Saletan's claim that a recent study's data can be used to show a genetically based cognitive disadvantage for Africans is wrong
[Saletan was quickly taken to task, with bloggers leading the charge, for his supporting evidence and methodology in the series as a whole, as I summarize in another post. But the IQ-breastfeeding claim has, it seems, so far escaped notice. ]
The study itself, published in the highly respected journal PNAS, suggests a link between breastfeeding, individual genetic makeup, and cognitive development. That breastfed babies, all else being equal, tend to end up with higher IQs than those who are not breastfed is a well-established fact. This study links that IQ boost from breastfeeding to a specific gene. The gene in question, called FADS2, codes for a key element the of body’s machinery for processing fatty acids, and breast milk is high in certain fatty acids thought to be important in brain development.
The researchers examined two large sample groups (one from New Zealand and one from Britain), and found that breastfed babies ended up with higher IQs than non-breastfed babies only if they had a certain form of the gene, as did the large majority of the sample. In the small minority of babies who lacked this form of the gene, no IQ benefit from breastfeeding was seen. Among all breastfed babies, those with the IQ-boosting version of FADS2 had a four-point IQ advantage over those who lacked it — a meaningful and provocative result suggesting a very specific interaction between nature (the children's genetic makeup) and nurture (whether or not they were breastfed).
Saletan uses the study's results combined with gene frequencies available in a research database to claim that this IQ-boosting gene is less prevalent in people of African descent by a factor of two to four as compared to other population groups around the world, and by extension that Africans are "cognitively disadvantaged." In fact, this conclusion is completely unsupported by any data and is the result of unsound methodology. (Continue reading...)
The study
The researchers tested for different forms of the fatty-acid processing gene in their sample groups. These different forms were the product of differences of just one letter in the DNA code -- a "C" rather than a "G", for instance. Such places of variation are known as SNPs (single nucleotide polymorphisms, pronounced "snips"). SNPs are specific spots where the gene sequence is known to vary by one letter in the population. SNPs are relatively rare in the DNA code (because the vast majority of our DNA is identical with that of everyone else on the planet), and once identified (or "mapped") provide a convenient way to map genetic differences.
Any single gene can have many SNPs scattered throughout it. To select SNPs to examine in the study, the study's authors made use of the International HapMap Project, which has created a database and map of SNPs in the human genome. The SNP map and data are based on DNA sequences from four small samples of populations around the world: Yoruba from Ibadan, Nigeria; Utah residents of northern and western European ancestry; Japanese from Tokyo, and Han Chinese from Beijing. In HapMap's database, there are over 40 SNPs identified in the sequence of the FADS2 fatty-acid processing gene. Making educated guesses about which SNPs were important to the gene's function, the study's authors chose two of these SNPs to test in their Britain and New Zealand sample groups.
The result for the first SNP (called "rs174575") were very meaningful. At this SNP, there are two variants in the human population: C and G. The C-form is the form that seems to enable an IQ boost in breastfed children. In both study populations, breastfed babies with at least one copy of the C-form scored several IQ points higher later in life than non-breastfed babies with at least one C-copy. (Remember that we all have two copies of every gene.) Those that did not have a single C-copy (what we can call the G/G group) saw no IQ benefit associated with breastfeeding. The G-version was also the least common: the G/G group made up just 10% of the British study group and 7% of the New Zealand study group.
The results from the second SNP ("rs1535") were not so conclusive. Like the first SNP, the G-version is least common and showed no propensity to boost IQ scores in the presence of breast milk. The more common version (in this case, the A version) did boost IQ scores in breastfed children, but only in the British sample group. In the New Zealand results the data showed no link between the variations of the FADS2 gene at this SNP and IQ scores in breastfed children.
The study provided strong evidence that breastfeeding boosts IQ only if you have a particular version of the fatty-acid processing gene. Specifically, the C-version of the first SNP (rs174575) provides the IQ boost, while the G-version does not. The HapMap database provides the frequencies of the two different versions for each of its populations. So Saletan looked up what percentage of each HapMap population is G/G.
| Utah, U.S.A. (European heritage) | 5% |
| Beijing, China (Han) | 2% |
| Tokyo, Japan | 2% |
| Ibadan, Nigeria (Yoruba) | 10% |
Saletan takes this to be an salient difference in racial IQ capability:
"The Africans are twice as likely as the Americans, and four times as likely as the Asians, to start life with a four-point IQ deficit out of sheer genetic misfortune. Don't tell me those Nigerian babies aren't cognitively disadvantaged. Don't tell me it isn't genetic. Don't tell me it's God's will. And in the age of genetic modification, don't tell me we can't do anything about it....No, we are not all created equal."
In fact the data shows nothing of the sort. Nigerian babies aren't cognitively disadvantaged. Saletan's reasoning is wrong on at least three distinct counts, any of which alone is enough to debunk any claim about racial IQ differences that can be made based on this study's data or any extension of it. (To be clear, Saletan's reasoning is not represented in any way in the actual study, which is not about race).
First, the frequency of the G/G genotype in the Yoruba cannot be taken as representative for Africa as a whole (and by extension, for people of African descent around the world). The size of the HapMap samples from which the map was made is small: each was less than 60 unrelated people. HapMap is representative in the sense that it contains most single-site human genetic variations in the world (it was constructed from four pretty spread-out groups in order to achieve this), but this doesn’t mean that the gene frequencies in these small populations are representative of large, continental populations for any given variation. HapMap's own guidelines for using their data make this clear: "These samples should not be described merely as 'African,' 'Sub-Saharan African,' 'West African,' or 'Nigerian,' since each of those designators encompasses many populations with many different ancestral geographies", with similar statements for the other populations sampled.
Furthermore, the percentage of study subjects who were G/G -- all of them whites from Britain and New Zealand -- is as high as in the Yoruba sample.
| British sample group | 7% |
| New Zealand sample group | 10% |
(Note: these numbers are not directly presented in the study but are easily calculated.)
As you can see, the percentage of the New Zealand study group who are G/G is just as high as the HapMap Yoruba. These numbers illustrate the mistake of extending the HapMap frequencies to larger populations, as well as showing that even if we were to take the Yoruba sample to be representative for some larger group (a dubious proposition, for reasons stated above), white populations do not, in reality, have a more "favorable" genetic distribution in this case. (Both the New Zealand and the British sample groups in the study excluded nonwhites, as stated in the Methods section of the paper, and both sample groups contained over 1,000 people).
Second, the results found for the other SNP (rs1535) shouldn't be ignored. If you look at the British group only, the results are almost identical to those for the first SNP: people with only the less common variety (coincidentally also the "G" version) showed no IQ boost from breastfeeding, while those with at least one copy of the other version (A in this case) got the IQ boost. But this result wasn't replicated in the New Zealand group, where there was no association between the SNP variants and IQ. (Here's the study's raw data, reproduced). Nevertheless, as the British result for rs1535 was just as solid as the rs174575 results, it certainly would be fair to say that such a link is possible. Here's are HapMap gene frequencies for the "bad" G/G version of rs1535:
rs1535: Percentage of study participants who are G/G
| Utah, U.S.A. (European heritage) | 13% |
| Beijing, China (Han) | 16% |
| Tokyo, Japan | 11% |
| Ibadan, Nigeria (Yoruba) | 2% |
The proportions are decisively reversed in "favor" of the Yoruba.
Third, both the British and New Zealand sample cohorts excluded nonwhite participants. If you wish to show that genetic differences across different races lead to different IQ potentials, you need actual data on each of the groups you are trying to make claims about. In other words, since the study was conducted entirely on white sample groups, the results of this study can't be used to make claims about differences between white and nonwhite populations.
In his article, Saletan presents his conclusions as if they are as solid as the legitimate study he is piggybacking on, when in fact they are of a different kind altogether. Rather, his conclusions are the mixed-up result of some hasty research in an unfamiliar field, seemingly in pursuit of evidence to support his broader thesis.
Resources
- The study (only the abstract is free): Moderation of breastfeeding effects on the IQ by genetic variation in fatty acid metabolism (Caspi et al, PNAS 2007)
- Study data (group IQ scores and genotype frequencies).
- To view the HapMap Project map for FADS2, go here and type "FADS2" into the search box. Or use this direct link.
- HapMap population frequencies for rs174575 and rs1535