The dopamine transporter gene (DAT1) codes for a dopamine transporter protein, which limits the level and duration of dopamine receptor activation. The DAT1 gene is a strong candidate gene for reward-seeking behavior. This article reports compelling evidence for the association between the 40 bp variable number of tandem repeats in the DAT1 gene and the self-reported number of sexual partners among young adults in the United States using the sibling subsample of more than 2500 individuals who participated in the National Longitudinal Study of Adolescent Health. We performed tests of genotype–gender interaction as well as analyses stratified by gender. Among the males, possessing one or two alleles of the 10 repeat is associated with an 80–100% increase (P<0.0001, 2df) in the number of sexual partners as compared with the homozygotes for the 9 repeat. The association holds in race/ethnicity-stratified analyses, in Allison's procedure that tests population stratification, and in within-family fixed-effects models. Covariate adjustment for a standard set of socioeconomic factors including religiosity, family structure, parental education, marital and cohabitation history, and neighborhood poverty did not attenuate these associations. Discussion is provided why this finding is absent among females.
Although many young adults delay marriage or other forms of long-term commitment, they have more sexual partners than any other age group.1, 2 The number of sexual partners youth have is an important indicator of the risk of contracting a sexually transmitted disease (STD), including HIV.3, 4 Of estimated 12 million of new STD infections that occur each year in the US, three million occur among people younger than 20, and another four million occur among those aged between 20 and 25.5
Both animal and human studies have demonstrated a genetic basis for sexual behavior. A twin study based on 1600 female twin pairs reported that approximately 40% of the variance in the self-reported number of sexual partners can be attributed to genetic factors.6 Studies on humans indicate that the stimulation of dopamine receptors would enhance male sexual behavior and that the inhibition of them would impair male sexual behavior.7 Pharmacological experiments using animal models have also shown that increased dopamine activity boosts male sexual activity.7
The soluble carrier family six dopamine transporter member three gene (DAT, locus symbol: SLC6A3) codes for a dopamine transporter protein (DAT), which limits the level and duration of dopamine receptor activation.8 The mouse model of dopamine transporter gene knockout established not only the central importance of dopamine transporter in controlling synaptic dopamine levels, but also its role as an obligatory target for the behavioral and biochemical action of amphetamine and cocaine.9 Vandenbergh et al10 identified several polymorphisms in DAT1, including a polymorphic 40 bp repeat in the transcribed portion of the gene, which is most commonly observed repeat 9 (DAT1*9R) to 10 times (DAT1*10R). One study found that humans homozygous for the 10R allele exhibited significantly lower dopamine transporter binding than carriers of the 9R allele,11 although the findings from another study are inconsistent.12
Intense interest has been directed at understanding the role of the dopamine transporter gene in the neurotransmission process because of its involvement in several behaviors. A number of studies have demonstrated an association between the 10R allele in the DAT1 gene and attention deficit hyperactivity disorder.13, 14, 15, 16, 17 The DAT1*9R allele was reported to be associated with both a lower score in novelty seeking and a greater success in smoking cessation,18 cocaine-induced paranoia,19 and an increased risk for delirium and seizures during withdrawal in alcoholics.20, 21 Although no study seems to have focused on the DAT1 variants and number of sexual partners, the link is plausible because of the central role of dopamine in motor activity and reward-seeking behavior.
Gender is a crucial factor to be considered in studies of number of sexual partners. Males of most mammalian species show a strong desire towards variety in sexual partners. In the laboratory, this phenomenon has been referred to as the ‘Coolidge effect’.22, 23, 24 It was first observed among rats. The same effect is even more striking in farm animals such as sheep and cattle.25 Studies based on self-reports among human subjects found that partner variety is of greater interest to male adolescents,26 male college students27 and male adults28, 29, 30, 31, 32 than their female counterparts.
Two broad theoretical approaches have been developed to explain the gender differences in number of sexual partners or, more generally, reproductive strategies: the evolutionary theory and the social control of human sexuality. The evolutionary theory argues that the differences in the relative costs and benefits of sexual behaviors between the two genders over the evolutionary process have produced the gender differences in mating predispositions.33, 34, 35, 36, 37, 38 For females, every copulation might have led to conception, followed by lengthy periods of child-bearing and child-rearing; having more sexual partners did not increase female fitness. Thus, females who selected fewer sexual partners with ability and willingness to contribute parental resources tended to place successfully offspring in succeeding generations. As a result, female traits related to mating choosiness were selected by evolution and were passed onto the present human populations. In contrast, males could increase their reproductive success by increasing the number of sexual partners because they were not contributing similar resources and time.
Social theories have emphasized social regulation of human sexuality as a source for gender differences in sexual behavior.39, 40 Religion and family have historically been important institutions for regulating sexuality in Western society. Social theories argue that the gender differences are at least partially due to double sexual standards because men traditionally enjoy more power than women in virtually all the major institutions: politics, religion, economics, and family. Male sexual activity is tolerated and even encouraged, whereas the female sexual activity is more controlled and subject to censure of violation of norms. Because of the changes in gender role attitudes and the general understanding of male and female sexuality in recent decades, sexual standards have become more permissive and more egalitarian between the two genders.
The present study has three objectives. The first is to investigate the association between the 40 bp variable number of tandem repeats (VNTR) in the DAT1 gene and the self-reported number of sexual partners among young adults using the DNA sample of about 2500 individuals in the National Longitudinal Study of Adolescent Health (Add Health). The second objective aims at testing the interaction between the DAT1 variants and gender for the number of sexual partners. Lastly, we re-estimate the association after taking into account of a social science model of sexual behavior including religiosity, family structure, parental education, marital and cohabitation history, neighborhood poverty, and health behavior such as alcohol use and illegal drug use.
Materials and methods
The data source for our analysis is the sibling subsample of about 2500 participants in the Add Health, a nationally representative sample of more than 20 000 adolescents in grades 7–12 in 1994–1995 in the United States.41 Add Health is longitudinal; the respondents have since been followed by two additional in-home interviews in 1995–1996 (Wave II) and 2002 (Wave III).
In Wave III in 2002, DNA samples were collected from a subset of the Add Health sample. The subset consists of a total of 2597 participants including MZ twins (186 pairs), same-sex DZ twins (136 pairs), opposite-sex DZ twins (103 pairs), full biological siblings (569 pairs), and singletons.
Number of sexual partners
At Wave III, the respondents aged 19–26 were asked the question: ‘With how many partners have you ever had vaginal intercourse, even if only once?’ To protect confidentiality, reduce nonresponses and increase reporting accuracy, this section of the interview was self-administered by audio-CASI (computer-assisted self-interview). The sensitive question was read to respondents by means of audio headphones. Respondents were given instructions on how to complete their answers on the computer. The technique has been shown to reduce the disparity between men and women in the number of sex partners reported.42 Table 1 gives the mean reported number of sexual partners and standard deviation by ethnicity, age group, and gender.
As in every other survey on number of sexual partners,43 the number of female partners reported by males exceeds the number of male partners reported by females in Add Health. The overall male-to-female ratio in Add Health is about 1.3. Because a heterosexual intercourse involves a male and a female, in a closed population, the total number of copulations for males must be the same as those for females; the total number of sexual partners for males must also be the same as those for females. Two hypotheses have been proposed to explain the higher reported male-to-female ratio: (1) Males over-report and (2) most females have fewer partners than most males, but a few females have a very large number of partners. Brewer et al44 tested the second hypothesis using data from national sex studies of prostitutes and their clients in the United States. They found an under-representation of prostitute women in these national surveys. Once the under-representation and their large numbers of sexual partners are factored in, the male–female disparity disappears.
DNA preparation and genotyping
At Wave III in 2002, in collaboration with the Institute for Behavioral Genetics in Boulder, CO, Add Health collected, extracted, and quantified DNA samples from the sibling subsample. Genomic DNA was isolated from buccal cells using a modification of published methods.45, 46, 47, 48 All the methods employed Applied Biosystems instruments and reagents. Microsatellite and VNTR polymorphisms were performed using fluorescent primers that were analyzed on an ABI capillary electrophoresis instrument. Single nucleotide polymorphisms were analyzed using an ABI Sequence Detection System and 5′-nuclease (Taqman®) methodology.
A 40 bp VNTR polymorphism in the 3′ untranslated region of the DAT1 gene has been genotyped with a modified method of Vandenbergh et al.49 The VNTR ranges from 3 to 11 copies with the 9-repeat (9R) and 10-repeat (10R) polymorphisms being the two most common alleles in Caucasian, Hispanic and African-American populations.50 In our analysis sample, the 9R and 10R account for about 21 and 76% of all alleles, respectively; 35, 59, and 0.048% of the respondents possess one 10R, two 10Rs, and two 9Rs, respectively (Table 2). The variation across ethnic groups appears to be moderate with the 10R allele accounts for 80, 86, 80, and 90% of all alleles in whites, blacks, Hispanics, Asians, respectively. A series of χ2 tests for the polymorphism and for each self-reported ethnic group (European, African-American, Hispanic, and Asian) reveals no deviation from the Hardy–Weinberg equilibrium.
Table 2 also provides the descriptive statistics for socioeconomic and other nongenetic factors used in the analysis. Church attendance measures attendance frequency with categories of never, less than once/month, less than weekly, and weekly or more. Family structure is a variable of four categories: two-biological-parent families, single-parent families, step-parent families, and other types of families including families with adopted and foster children. One's marital and cohabitation history may be related to the number of sexual partners. Our marriage/cohabitation includes categories of being single, having cohabited and have been married, having been only married, and having only cohabited. Parental education also has four categories: less than high school, high school graduation, some college, and at least a college degree. Add Health measured the level of education from both the mother and the father of a respondent. We used the higher of the two when both were available. Poverty at the neighborhood level is measured by the proportion of families living below the official poverty line in a Census block group, which is the smallest geographic area for which the Census Bureau publishes sample data. In 1990, block groups averaged 452 housing units or 1100 individuals. The block groups are divided into low-poverty, median-poverty, and high-poverty categories. The two cutoff points for the three categories are 11.6 (the median proportion of families in a block group living below the poverty line) and 23.9% (the 75th percentile of the proportion of families in a block group living below the poverty line).
To test the association between the DAT1 variants and the number of sexual partners, a three-step analytical strategy was adopted. The first step was an exploratory data analysis that compares the mean count of partners across genotypes, stratified by gender and age group. In the second step, we estimated a number of generalized estimating equations (GEE) Poisson regression models51 that adjust for the correlation among siblings in the data and allow covariate adjustment for factors such as gender, race/ethnicity, and a set of social environmental factors. The third step addresses potential bias from population stratification.
The rest of this section elaborates on the second and third steps. Step 2 uses the Poisson regression model,
where E(Yij∣xij) is the expected number of partners for individual i in sibling cluster j given the individual's characteristics xij and DAT1ij represents the genetic variants for the individual. The exposure was explicitly adjusted by age (not shown in equation; see Table 4). To account for the dependence among the siblings in the Add Health data, we estimated the model using the GEE,51 which has long been established in the statistical literature as a standard approach for addressing correlated data. The GEE models were implemented using SAS. In addition, we performed gender-stratified analysis, in which we estimated Equation (1) twice, each time using only the male or female sample.
We used four strategies to address the potential impact of population structure. First, we adjusted for self-reported race/ethnicity in all regression analysis so that the comparisons across genotypes are made after adjusting for any main effect of race/ethnicity. Second, we estimated the genotype effect in a white male sample and a black male sample separately. As a third strategy, we applied the Allison et al's52 procedure to test for possible population stratification. The procedure is based on the reasoning that the probabilities of genotypes of siblings depended entirely on parental genotypes and that controlling for the genotype effects of sibship would be equivalent to controlling for parental genotypes. This model could be considered as a special case of the mixed model.53, 54 Our last strategy is a stringent within-family fixed-effect model that has been used widely to account for unobserved effects at the family level.55
Genotypic mean count by gender and age
Table 3 shows the number of sexual partners by genotype, gender, and age. Among the males, the 10R appears to be associated with higher number of sexual partners. In the younger group of 18–22 years, possessing one or two copies of 10R approximately doubles the number of partners. In the older group of 23–26 years, possessing one or two copies of 10R increases the number of partners from about 4–7. Age is positively related to the number of partners; but there does not seem be an interaction between age and the effect of the DAT1 variants, that is, the effect of DAT1 does not seem to vary across the life stages of adolescence and young adulthood. Among the females, the 10R allele does not seem to be associated with higher number of sexual partners. This is the case in both age groups, suggesting an interaction between DAT1 and gender. Because of the sibling clustering in the data, standard significance tests are not valid for these comparisons. The next section presents significance tests for the main effects of DAT1 and the interactive effects of DAT1 and gender obtained from the GEE regression models.
Table 4 reports the results from the GEE Poisson models that adjust for the correlation among the siblings in our sample. Using the combined sample of males and females, Model 1 estimates the main effects of the DAT1 polymorphism and gender after controlling for race/ethnicity. According to Model 1, those with the DAT1*10R/10R genotype reported 32% (P=0.038, CI (1.02, 1.72)) more sexual partners than the DAT1*9R/9R genotypes; those with the DAT1*10R/9R genotype reported 39% (P=0.018, CI (1.06, 1.84)) more partners. These results apply to both males and females. The model has also adjusted for age groups.
We also estimated a gene–gender interaction model (data not shown) that adds to the first model the interaction terms between genotype and gender. The model indicates that the association of the 10R allele of DAT1 only applies to males. Among the males, the 10R/10R genotype raises the number of partners by 93% relative to the 9R/9R genotype; similarly, the 10R/9R raises the number of partners by 83%. The genotype effect does not exist among the females. The gene–gender interaction model is highly significant over Model 1 by the likelihood ratio test (χ2=37 with 3 df).
Table 4 also presents the results of the gene–gender interaction estimated by stratifying the sample by gender. We estimated two such models one for males and one for females without adjusting for social control variables (data not shown). In the male model, the DAT1*10R/10R genotype is associated with a 100% (P=0.001, CI (1.32, 3.03)) increase in the reported number of sexual partners relative to the DAT1*9R/9R genotype; the corresponding increase for the DAT1*10R/9R genotype is 88% (P=0.005, CI (1.21, 2.92)). In the female model, the genotypes do not seem to be related to the number of partners (P=0.53 and 0.57, respectively). The second and third models in Table 4 re-estimated these results after including a set of socioeconomic factors: church attendance, family structure, parental education, marital and cohabitation history, and neighborhood poverty. The association between the genotype and the number of partners continues to be absent among the females. Among the males, the two genotypes of 10R/10R and 10R/9R raise the number of partners by 90% (P=0.0002, CI (1.36, 2.66)) and 79% (P=0.0015, CI(1.25, 2.55)), respectively.
The effects of socioeconomic factors are generally consistent with expectations. Having a step-parent or single-parent relative to having two-biological parents, having a cohabitation history, and especially attending church service less than weekly relative to weekly or more tend to be associated with a higher number of sexual partners. Having some college education (but not having at least a college degree) relative to just a high school education is associated with a higher number of partners.
Our final model – the male model with the social controls in Table 4 – was tested for robustness through the addition of illegal drug use and alcohol use. Previous work reported a substantial correlation between number of sexual partners and risky behaviors.57 Both illegal drug use (any illegal drug use at Wave III) and alcohol use (frequency over past year at Wave III) are positively and significantly related to number of partners; however, our key findings have remained unchanged with the adjustment of the two risky behaviors (data not shown). For example, with the adjustment, the exp(β)s for 10R/10R and 10R/9R are 1.87 (P=0.0001) and 1.76 (P=0.0008), respectively, as compared with 1.89 (P=0.0002) and 1.78 (P=0.001), respectively, estimated without the adjustment.
To address the potential biases from population stratification, we carried out the four strategies described earlier. First, race/ethnicity was included as a control in all regression models estimated (Table 4). Second, we have further stratified our male sample by race/ethnicity. Our main results hold within both the white and black samples; the estimated effect sizes of DAT1 have remained similar to those based on the ethnicity-combined models, but the P-values are smaller as expected (Figure 1). We carried out Allison's procedure52 that includes three random parameters: one random effect at the sibling level, a second random effect at the individual level, and a third random parameter designed to capture the interaction between the genotype across sibling clusters and the observed DAT1 variants. We estimated this model using the mixed or multilevel model because the Poisson random effect model with more than one random effect depends on approximations and often yields highly biased results.58 The included random interaction term from the Allison's procedure is highly significant with P<0.0001. The DAT1*Any10R is associated with 2.6 more sexual partners (P=0.0016, CI (1.03, 4.14)) than the 9R/9R genotype (data not shown), which is consistent with the results from the Poisson models in Table 4. We performed the within-family fixed-effect linear regression using 237 pairs of male DZ twins and full biological siblings in the DNA sample. Compared with 9R/9R, the 10R/10R and 10R/9R genotypes reported 5.69 (P=0.049) and 5.05 (P=0.066) more sexual partners, respectively.
Figure 1 summarizes the main findings by graphing the ratios of number of sexual partners by genotype. The three sets of bars are based upon the combined genetic and social-science model of all ethnicities, the white sample and the black sample. The P-values are based upon a likelihood ratio test that compares the model with genotype and the model without genotype using two degrees of freedom. The DAT1*9R/9R is the reference category and its value is set as one. The association between DAT1 and number of sexual partners is evident in each of the three samples.
Very few studies seem to have examined the link between the genetic variants in the dopaminergic system and human sexual behavior. Miller et al59 reported a positive association between the presence of the 2 allele of DRD2 and age at first sex in a sample of 414 middle-class non-Hispanic European American men and women. Two recent studies, also based on Add Health, examined age at first sex and self-reported number of sexual partners over the past 12 months, respectively.60, 61 The former found a link with a DRD4 variant in the white, Hispanic and Asian samples. The latter reported an association with a DRD2 variant and a 5HTT-religiosity interaction. The DAT1 gene was not related to number of sex partners over the past 12 months in the latter study. The present study reported an association between the 40 bp VNTR in the DAT1 gene and lifetime number of sexual partners. It is likely that the short- and long-term numbers of sexual partners are not subject to the same set of genetic and environmental factors. The model with social control for the males in Table 4 in the present study yielded an R2 of 0.126 indicating that a large portion of the variance remains unexplained. Some other polymorphisms within DAT1 and other genes may also contribute to our lifetime measure of number of partners.
Evidence for the differences between males and females in sexual behavior was reported from animal studies. The neurotransmitter dopamine has been shown to facilitate male sexual behavior in all investigated species including rodents and humans.7 Melis and Argiolas'62 findings suggest a major role for dopaminergic receptors in both the preparatory and consummatory phase of male sexual behavior, whereas their role in female sexual behavior is less conclusive. Hull et al63 discussed three mechanisms through which males sexual behavior is affected by dopamine among rats: dopamine increases male sexual arousal and courtship behavior, enhances the motor acts of mounting behavior, and facilitates genital response to stimulation.
We researched for evidence that may explain the sex differences in our findings via the twin and full-sib data in Add Health and biometrical methods. Table 5 gives the twin and sibling intraclass correlations and number of pairs by gender and type of sibling pairs using the mixed models.56 Heritability of number of sex partners was estimated to be 0.50 for females and 0.38 for males. The estimates were obtained after controlling for age and ethnicity. Partly because the numbers of pairs available were moderate, we were unable to show that the two estimates are statistically different from one another. Overall, the biometrical data do not offer a clear answer to the question of whether a sex-specific genetic component is present, which is suggested by the analysis of DAT1 variants.
We briefly outlined two theoretical perspectives earlier in this article to interpret the gene–gender interaction or the absence of the effect of DAT1 among females. The evolutionary argument is based on the vast physiological differences in the reproductive system between males and females. Because of the differences, partner variety only increases the male fitness and not the female one. The argument hypothesizes that the evolutionary process has selected gender-specific physiological basis for partner variety. The male-to-female ratio of self-reported partners in our sample is consistent with the evolutionary argument; however, the DAT1 gene is unlikely to be part of the gender-specific basis because of its presence in both genders. Nevertheless, it is possible that the gender-specific system interacts with DAT1 and suppresses its ramifications for partner variety among females. The perspective of social control of human sexuality predicts a stronger societal control for females than males. The stronger social regulation of female sexuality could lessen or completely suppress the potential impact of the DAT1 gene on partner variety. Our findings of gene–gender interaction are thus consistent with both the evolutionary and the social control arguments, but this study is unable to produce evidence to disprove one in favor of the other.
A gene–gender interaction shares similarities with a gene–environment interaction. A gene–gender interaction can be a gene–environment interaction as suggested by the social control argument, a gene–gene interaction as suggested by the evolutionary argument or simultaneously a gene–environment interaction and a gene–gene interaction.
The DAT1 gene is unlikely to be a ‘sex’ gene itself. As suggested earlier in this article, the more likely scenario is that the gene is associated with a predisposition for a number of related behaviors, of which sexual partner variety is one. The gene may have a moderate effect on certain behaviors and may interact with environment to exert such an effect, that is, whether the genetic predisposition leads to the behavior may often depend on environmental conditions.
In summary, our data have provided consistent evidence for the association between the 40 bp VNTR polymorphism in the DAT1 gene and self-reported number of sexual partners using a sample of more than 2500 youth. Among the male young adults, possessing one or two alleles of the 10R is associated an 80–100% increase in the number of partners as compared with those possessing two alleles of the 9R. This finding is not evident among females. An equivalent interpretation can treat one or two 10Rs as the ‘wild type’, which amounts to about 91% of the individuals in the sample. Then the homozygotes for 9R can be considered as the ‘conservative’ or ‘undaring’ type whose reported number of sexual partners is about one half of the number reported by the wild type.
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This research uses data from Add Health, a program project designed by J Richard Udry, Peter S Bearman, and Kathleen Mullan Harris, and funded by a grant P01-HD31921 from the National Institute of Child Health and Human Development, with cooperative funding from 17 other agencies (www.cpc.unc.edu/addhealth/contract.html). Special acknowledgment is due to Andrew Smolen and John K Hewitt of the Institute for Behavior Genetics, University of Colorado for DNA isolation and genotyping. We express our appreciation for the comments made by anonymous reviewers. We gratefully acknowledge supports from NIH, P01-HD31921 to Add Health; R03 HD042490-02 and R03 HD053385-01 to Guang Guo; from NSF, SES -0210389 to Guang Guo.
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Guo, G., Tong, Y., Xie, CW. et al. Dopamine transporter, gender, and number of sexual partners among young adults. Eur J Hum Genet 15, 279–287 (2007). https://doi.org/10.1038/sj.ejhg.5201763
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