CBC linked to an article recently on the topic of race that I found interesting, partly because the author stated “racially pure” = “inbreeding”. Which is really true when you think about it – whites who marry whites and asians who marry asians are just inbreeding, but on a big enough scale where we aren’t worried about major birth defects.
However. There are many genetic diseases that are found primarily in one ethnic group or another – and I think this is a good example of inbreeding on a large scale. Northern Europeans and Ashkenazi Jews have the highest rates of carrying the gene for Cystic Fibrosis…Africans carry for Sickle-Cell Anemia….Asians carry for Thalessemia, etc.
Of course this had nothing to do with why I married Ang – I wasn’t shopping in the gene pool, naturally. But when we were expecting our first baby, I went to the OBGyn for the initial prenatal appointment for blood work. The midwife explained that I could have a blood screening for CF if I chose, but that it wasn’t mandatory. I remember her saying “you’re probably not a carrier, but I want you to know the test is available and it’s pretty simple.” I think a lot of women choose not to have these blood screenings, because by then you are already pregnant, so what’s the point? Unless you’re planning on aborting based on the results, it is seen by many women as unnecessary.
I don’t know what possessed me to have the test. I know I wouldn’t have aborted — I must have been struck by momentary curiosity.
When the results came back, the midwife was clearly surprised. She called me to let me know that I was indeed a carrier for CF. This meant that if my husband was white, the next step would be to test him. If both parents have the gene, you have a 1-in-4 chance with every pregnancy of having a child afflicted with the disease. (Among Europeans the rate of carrying for CF is something like 1 in 30 people.)
You cannot imagine how I sat there by the phone, struck by paralysis as I contemplated my child having CF. It is sheer terror to consider that future, of your baby’s life possibly being cut short. In an instant, I was amazed by my good fortune in marrying Ang.
I explained to the midwife that the father was Chinese. She seemed relieved. She said that his chance of carrying was so low, she didn’t think it imperative that we test him (I think the Asian rate of carrying this gene is 1/100).
There is no one in my family tree that suffered from CF – so until this point, none of us knew we were carriers. Which means that if we keep marrying white people, the odds that one of us ends up with a child with CF increase. So far we’ve been lucky! (And if I hadn’t had that test, we still wouldn’t know. I’m glad we found out about this before my brother had children, since he married a whitey.)
Marrying outside of our little inbreeding communities (ha) has a lot of good side effects, and I know firsthand how it feels to dodge a genetic bullet. There are diseases that can be passed from just one parent though, so I think it’s good to be aware of some of these things when you have kids – at least you’re prepared, so if one of your children exhibits some worrying symptoms, you have an idea of what to rule out. (I read recently that many Indian communities have high rates of Celiac disease, which is very common in Caucasians as well, so that’s a good one to be familiar with.)
Anyway, sometimes when I get pissy with Ang over something, I help myself get over it by remembering his positive attributes. Sometimes if I’m really angry, the only thing i can come up with is “Well at least his DNA spared our kids the possibility of a horrible disease.” So, you know, he’s got that going for him. Grrr.
***EDITED TO ADD: Ara on To Be or Not to Be wrote a great complementary piece to this featuring how inbreeding can also have the opposite effect (good things), resulting in mutations that help humans. She goes into a lot of info about how this has helped with HIV especially. A very interesting read!***

This is soooo off topic, but the Pennsylvania Amish community is providing a wealth of medical knowledge currently in tracing diseases like diabetes down to their exact gene. The amazing thing is that they are allowing the doctors to examine them, but the doctors who have moved in to study them have apparently been very diligent in respectfully gaining the Amish trust. All due to heavy (and I mean heavy) inbreeding. They don’t all have the same last name just because it sounds good….
On topic, that’s good to know about getting tested and carriers and stuff. You would think they’d suggest a test when you tell them you have begun TTC, or even just offer the tests during annuals. Seems a little odd to wait until a woman is pregnant to set her up for the scare of her lifetime.
By: Leah on June 18, 2008
at 1:03 pm
I agree with Leah, maybe they should just test for it during annual exams. If I don’t get into pharmacy school, I am really thinking of doing my masters in molecular biology/genetics.
As for genetics, your children lucked out CA. I learned from one of the pharmacists that Asians and Native Americans tend to lack a gene that breaks down alcohol. There are some medications, such as flagyl/metronidiazole, that you’re not supposed to have any alcohol mix with. That includes from over-the-counter medications, mouth washes, etc, otherwise, you’ll get extremely sick from the mix. The pharmacist actually counselled a patient and told them that she should avoid alcohol while taking and through 3 days after ending it, especially if she was of Native American or Asian descent or she’d become so violently ill, she’d wished she was dead. I thought he was exaggerating at first and asked him about it, and he was the one that told me about the missing gene that helps link the Native American population to the Asian. He also said that it is what makes Native Americans more prone to alcoholism since they can’t metabolize it like European/African descendants can. I was kind of surprised, but glad of my mixed heritage. Apparently I did not inherit that gene LOL.
There is also research being done on specifically Native American populations that are isolated because scientists have discovered that Native Americans and their descendants 2 to 1 have adult on-set diabetes versus other populations. They think if they could actually discover a gene defect compared to European populations, that they could one day have a cure for it. I think it looks quite promising.
Sorry, this is so long, but I love genetics..yeah I’m the stealth nerd muhahaha. Back to isolated populations. I do not know if you’re aware of this, but the cure for AIDS is actually close. Hmm.. actually I’ll just make a post of it over on my blog, so not to clutter it up over here…
By: ara0062 on June 21, 2008
at 10:00 pm
sorry I missed this – didn’t even know it got posted. lol (my drafts are in the cue and I was away from the puter for a bit)
Yes I totally know about the alcohol/Asian issue, since Ang had that problem. Gets drunk as a skunk on very little liquor. I don’t let him have vodka anymore – absolute no-go in this house. I could tell some horror stories but out of respect for my poor husband I will refrain.
Genetics always fascinates me too. Have you seen those tests you can pay to have done, where they analyze your DNA and tell you what ancestry you have? (Like what percentage european, asian, jewish, whatever)? I totally want to do that. Purely out of curiosity!
By: chineseambassador on June 23, 2008
at 2:33 am
Okay, well, CA, believe it or not, my degree allows me to do that LOL, but I don’t work for a company that does it LOL. We did it in my molecular lab, unfortunately, some of our supplies must have been old or contaminated, only 4 people out of both labs DNA came out. I was very disappointed, but for our first time, it was very interesting to do..for me
I SOOOO wanted mine to work, but it didn’t
One day though, one day
By: ara0062 on June 25, 2008
at 3:42 am
Oh, I am posting the article on AIDs over at my blog.. I referred to your article here..but I didn’t know how to tag it..linkback or whatever it’s called, so I just cited the web address
By: ara0062 on June 25, 2008
at 5:17 am
Thanks CBC for the reference. I just hope it might lend some hope to those who know folks with the horrible disease HIV/AIDS.
By: ara0062 on June 26, 2008
at 4:18 am