-binding globulin (SHBG), estradiol, and androstanediol glucuronide (3α-diol-G) over the same period. Non-Hispanic white, non-Hispanic black, and Mexican-American men from 1988–1991 and 1999–2004 NHANES surveys who were ≥20 years old and had serum from morning blood draws were included in this analysis (1988–1991: <i>N</i> = 1,413; 1999–2004: <i>N</i> = 902). Testosterone, estradiol and SHBG were measured by competitive electrochemiluminescence immunoassays and 3α-diol-G was measured by enzyme immunoassay. Free testosterone was calculated using testosterone and SHBG values. Adjusted mean hormone concentrations were estimated using linear regression, accounting for NHANES sampling weights and design, age, race/ethnicity, body mass index, waist circumference, alcohol use and smoking. Differences in adjusted mean concentrations (Δ) and two-sided <i>p</i>-values were calculated; <i>p</i> < 0.05 was statistically significant. Overall, 3α-diol-G and estradiol declined between 1988–1991 and 1999–2004, but there was little change in testosterone, free testosterone, or SHBG (Δ: 3α-diol-G = −1.83 ng/mL, <i>p</i> < 0.01; estradiol = −6.07 pg/mL, <i>p</i> < 0.01; testosterone = −0.03 ng/mL, <i>p</i> = 0.75; free testosterone = −0.001 ng/mL, <i>p</i> = 0.67; SHBG = −1.17 nmol/L, <i>p</i> = 0.19). Stratification by age and race revealed that SHBG and 3α-diol-G declined among whites 20–44 years old (Δ: SHBG = −5.14 nmol/L, <i>p</i> < 0.01; 3α-diol-G = −2.89 ng/mL, <i>p</i> < 0.01) and free testosterone increased among blacks 20–44 years old (Δ: 0.014 ng/mL, <i>p</i> = 0.03). Estradiol declined among all ages of whites and Mexican-Americans. In conclusion, there was no evidence for testosterone decline between 1988–1991 and 1999–2004 in the US general population. Subgroup analyses suggest that SHBG and 3α-diol-G declined in young white men, estradiol declined in white and Mexican-American men, and free testosterone increased in young black men. These changes may be related to the increasing prevalence of reproductive disorders in young men.</p>\",\"PeriodicalId\":13890,\"journal\":{\"name\":\"International journal of andrology\",\"volume\":\"35 3\",\"pages\":\"456-466\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2011-12-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1111/j.1365-2605.2011.01230.x\",\"citationCount\":\"39\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International journal of andrology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/j.1365-2605.2011.01230.x\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International journal of andrology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/j.1365-2605.2011.01230.x","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 39
摘要
先前的研究表明,男性睾酮浓度随着时间的推移而下降。为了在大量美国人群中探索这一点,我们在1988-1991年和1999-2004年的国家健康和营养检查调查(NHANES)中检测了睾酮和游离睾酮浓度。我们还在同一时期检测了性激素结合球蛋白(SHBG)、雌二醇和雄甾二醇葡萄糖醛酸盐(3α-二醇- g)。本分析包括1988-1991年和1999-2004年NHANES调查中年龄≥20岁并有晨采血清的非西班牙裔白人、非西班牙裔黑人和墨西哥裔美国男性(1988-1991年:N = 1413;1999-2004年:n = 902)。采用竞争电化学发光免疫法测定睾酮、雌二醇和SHBG,采用酶免疫法测定3α-二醇- g。利用睾酮和SHBG值计算游离睾酮。考虑到NHANES抽样权重和设计、年龄、种族/民族、体重指数、腰围、饮酒和吸烟,使用线性回归估计调整后的平均激素浓度。计算调整后的平均浓度(Δ)和双侧p值的差异;P < 0.05差异有统计学意义。总体而言,3α-二醇- g和雌二醇在1988-1991年和1999-2004年期间下降,但睾酮、游离睾酮和SHBG变化不大(Δ: 3α-二醇- g = - 1.83 ng/mL, p < 0.01;雌二醇= - 6.07 pg/mL, p < 0.01;睾酮= - 0.03 ng/mL, p = 0.75;游离睾酮=−0.001 ng/mL, p = 0.67;SHBG = - 1.17 nmol/L, p = 0.19)。年龄和种族分层显示,20-44岁白人SHBG和3α-二醇- g下降(Δ: SHBG = - 5.14 nmol/L, p < 0.01;3α-二醇- g = - 2.89 ng/mL, p < 0.01), 20 ~ 44岁黑人游离睾酮增加(Δ: 0.014 ng/mL, p = 0.03)。雌二醇在所有年龄段的白人和墨西哥裔美国人中都有所下降。总之,在1988-1991年和1999-2004年期间,美国普通人群中没有睾丸激素下降的证据。亚组分析表明,年轻白人男性SHBG和3α-diol-G下降,白人和墨西哥裔美国男性雌二醇下降,年轻黑人男性游离睾酮升高。这些变化可能与年轻男性中生殖障碍的患病率上升有关。
Trends in sex hormone concentrations in US males: 1988–1991 to 1999–2004
Previous studies suggest that male testosterone concentrations have declined over time. To explore this in a large US population, we examined testosterone and free testosterone concentrations in National Health and Nutrition Examination Surveys (NHANES) from 1988–1991 and 1999–2004. We also examined sex hormone-binding globulin (SHBG), estradiol, and androstanediol glucuronide (3α-diol-G) over the same period. Non-Hispanic white, non-Hispanic black, and Mexican-American men from 1988–1991 and 1999–2004 NHANES surveys who were ≥20 years old and had serum from morning blood draws were included in this analysis (1988–1991: N = 1,413; 1999–2004: N = 902). Testosterone, estradiol and SHBG were measured by competitive electrochemiluminescence immunoassays and 3α-diol-G was measured by enzyme immunoassay. Free testosterone was calculated using testosterone and SHBG values. Adjusted mean hormone concentrations were estimated using linear regression, accounting for NHANES sampling weights and design, age, race/ethnicity, body mass index, waist circumference, alcohol use and smoking. Differences in adjusted mean concentrations (Δ) and two-sided p-values were calculated; p < 0.05 was statistically significant. Overall, 3α-diol-G and estradiol declined between 1988–1991 and 1999–2004, but there was little change in testosterone, free testosterone, or SHBG (Δ: 3α-diol-G = −1.83 ng/mL, p < 0.01; estradiol = −6.07 pg/mL, p < 0.01; testosterone = −0.03 ng/mL, p = 0.75; free testosterone = −0.001 ng/mL, p = 0.67; SHBG = −1.17 nmol/L, p = 0.19). Stratification by age and race revealed that SHBG and 3α-diol-G declined among whites 20–44 years old (Δ: SHBG = −5.14 nmol/L, p < 0.01; 3α-diol-G = −2.89 ng/mL, p < 0.01) and free testosterone increased among blacks 20–44 years old (Δ: 0.014 ng/mL, p = 0.03). Estradiol declined among all ages of whites and Mexican-Americans. In conclusion, there was no evidence for testosterone decline between 1988–1991 and 1999–2004 in the US general population. Subgroup analyses suggest that SHBG and 3α-diol-G declined in young white men, estradiol declined in white and Mexican-American men, and free testosterone increased in young black men. These changes may be related to the increasing prevalence of reproductive disorders in young men.