When Screening for Genetic Abnormalities, Noninvasive Prenatal Tests Often Result in False Positives—Here's What That Means
Earlier this week, The New York Times published a groundbreaking analysis of noninvasive prenatal tests (NIPTs), finding that they produce inaccurate results up to 85 percent of the time. If you are a pregnant person, or someone who hopes to become pregnant in the future, this news may have caught you off guard and made you feel concerned.
That's totally understandable—these are worrisome stats and you may be unsure about what this all means for you. You may be wondering if you should get any NIPT screenings at all. If you've received concerning results from one of these tests, you may feel unsure of what the results mean and what additional steps you should take.
The topic of NIPTs can be a confusing one, and the information can feel very technical and difficult to understand. Let's break it all down and look at what NIPTs actually are, what they're used for, and how this new data from The Times fits into it all.
What Are NIPT Tests?
NIPT tests are screening tests used to find out if your baby might be born with a genetic abnormality. These tests are noninvasive and analyze a sample of your blood for DNA from your fetus. During pregnancy, small fragments of your baby's placenta DNA end up in your bloodstream and can be detected and analyzed. These free-floating DNA fragments are called cfDNA and may contain information about your baby's genetic makeup.
Some folks use NIPT tests to try to find out their baby's sex under the assumption they are learning their baby's gender. Unfortunately, these tests don't accurately determine one's gender identity and they can also result in unnecessary worries.
It's important to understand that NIPT tests are screening tests. In other words, they are not definitive results about what genetic abnormalities your baby might have. They can tell you whether your baby has an increased or decreased risk of having a genetic abnormality, not whether they actually do.
You will need a diagnostic test, such as amniocentesis and chorionic villus sampling to confirm or deny the results from a NIPT test. These diagnostic tests can be informative, but they slightly increase your risk of miscarriage.
How Common Are False Positives?
NIPT tests can screen you for many different genetic abnormalities. According to The New York Times, they are thought to be highly accurate in terms of accessing your baby's risk for Down syndrome, which was one of the first uses of these tests. However, when it comes to more rare genetic abnormalities, there are more possibilities for false positives.
In their independent investigation, The New York Times looked at studies and interviewed researchers about five different prenatal tests that screened for rare genetic conditions. The screenings they analyzed included tests that looked for DiGeorge syndrome, 1p36 deletion, Cri-du-chat syndrome, Wolf-Hirschhorn syndrome, and Prader-Willi and Angelman syndromes.
These are extremely rare conditions—for example, Wolf-Hirschhorn syndrome affects 1 in 20,000 births—but can cause lifelong physical and intellectual disabilities. Results varied from one test to another, but The Times found that these tests consistently gave inaccurate results on average 85 percent of the time.
What Does This Mean For You?
Hearing that your baby might have a genetic condition that could result in disability (and in some cases death) can be difficult information to absorb. Learning that these tests can be highly inaccurate a lot of time may make you question whether they are even worth pursuing.
These are valid concerns, and it's part of why The Times made this information public for parents. The truth is, though, the decision to get one of these tests is an individual choice, one you should make after a conversation with your medical team, rather than based on a knee-jerk reaction to some unsettling statistics.
Should You Get A NIPT Test?
For many expectant parents, getting screened for a rare genetic condition that comes with a high probability of inaccurate results, is simply not worth the stress. Blood tests for genetic abnormalities are usually conducted in the first 10-14 weeks of pregnancy, and follow-up diagnostic tests are usually done between the 15th and 20th week of pregnancy.
So, if your NIPT test tells you that your baby might have one of these conditions, there will be a waiting period until you are able to get a diagnostic test to tell you whether your baby does, in fact, have one of these conditions. Then you have to wait for results for the diagnostic tests.
All of the waiting and the anxiety that comes with testing may not be worth it for you, especially when considering a screening test with a high rate of false positives. However, people who have known risk factors, such as genetic conditions that run in their family may decide that these tests are vital.
The American College of Obstetricians and Gynecologists (ACOG) recommends that all pregnant individuals be offered NIPT screenings whether or not they have a known risk factor, including advanced age. This doesn't mean that your doctor will recommend that you get screened for every genetic condition, though.
For example, almost all health care providers recommend that parents over the age of 35 be screened for Down syndrome but may not recommend one of the more rare genetic screenings that The Times investigated. The decision about which genetic conditions to screen for should be done in collaboration with your health care provider.
Where To Go From Here
Seeing a scary headline about genetic tests and high false positives can be enough to increase your blood pressure; but knowledge is power.
Even though you may feel overwhelmed as you absorb this information, keep in mind that you have choices when it comes to your prenatal care. Learning that screenings tests like NIPTs sometimes can be inaccurate is a great opportunity for you to have an open discussion with your health care provider about what your options are and which screening tests make sense for you and your pregnancy.
If you are personally dealing with some upsetting results from a NIPT screening and waiting for further confirmation, know that you aren't alone: Many parents have navigated these extremely stressful situations.
Again, speaking to your health care provider about what this means, how accurate these results are, and what your next steps should be, is important. If you feel that your provider isn't listening to you, or isn't communicating in a clear way, you might consider switching providers or getting a second opinion.
Importantly, the mental health impact of dealing with screening, testing, and upsetting results should not be underestimated. If you are experiencing heightened stress or anxiety, please reach out to your health care provider or a mental health professional. You deserve to feel balanced and well.
I know many women who was screened with a FALSE POSITIVE. Their baby came out as mini scholars with NO issues at all. Imagine them aborting someone so special because of a discrepancy. I know women who had FALSE NEGATIVE and their baby came out with Down syndrome.
This test needs to be further investigated and people should definitely sue.
My friend first test came out negative once she put mixed race, then for the second test she put a different race and it came back positive. Her baby came out absolutely fine!
I wouldn’t recommend this test to anyone unless you really urge to get it because of family history. But I’d advise not to.
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This is by far one of the worst, most misleading, and most fear-mongering article I’ve read in a long time. Even the subtitle is wrong and completely missing the point of the New York Times investigation. Yes, for rare conditions the positive predictive value (PPV) on these types of tests can be low. But that is NOT the same as falsely claiming that 85% of NIPTs come back as false positives!!!! Obviously the vast majority of these tests come back NORMAL. She is trying to convey that out of the positive results for the microdeletions (but notably NOT for common trisomies which is stated misleadingly at best and at worst purposefully manipulative) the PPV is low. Please do not listen to non medical writers who pretend to understand things well beyond their scope. Genetic counselors (not even MENTIONED IN THE ARTICLE) are trained professionals who are specifically suited to counseling patients preferably PRIOR to having this test so that they can understand what the test can and cannot do. There are so many errors and false information in this article I don’t even know where to start. This should be taken down immediately before pregnant people begin to reject very accurate screening for genetic conditions due to false statements in this piece. Ignore this altogether and make an appointment with a genetic counselor PLEASE!!!!Read More