By Anthony Ellis, WCI Columnist

For better or for worse, the evolution of preventive care has progressed to the point of “direct-to-consumer” advertising and screening services that do not require a clinician’s orders. Since about age 40, my primary care doctor has ordered a set of “screening laboratory tests” every year with my routine physical. They are stored in the company's “app,” facilitating the comparison of previous results and spotting trends.

As time passed, insurance practices have changed. This annual preventive care has become harder to get without out-of-pocket expenses for copays and deductibles—or even the ubiquitous “prior authorization” or research as to “in-network” status. As I write this, my “PCP” is a nurse practitioner for the first time in my life. We moved to a new state, and she had the first opening when I called for my routine checkup appointment. The waiting times for routine appointments in our area can be 4-6 weeks for a PCP and up to six months for a specialist. To get an appointment for yearly labs and a checkup has, at times, been a bother, and it is now always an expense.

In 2024, I saw a Facebook advertisement for a direct-to-consumer service that offered access to a battery of blood tests, a U/A, an extended lipid panel, and other screening labs for a yearly fee. Of course, this “more than 100 biomarkers” was described as more comprehensive than most people usually get at their PCP. No doctor’s order or visit was required, and the fee was less than other bundles of labs I had seen. The fee for the service and their report interpretation was $499 yearly, and it is HSA-approved. I thought I would try it. There is no obligation to continue unless you see value.

Here’s what I learned.

 

Trying Something New

My current HDHP PPO suggests preferred providers to reduce copays and deductibles, but it still involves paying notable amounts for both. The “preferred providers” near us are mostly at the local city health clinic. My part-time employer is in Michigan, and the out-of-state coverage defaults to Aetna. Woe be to your wallet for any “out-of-network services.” I have also been billed for lab studies that were “not covered.” We are all healthy, and we have minimal care needs. In fact, none of us (except me) have sought treatment for symptoms in the two years since I dropped to half-time work. For many, getting yearly labs done involves a PCP appointment with a preferred provider and then paying plan deductibles. Even though most insurance covers a “wellness visit,” this may not include comprehensive labs, and it rarely includes a preventative care approach.

The usual “routine or preventive” labs that a PCP orders can vary widely, as can the approved insurance payments for these labs. In my current psychiatry position, we order a yearly CBC, Chem 20, Lipid profile, HbA1C, TFTs, Vitamin D level, and other labs individually based on medication regimens or comorbid conditions. These are the basic labs on the yearly profiles that my PCP has ordered in the past, along with a screening PSA test.

There are CEOs and VIPs who have yearly blood test screens that look for DNA markers for over 50 cancer types. If you want to add this Galleri cancer screening, you can for an additional $899. If you want other add-on labs, you can pay for them based on your individual or family history. For example, I paid for a genetic assay of my ApoE allele status due to a notable family history of Alzheimer’s disease (an extra $129). This type of “preventative screening” is becoming more commonly available. There are longevity centers and concierge clinics that offer many types of assessments with testing that include labs, a physical exam, a nutritional evaluation, a cognitive screening test, whole body imaging exams, cardiac stress tests, and coronary artery calcium scoring. I read about one recently that a wellness journalist chose, and the appointment and tests were all done in five hours at one visit.

The service I chose for $499 (plus the extra bit for my ApoE allele status) used a national laboratory service (Quest Diagnostics), and the appointment was set in the app for the service with two appointments a week apart. The lab was within a half hour of my house, and I was familiar with the lab company. I was given detailed instructions to follow in the days before the blood draw for stopping supplements, fasting for eight hours, and hydrating adequately.

I am not saying that these services replace routine follow-up care or chronic disease management. I have no new symptoms and very few chronic medical issues. I tend to get all the recommended screening labs or studies to maximize my chances of living a long, healthy life. I eat a healthy diet. I had a coronary artery calcium scan that was ordered by my PCP in 2020 when I was 56. Like many retirees looking to live long enough to spend some of their savings, we hike to stay fit. I swim two or three days a week and do body weight strength training two days a week. My weight is within 10% of my weight at age 35, and I do not smoke.

Fortunately, I do not have HTN, DM, or a known familial lipid disorder. I am simply trying to prevent or detect what I can on the list of health issues that can ruin my quality of life or kill a fortunate, healthy retiree like me.

More information here:

Don’t Push Your Luck (Physically or Financially)

Functional Longevity: What Use Is Retirement If You Can’t Move and Think?

 

Was It Worth It?

Is an ounce of prevention worth a pound of cure? Are any of these services effective in preventing or reducing illness sequelae, detecting cancer, or finding coronary issues before the widow maker MI, like one of my coworkers had? Are these services “worth it” for a healthy person, or are they better for someone with more health issues? Do they provide actionable data? If not, why are CEOs lining up for them? Do they cause more harm than good with “false positives” that require follow-up testing? Do they provide any peace of mind? Does one really need LDL fractionation, or is this mostly a way to get your hard-earned dollars?

These are good questions with few data-driven answers.

In my case, I avoided one or two PCP appointments where I would try to convince the clinician to do more extensive testing than the norm. Going to the doctor takes time, and I always have copays. The labs are not always covered. It can easily add up to $500 unless I pick the “in-network provider,” obtain “covered lab services,” and take multiple trips and hours of time. There may be little discussion of labs beyond “they were generally normal.” Some clinicians do not always cover nutrition or discuss useful supplements. In fact, based on the resident forums I read, it seems the “rich patients eating Chia seeds, drinking green smoothies, and taking a handful of supplements” are routinely mocked.

Asking for specific assessments can step on the clinician’s toes a bit and brings up the adage: “The doctor who has him or herself as a doctor has a fool for a doctor.” I have never been offered all these labs at once. I was never told to get an ApoE phenotype test despite my family history. I have also had clinicians find it humorous or off-putting when I tell them I love my life and simply do not want to die prematurely and leave my family, retirement savings, and maximum Social Security benefits on the table.

The “biomarker” results were available in about two weeks, and they came with a detailed, fairly cookie-cutter discussion of recommendations and actions to take based on the out-of-range values. Prior to the tests, I predicted my ApoE allele status as E3/E4 based on allele prevalence and family history. Mine turned out to be E2/E3. This is in the lower risk quartile where the rare E2/E2 phenotype sits. In fact, E2/E3 is the next best at ~11% of the population. The worst phenotype is E4/E4, and it's present in about 2% of the population.

The six possible APOE genotypes are: E2/E2 (1%), E2/E3 (11%) (this was my result), E2/E4 (2%), E3/E3 (61%), E3/E4 (23%), and E4/E4 (2%) (the worst).
ApoE4 increases Alzheimer’s risk. Having at least one ApoE4 gene doubles or triples the risk of developing Alzheimer's disease. A rare group has two ApoE4 alleles. Having two copies of ApoE4 increases the risk of getting Alzheimer's disease even more—about eight- to twelve-fold.

In one meta-analysis of pre-clinical amyloid deposition, the ApoE phenotype was correlated with age of accumulation: “The age at which 15% of the participants with normal cognition were amyloid positive was approximately 40 years for APOE ε4ε4 carriers, 50 years for ε2ε4 carriers, 55 years for ε3ε4 carriers, 65 years for ε3ε3 carriers, and 95 years for ε2ε3 carriers.”

My standard lipid profile results (Total Cholesterol, HDL, LDL, and Triglycerides) were about the same as always. This service included an LDL fractionation to look at particle size, ApoB, and LP(a). The new data here was that my “LDL small particle” number was high, and other LDL fractionation levels were abnormal. I had 90/106 markers “in range.” My Hb and Hct were slightly elevated, a consequence of currently living at 2,900 feet elevation. I had normal HDL, Lipoprotein (a), High Sensitivity CRP, and Triglycerides, and I do not have a family history of CAD or early MI. One new finding was that I have notable levels of anti-thyroid antibodies. This had never been checked before.

More information here:

Health Insurance in Early Retirement

How to Save On Healthcare Costs

 

My Response to the Lab Results

Overall, the added peace of mind from the ApoE allele and the overall assessment were worth the money spent. I think I may have spent a similar amount on copays and deductibles had I gone the usual PCP route.

What did this change for me? Well, I now know to monitor T4 and TSH across time for signs of clinical Hashimoto’s. I know that my Alzheimer’s risk is low with my phenotype (E2/E3), especially given my lifestyle, diet, and exercise levels. I know that, despite healthy HDL and normal LDL and Triglycerides, I may have unquantifiable cardiovascular risk from LDL small particles, elevated ApoB, and elevated homocysteine levels. I looked back on old labs, and I noticed an elevated homocysteine level from five years ago. But I received no recommendations from my PCP on this. I read that lowering this by 20% (with B Vitamins) has not proven to correspond to any lower cardiac or stroke risk, another “fascinoma” like LDL fractionation. It is not entirely clear that “managing” these will do anything spectacular.

Still, I decided to further reduce my red meat intake, increase my intake of non-peanut nuts, and eat even more vegetables. I also decided to try the “top supplements” suggested by the service based on my results. I looked them up and read about each of them. A two-month supply of all of them was about $125. One can look up each supplement and read any available research on its effectiveness. In my experience, it is rare to get specific recommendations based on your “biomarkers” and then have follow-up labs to determine if target values change. My labs will be checked again in six months. At the least, it is interesting, even if it is a bit neurotic. For the next six months, I am one of those “rich people who want to live forever,” but at least it is not “by supplements alone.”

Of course, I will keep swimming, hiking, doing body weight exercises, reading, solving the New York Times daily word puzzles, and writing for an audience. My wife and I also signed up for a “vacation half marathon” in the Great Smoky Mountains in September 2025. We will continue to hike all our local favorite trails that were not damaged or closed by Hurricane Helene’s rampage. We took vacations to hike Sedona, Arizona, and we hiked 80 kilometers of the Amalfi Coast of Italy in 2024. Hiking trips are more fun than vitamins and supplements.

Good luck to me and my LDL fractionation and homocysteine levels. I will still see a PCP yearly, but I am still looking for one like my prior PCP in Michigan. She was excellent, and I miss her.

Would you or have you ever tried a service that offers expanded labs? What conclusions did you reach? Did anything in your life change?