Response by SuperOme
Proteomic Response Report · Clinician edition
How this patient's biology responded to 12 weeks of semaglutide.
About 1,000 plasma proteins measured at four timepoints on one plate, read against the patient's own baseline noise, and anchored to accredited clinical chemistry.
- Participant
- M.K. · R-0417 · 52 F
- Program
- GLP-1 initiation (semaglutide)
- Indication
- Weight management, prediabetes (HbA1c 6.1%)
- Ordering clinician
- Dr. A. RiveraMeridian Longevity Clinic, Austin TX
- Timepoints
- Baseline · Week 4 · Week 8 · Week 12
- Collection
- Home capillary dried blood, 4 samples returned together
- Platform
- Multiplex proteomics panel v2.1 (pg/mL)
- Report date
- 12 Jun 2026
Research Use Only. Proteomic results are not a diagnosis; accredited clinical chemistry values are the only results on which clinical action should be taken.
Response by SuperOmeAt a glance
M.K. · R-0417 · GLP-1 initiation (semaglutide)
Three things to know before the next visit.
Improved
Metabolic, inflammatory, hepatic and endothelial markers moved together and agree with the clinic HbA1c, ALT, lipids and hs-CRP.
Unchanged
No kidney or neuro marker left the patient's own noise band. Reported as a result, not an omission.
Review with the patient
A muscle/bone pattern consistent with lean-mass loss, and a gut-epithelial marker that rose during the nausea weeks. Neither is diagnostic.
Proteins in this report
68
in curated organ panels.
Status split
- 21
- improved
- 41
- unchanged
- 5
- review
- 1
- below quantification
Next window
Week 16–18, after 4+ weeks at a stable dose. Re-check muscle/bone and gut panels; consider DXA before the next dose step.
Reading rule. Teal = moved in the direction the program intends. Stone = did not move beyond this patient’s own noise. Amber = moved in a direction worth a conversation. A protein is never flagged on a population reference range alone; the comparison is always to the patient’s own baseline.
Response by SuperOmeClinical anchors
M.K. · R-0417
Accredited laboratory values and program context.
Venous draws in clinic at Baseline and Week 12, run by a CLIA-accredited laboratory. These are the values on which clinical decisions should rest. The proteomic panels that follow are read against them.
Weight
Improved91.4 → 83.7 kg · −8%
BMI
Improved33.1 → 30.3 kg/m² · −8%
HbA1c
Improved6.1 → 5.6 % · −8% · reference < 5.7
Fasting glucose
Improved108 → 94.0 mg/dL · −13% · reference 70–99
Fasting insulin
Improved17.8 → 10.2 µIU/mL · −43% · reference 2.6–24.9
ALT
Improved38.0 → 27.0 U/L · −29% · reference 7–35
AST
Improved31.0 → 26.0 U/L · −16% · reference 8–33
Lipase
Review31.0 → 36.0 U/L · +16% · reference 13–60
Creatinine
Unchanged0.82 → 0.84 mg/dL · +2% · reference 0.57–1.00
eGFR (CKD-EPI 2021)
Unchanged88.0 → 86.0 mL/min/1.73m² · −2% · reference > 60
LDL-C
Improved131 → 112 mg/dL · −15% · reference < 100
ApoB
Improved104 → 89.0 mg/dL · −14% · reference < 90
Triglycerides
Improved168 → 121 mg/dL · −28% · reference < 150
hs-CRP
Improved3.6 → 1.8 mg/L · −50% · reference < 1.0 low risk
hs-cTnI
Unchanged< 3 → < 3 ng/L · reference < 16
NT-proBNP
Unchanged42.0 → 38.0 pg/mL · −10% · reference < 125
Grip strength (dominant)
Review26.0 → 24.0 kg · −8% · reference ≥ 20 (F)
Weight
Dose schedule
- 0.25 mg from week 0 to week 4
- 0.5 mg from week 4 to week 8
- 1.0 mg from week 8 to week 12
Weekly subcutaneous. Adherence 12/12 injections logged.
Reported effects
| Wk 1–2 | Mild nausea after injection day | mild |
|---|---|---|
| Wk 3–6 | Nausea most days; two episodes of vomiting (wk 5, dose step) | notable |
| Wk 7–9 | Constipation; resolved with fibre + fluids | mild |
| Wk 10–12 | No GI symptoms reported; early satiety only | resolved |
Lipase rose within the reference interval (31 → 36 U/L). No abdominal pain reported. Noted because pancreatitis is the threshold alarm on this drug class; no action implied.
hs-cTnI and NT-proBNP are reported from the accredited lab, not from the proteomic panel. Affinity proteomics does not deliver clinical-grade troponin quantification.
Response by SuperOmeMetabolic & GLP-1 axis
M.K. · R-0417 · GLP-1 initiation (semaglutide)
Metabolic & GLP-1 axis
Insulin demand fell, adipokines moved toward a leaner profile, and appetite hormones shifted in the direction expected on a GLP-1. This is the clearest response in the report and is concordant with the clinic HbA1c and fasting glucose.
System verdict
Improved
Organ response index +2.8× noise band · 12 proteins · 10 moved / 2 unchanged / 0 review
INS InsulinFasting insulin; concordant with clinic value
Improved640 → 370 pg/mL · −42% · 3.0× noise
C-peptide Connecting peptide (C-peptide)
Improved2.9 → 1.9 ng/mL · −34% · 2.9× noise
Pro-insulin Pro-insulinPro-insulin:insulin ratio also fell
Improved210 → 125 pg/mL · −40% · 2.7× noise
LEP LeptinTracks fat-mass loss
Improved28.4 → 17.1 ng/mL · −40% · 3.6× noise
ADIPOQ Adiponectin
Improved6.1 → 7.9 µg/mL · +30% · 3.3× noise
FGF21 Fibroblast growth factor 21
Improved312 → 188 pg/mL · −40% · 2.2× noise
FABP4 Fatty acid-binding protein, adipocyteAdipocyte-derived
Improved27.8 → 19.2 ng/mL · −31% · 2.6× noise
IGFBP1 Insulin-like growth factor-binding protein 1Rises as insulin falls
Improved12.1 → 23.6 ng/mL · +95% · 5.9× noise
IGFBP2 Insulin-like growth factor-binding protein 2
Improved181 → 262 ng/mL · +45% · 3.4× noise
RBP4 Retinol-binding protein 4
Unchanged31.6 → 27.4 µg/mL · −13% · 1.3× noise
GHRL Appetite-regulating hormoneRises with weight loss; expected
Improved618 → 790 pg/mL · +28% · 1.9× noise
PYY Peptide YY
Unchanged96.0 → 114 pg/mL · +19% · 1.1× noise
Trajectory shows Baseline → Week 4 → Week 8 → Week 12. “Vs noise” is the Week 12 change divided by this patient’s expected within-person variation for that protein. Changes under 1.5× are reported as unchanged. The noise is the technical replicates on the same plate plus cohort within-person variance. Concentrations are calibrant-relative values from dried capillary blood and are not interchangeable with venous clinical assays of the same analyte.
Response by SuperOmeInflammation
M.K. · R-0417 · GLP-1 initiation (semaglutide)
Inflammation
Acute-phase and adipose-linked inflammation fell. TNF, CCL2 and GDF15 did not move beyond this participant's own noise band; GDF15 is worth re-checking at the next window because it rises on several metabolic drugs.
System verdict
Improved
Organ response index +1.1× noise band · 10 proteins · 5 moved / 5 unchanged / 0 review
CRP C-reactive proteinConcordant with clinic hs-CRP
Improved3.8 → 1.9 mg/L · −50% · 2.5× noise
SAA1 Serum amyloid A-1 protein
Improved6.2 → 3.1 µg/mL · −50% · 2.3× noise
IL6 Interleukin-6
Improved3.1 → 2.0 pg/mL · −35% · 1.9× noise
IL1RN Interleukin-1 receptor antagonist proteinIL-1 receptor antagonist
Improved420 → 290 pg/mL · −31% · 2.2× noise
S100A9 Protein S100-A9Calprotectin subunit
Improved1,120 → 790 ng/mL · −29% · 1.8× noise
TNF Tumor necrosis factor alpha
Unchanged1.9 → 1.8 pg/mL · −5% · 0.4× noise
CCL2 C-C motif chemokine 2
Unchanged240 → 226 pg/mL · −6% · 0.4× noise
IL18 Interleukin-18
Unchanged241 → 232 pg/mL · −4% · 0.3× noise
CXCL8 Interleukin-8
Unchanged6.0 → 5.7 pg/mL · −5% · 0.3× noise
GDF15 Growth/differentiation factor 15Monitor; drug-associated rise is common
Unchanged890 → 985 pg/mL · +11% · 1.1× noise
Trajectory shows Baseline → Week 4 → Week 8 → Week 12. “Vs noise” is the Week 12 change divided by this patient’s expected within-person variation for that protein. Changes under 1.5× are reported as unchanged. The noise is the technical replicates on the same plate plus cohort within-person variance. Concentrations are calibrant-relative values from dried capillary blood and are not interchangeable with venous clinical assays of the same analyte.
Response by SuperOmeLiver
M.K. · R-0417 · GLP-1 initiation (semaglutide)
Liver
Hepatocyte-derived markers moved toward lower liver fat and lower transaminase release, in step with the accredited ALT/AST. Fibrosis-associated markers did not change, which is the expected result over 12 weeks.
System verdict
Improved
Organ response index +1.2× noise band · 8 proteins · 4 moved / 4 unchanged / 0 review
GPT Alanine aminotransferase 1ALT protein; clinic ALT 38 → 27 U/L
Improved1.9 → 1.3 ng/mL · −32% · 2.4× noise
GOT1 Aspartate aminotransferase, cytoplasmicAST protein
Improved2.4 → 1.9 ng/mL · −21% · 1.7× noise
FABP1 Fatty acid-binding protein, liverLiver fatty-acid binding protein
Improved18.2 → 11.9 ng/mL · −35% · 2.3× noise
FGF19 Fibroblast growth factor 19
Improved112 → 151 pg/mL · +35% · 1.7× noise
HGF Hepatocyte growth factor
Unchanged620 → 540 pg/mL · −13% · 0.9× noise
TIMP1 Metalloproteinase inhibitor 1Fibrosis-associated
Unchanged151 → 143 ng/mL · −5% · 0.6× noise
SERPINA1 Alpha-1-antitrypsin
Unchanged1.42 → 1.39 mg/mL · −2% · 0.3× noise
AFP Alpha-fetoprotein
Unchanged2.1 → 2.2 ng/mL · +5% · 0.5× noise
Trajectory shows Baseline → Week 4 → Week 8 → Week 12. “Vs noise” is the Week 12 change divided by this patient’s expected within-person variation for that protein. Changes under 1.5× are reported as unchanged. The noise is the technical replicates on the same plate plus cohort within-person variance. Concentrations are calibrant-relative values from dried capillary blood and are not interchangeable with venous clinical assays of the same analyte.
Response by SuperOmeCardiovascular & endothelium
M.K. · R-0417 · GLP-1 initiation (semaglutide)
Cardiovascular & endothelium
Endothelial activation markers fell; PCSK9 and natriuretic peptide drifted down but stayed inside the noise band. Cardiac troponin T is below quantification at every timepoint, which is normal in a healthy heart; it is not a negative result and is not a substitute for a clinical hs-cTnI.
System verdict
Improved
Organ response index +1.2× noise band · 9 proteins · 2 moved / 6 unchanged / 0 review / 1 below LLOQ
SELE E-selectinE-selectin
Improved42.0 → 31.0 ng/mL · −26% · 2.2× noise
VCAM1 Vascular cell adhesion protein 1
Unchanged612 → 538 ng/mL · −12% · 1.3× noise
ICAM1 Intercellular adhesion molecule 1
Improved241 → 206 ng/mL · −15% · 1.6× noise
MPO Myeloperoxidase
Unchanged61.0 → 48.0 ng/mL · −21% · 1.3× noise
PCSK9 Proprotein convertase subtilisin/kexin type 9Clinic LDL 131 → 112 mg/dL
Unchanged281 → 249 ng/mL · −11% · 1.1× noise
APOA1 Apolipoprotein A-I
Unchanged1.31 → 1.36 mg/mL · +4% · 0.6× noise
ANGPT2 Angiopoietin-2
Unchanged2.1 → 1.9 ng/mL · −10% · 0.7× noise
NPPB Natriuretic peptides BTotal BNP-gene product, not NT-proBNP
Unchanged28.0 → 25.0 pg/mL · −11% · 0.7× noise
TNNT2 Troponin T, cardiac muscleBelow LLOQ at all four timepoints
Below LLOQ< 5 → < 5 pg/mL
Trajectory shows Baseline → Week 4 → Week 8 → Week 12. “Vs noise” is the Week 12 change divided by this patient’s expected within-person variation for that protein. Changes under 1.5× are reported as unchanged. The noise is the technical replicates on the same plate plus cohort within-person variance. Concentrations are calibrant-relative values from dried capillary blood and are not interchangeable with venous clinical assays of the same analyte.
Response by SuperOmeKidney
M.K. · R-0417 · GLP-1 initiation (semaglutide)
Kidney
No kidney marker moved outside this participant's own noise band. On a GLP-1 with rapid weight loss, an unchanged kidney panel is the result you want to see; it is reported here as explicitly unchanged rather than omitted.
System verdict
Unchanged
Organ response index 0.0× noise band · 6 proteins · 0 moved / 6 unchanged / 0 review
CST3 Cystatin-CCalibrant-relative; not IFCC-traceable
Unchanged0.86 → 0.88 mg/L · +2% · 0.3× noise
HAVCR1 Hepatitis A virus cellular receptor 1KIM-1, tubular injury
Unchanged95.0 → 102 pg/mL · +7% · 0.5× noise
CLU Clusterin
Unchanged118 → 121 µg/mL · +3% · 0.3× noise
SPP1 OsteopontinOsteopontin
Unchanged38.0 → 34.0 ng/mL · −11% · 0.8× noise
TIMP2 Metalloproteinase inhibitor 2
Unchanged84.0 → 86.0 ng/mL · +2% · 0.3× noise
EGF Pro-epidermal growth factor
Unchanged410 → 430 pg/mL · +5% · 0.4× noise
Trajectory shows Baseline → Week 4 → Week 8 → Week 12. “Vs noise” is the Week 12 change divided by this patient’s expected within-person variation for that protein. Changes under 1.5× are reported as unchanged. The noise is the technical replicates on the same plate plus cohort within-person variance. Concentrations are calibrant-relative values from dried capillary blood and are not interchangeable with venous clinical assays of the same analyte.
Response by SuperOmeMuscle & bone
M.K. · R-0417 · GLP-1 initiation (semaglutide)
Muscle & bone
This is the panel to discuss. IGF-1 fell, follistatin-like 3 rose and two bone-turnover markers rose, a pattern consistent with reduced lean mass or reduced mechanical loading during rapid weight loss. The clinic grip-strength value also dropped. None of this is diagnostic; it is a reason to measure body composition before the next dose step.
System verdict
Review
Organ response index −0.9× noise band · 11 proteins · 0 moved / 7 unchanged / 4 review
IGF1 Insulin-like growth factor 1Clinic grip strength 26 → 24 kg
Review142 → 118 ng/mL · −17% · 1.9× noise
IGFBP3 Insulin-like growth factor-binding protein 3
Unchanged3.8 → 3.4 µg/mL · −11% · 1.3× noise
FSTL3 Follistatin-related protein 3Rises with catabolic signalling
Review9.8 → 12.4 ng/mL · +27% · 2.4× noise
CKM Creatine kinase M-typeMuscle-leak protein; also falls with less training
Unchanged120 → 96.0 ng/mL · −20% · 0.9× noise
MB Myoglobin
Unchanged32.0 → 29.0 ng/mL · −9% · 0.5× noise
FABP3 Fatty acid-binding protein, heart
Unchanged2.1 → 2.0 ng/mL · −5% · 0.3× noise
GDF11 Growth/differentiation factor 11
Unchanged168 → 171 pg/mL · +2% · 0.1× noise
SOST SclerostinSclerostin; rises with unloading
Review380 → 462 pg/mL · +22% · 1.8× noise
ACP5 Tartrate-resistant acid phosphatase type 5TRAP5b, bone resorption
Review2.8 → 3.4 ng/mL · +21% · 1.6× noise
TNFRSF11B Tumor necrosis factor receptor superfamily member 11BOsteoprotegerin
Unchanged4,200 → 4,380 pg/mL · +4% · 0.4× noise
PTH Parathyroid hormone
Unchanged42.0 → 47.0 pg/mL · +12% · 0.7× noise
Trajectory shows Baseline → Week 4 → Week 8 → Week 12. “Vs noise” is the Week 12 change divided by this patient’s expected within-person variation for that protein. Changes under 1.5× are reported as unchanged. The noise is the technical replicates on the same plate plus cohort within-person variance. Concentrations are calibrant-relative values from dried capillary blood and are not interchangeable with venous clinical assays of the same analyte.
Response by SuperOmeGut barrier & mucosa
M.K. · R-0417 · GLP-1 initiation (semaglutide)
Gut barrier & mucosa
Intestinal fatty-acid binding protein rose during the weeks nausea was reported and had not fully settled by Week 12. Endotoxin-exposure markers drifted down but stayed inside the noise band. Worth re-checking after the dose has been stable for four weeks.
System verdict
Review
Organ response index −0.1× noise band · 7 proteins · 0 moved / 6 unchanged / 1 review
FABP2 Fatty acid-binding protein, intestinalI-FABP; enterocyte turnover
Review1.4 → 1.9 ng/mL · +36% · 2.2× noise
LBP Lipopolysaccharide-binding protein
Unchanged8.2 → 7.1 µg/mL · −13% · 1.2× noise
CD14 Monocyte differentiation antigen CD14Soluble CD14
Unchanged1.62 → 1.51 µg/mL · −7% · 0.8× noise
REG3A Regenerating islet-derived protein 3-alphaMucosal repair / antimicrobial
Unchanged60.0 → 72.0 ng/mL · +20% · 1.2× noise
REG1B Lithostathine-1-beta
Unchanged18.0 → 21.0 ng/mL · +17% · 0.9× noise
TFF3 Trefoil factor 3
Unchanged12.1 → 12.9 ng/mL · +7% · 0.6× noise
REG4 Regenerating islet-derived protein 4
Unchanged3.1 → 3.0 ng/mL · −3% · 0.2× noise
Trajectory shows Baseline → Week 4 → Week 8 → Week 12. “Vs noise” is the Week 12 change divided by this patient’s expected within-person variation for that protein. Changes under 1.5× are reported as unchanged. The noise is the technical replicates on the same plate plus cohort within-person variance. Concentrations are calibrant-relative values from dried capillary blood and are not interchangeable with venous clinical assays of the same analyte.
Response by SuperOmeBrain & neuro
M.K. · R-0417 · GLP-1 initiation (semaglutide)
Brain & neuro
Neuro-injury markers were unchanged. Neurofilament light reads close to the assay's quantification limit in dried capillary blood, so small changes should not be interpreted; BDNF drifted up but stayed inside the noise band.
System verdict
Unchanged
Organ response index +0.4× noise band · 5 proteins · 0 moved / 5 unchanged / 0 review
NEFL Neurofilament light polypeptideNear LLOQ; interpret with caution
Unchanged9.2 → 9.0 pg/mL · −2% · 0.1× noise
GFAP Glial fibrillary acidic protein
Unchanged85.0 → 82.0 pg/mL · −4% · 0.2× noise
BDNF Neurotrophic factor BDNF precursor form
Unchanged22.1 → 25.4 ng/mL · +15% · 1.2× noise
GRN ProgranulinProgranulin
Unchanged41.0 → 40.0 ng/mL · −2% · 0.3× noise
APOE Apolipoprotein E
Unchanged38.0 → 39.0 µg/mL · +3% · 0.3× noise
Trajectory shows Baseline → Week 4 → Week 8 → Week 12. “Vs noise” is the Week 12 change divided by this patient’s expected within-person variation for that protein. Changes under 1.5× are reported as unchanged. The noise is the technical replicates on the same plate plus cohort within-person variance. Concentrations are calibrant-relative values from dried capillary blood and are not interchangeable with venous clinical assays of the same analyte.
Response by SuperOmeFor the visit
M.K. · R-0417
What to discuss, what to measure next, what this report does not do.
Suggested discussion points
- Lean mass. IGF-1 down 17%, FSTL3 up 27%, sclerostin and TRAP5b up, grip strength 26 → 24 kg, 7.7 kg lost in 12 weeks. Consider DXA (or BIA if DXA is unavailable) before stepping to 1.7 mg; protein intake ≥ 1.2 g/kg and resistance training 2–3×/week.
- Gut epithelium. I-FABP rose during the nausea weeks and had not returned to baseline by Week 12. Re-check once the dose has been stable for four weeks. If GI symptoms return at the next step, this is the marker to watch.
- Metabolic response is strong. Fasting insulin, C-peptide, leptin, FGF21 and FABP4 all fell; adiponectin and IGFBP-1 rose. HbA1c is now below the prediabetes threshold.
- GDF15 drifted up but stayed inside the noise band. Common on metabolic drugs; no action, re-measure.
Next measurement window
Week 16–18 · one home sample, after ≥ 4 weeks at a stable dose.
The next sample will be run with this patient's reserved baseline aliquot on the same plate, so the comparison stays within one calibrator lot.
Questions the patient may ask
- "Is my liver better?" — ALT and liver-fat proteins fell; fibrosis markers were unchanged, which is expected at 12 weeks.
- "Am I losing muscle?" — The pattern is consistent with it; a scan answers it.
- "Is my heart OK?" — Endothelial markers improved; troponin and NT-proBNP from the clinic lab are normal.
What this report does not do
It does not diagnose. Proteomic values are Research Use Only. Any result that would change management should be confirmed with an accredited clinical test.
It does not report a biological age. No published proteomic clock is valid on this platform without re-calibration, so none is shown. Organ response indices are within-patient, sign-and-magnitude readouts.
It does not compare patients. Every flag is relative to this patient's own baseline and noise. Population reference intervals are shown only for the accredited clinical values.
Companion. The patient can ask the companion about any line in this report in plain language. The companion explains and prepares questions; it does not change doses. Anything requiring a medical decision is routed back to the ordering clinician.
Response by SuperOmeMethods & appendix
M.K. · R-0417
How this report was produced
- Platform
- Multiplex proteomics panel v2.1 · about 1,000 assays · quantification against recombinant standard curves (16-point, 4PL) run on a calibration plate the same day.
- Specimen
- Capillary whole blood, volumetric tips (20 µL), air-dried and stored at room temperature; four samples returned together at Week 12. Eluted per the panel's protocol (150 µL buffer per tip, 1 h, protease inhibitor).
- Batching
- All four timepoints for this patient on one plate, same bead lot, same calibrator lot, same run. One aliquot per timepoint held in reserve at −80 °C.
- Noise band
- Per-protein within-person SD estimated from on-plate technical replicates and cohort baseline variance ("borrowed noise"). A change is reported when it exceeds 1.5× that SD; the direction is then compared to the program's intended direction.
- Detectability
- 781 assays were above LLOQ in all four of this patient's samples and are eligible for reporting; 92 were quantifiable in some timepoints only; 190 were below LLOQ throughout (predominantly intracellular proteins, expected in dried capillary blood).
- Sample QC
- All four samples passed: haemolysis index low (4 / 4), dwell time 1–84 days recorded, reference sample co-shipped and within tolerance.
- Regulatory
- Research Use Only. Not CLIA-returnable. Clinical anchors from an accredited laboratory.
Largest whole-panel movers outside the curated panels
Of the proteins not shown on the organ pages, these moved most relative to the patient's own noise. Exploratory; included so nothing large is hidden by panel curation. Detect = timepoints above LLOQ.
| Gene | protein | Δ Wk12 | Vs noise | Detect |
|---|---|---|---|---|
| CSF3 | Granulocyte colony-stimulating factor | +42% | 4.9× | 3/4 |
| GPR158 | Metabotropic glycine receptor | +47% | 4.7× | 3/4 |
| GPX1 | Glutathione peroxidase 1 | −47% | 4.7× | 4/4 |
| RGMA | Repulsive guidance molecule A | −47% | 4.1× | 3/4 |
| HSPA8 | Heat shock cognate 71 kDa protein | −46% | 3.8× | 4/4 |
| SULT2A1 | Sulfotransferase 2A1 | −47% | 3.7× | 3/4 |
| DLK1 | Protein delta homolog 1 | +39% | 3.6× | 4/4 |
| SOD1 | Superoxide dismutase [Cu-Zn] | −29% | 3.2× | 4/4 |
| IL6R | Interleukin-6 receptor subunit alpha | −25% | 2.9× | 4/4 |
| AOC1 | Diamine oxidase | +27% | 2.6× | 3/4 |
| TNFRSF25 | Tumor necrosis factor receptor superfamily member 25 | −44% | 2.6× | 3/4 |
| GZMA | Granzyme A | −41% | 2.3× | 4/4 |
| CEACAM19 | Cell adhesion molecule CEACAM19 | −30% | 2.1× | 4/4 |
| DBH | Dopamine beta-hydroxylase | +37% | 2.1× | 4/4 |
| SDC3 | Syndecan-3 | +30% | 2.0× | 3/4 |
| FAS | Tumor necrosis factor receptor superfamily member 6 | +28% | 2.0× | 4/4 |
| CLEC5A | C-type lectin domain family 5 member A | −32% | 1.9× | 4/4 |
| SELP | P-selectin | +22% | 1.9× | 3/4 |
| IL7 | Interleukin-7 | −26% | 1.8× | 4/4 |
| FCGR3A | Low affinity immunoglobulin gamma Fc region receptor III-A | +34% | 1.8× | 4/4 |
Within-person CV, LLOQ and detectability come from the per-target validation table of the platform. Gene symbols are the assay identifiers of the panel.