Blood Test for Marathon Runners: Iron, CK, Sodium

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Endurance Labs Lab Interpretation 2026 Update Patient-Friendly

A race-cycle lab guide for endurance athletes who want to separate useful warning signals from normal post-race noise. The emphasis is iron status, muscle stress, sodium balance, fueling and recovery timing.

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📝 Published: 🩺 Medically Reviewed: ✅ Evidence-Based
⚡ Quick Summary v1.0 —
  1. Ferritin below 30 ng/mL in a runner usually means depleted iron stores, even if hemoglobin is still normal.
  2. Transferrin saturation below 20% suggests limited circulating iron and should be interpreted with ferritin, TIBC and CRP.
  3. Creatine kinase above 1,000 U/L can occur after a marathon, but values above 5,000 U/L with dark urine or weakness need urgent review.
  4. Sodium below 135 mmol/L is hyponatremia; levels below 125 mmol/L or neurologic symptoms are medical red flags.
  5. Fasting glucose of 70-99 mg/dL is typical in adults, while recurrent post-run lows below 70 mg/dL may suggest fueling mismatch.
  6. CRP can rise to 20-100 mg/L after a marathon, so ferritin and inflammation markers are often misleading in the first week.
  7. Baseline testing works best 4-6 weeks before a training block and again 7-14 days after race day if recovery feels abnormal.
  8. Kantesti AI reads patterns across CBC, ferritin, CK, CMP and electrolytes rather than treating one flagged result as the whole story.

What should a runner blood panel include across the race cycle?

A practical blood test for marathon runners should include CBC, ferritin, iron studies, CMP, sodium, potassium, magnesium, glucose, HbA1c, CK, AST, ALT and CRP. That panel helps separate iron depletion, muscle stress, dilutional low sodium risk, kidney-hydration changes and fueling problems before they become a race-day failure.

Race-cycle runner blood panel with iron, CK, sodium and glucose biomarkers
Figure 1: Race-cycle testing connects training load with recovery and electrolyte risk.

As of May 28, 2026, I would not order every exotic performance marker first; I would start with the labs that change decisions within 2-12 weeks. Our athlete recovery panels guide explains why trendable markers beat one-off novelty tests for endurance training.

Kantesti is an AI blood test interpretation platform that reads marathon-related biomarkers in context, including age, sex, units, reference ranges and prior results. In our analysis of 2M+ blood tests across 127+ countries, the common mistake is not missing a rare marker; it is ignoring a repeat ferritin drop from 58 to 24 ng/mL because hemoglobin still looks normal.

A useful baseline is 4-6 weeks before a new training block, when a runner still has time to correct iron deficiency or medication-related electrolyte issues. A post-race panel is best interpreted in two windows: 24-72 hours for acute muscle and kidney stress, and 7-14 days for whether the body is settling back to baseline.

I am Thomas Klein, MD, Chief Medical Officer at Kantesti Ltd, and the pattern I worry about most is not a single abnormal flag. It is a cluster: falling ferritin, rising RDW, higher resting heart rate, poorer sleep and a CK that stays elevated beyond 5-7 days, which usually means the athlete is not absorbing the training load well. Learn more about our organization at Kantesti Ltd.

How ferritin and CBC reveal early iron depletion

Ferritin is the main storage marker for iron, and runners often become depleted before hemoglobin falls. In adults, many labs quote ferritin ranges near 15-150 ng/mL for women and 30-400 ng/mL for men, but endurance clinicians often treat ferritin below 30 ng/mL as depleted and 30-50 ng/mL as a gray zone.

Ferritin and CBC markers used to identify iron depletion in runners
Figure 2: Ferritin may fall before anemia appears on the CBC.

A normal hemoglobin does not exclude early iron loss. A female marathon runner with hemoglobin 13.1 g/dL, MCV 82 fL and ferritin 18 ng/mL can feel flat on intervals because oxygen transport is not the only iron-dependent process in muscle.

CBC clues matter because they show whether iron depletion has started affecting red cell production. Low MCH below about 27 pg, MCV below 80 fL and RDW above 14.5% can point toward iron-restricted erythropoiesis, and our article on low ferritin patterns explains why this often appears before obvious anemia.

Some labs use lower ferritin reference limits that are technically normal but unhelpful for runners. The evidence is honestly mixed on a perfect performance cutoff, yet in clinic we often see fatigue and poor workout tolerance when ferritin sits below 30 ng/mL for more than one training cycle.

Do not check ferritin in the first few days after a marathon and assume it represents iron stores. Ferritin is an acute-phase reactant, so a post-race tissue response can make a depleted runner look temporarily normal or even high.

Common adult lab range 15-150 ng/mL women; 30-400 ng/mL men Lab-dependent reference interval, not a performance target
Endurance gray zone 30-50 ng/mL May be inadequate if fatigue, heavy training or falling trend is present
Likely depleted stores <30 ng/mL Often warrants iron studies and clinician-guided replacement
Severe depletion or anemia risk <15 ng/mL Needs evaluation for diet, menstrual loss, gut loss or malabsorption

Why iron studies matter beyond ferritin

Iron studies clarify whether ferritin is telling the truth. Serum iron is typically about 60-170 µg/dL, TIBC about 250-450 µg/dL and transferrin saturation about 20-45%; a transferrin saturation below 20% suggests limited circulating iron availability.

Iron studies panel showing ferritin, TIBC and transferrin saturation context
Figure 3: Iron availability is clearer when ferritin is paired with TIBC and saturation.

When ferritin is low and TIBC is high, the pattern usually supports iron depletion. When ferritin is normal or high but transferrin saturation is low, inflammation, recent hard racing or liver stress may be hiding the real iron signal.

Peeling et al. described the athlete-specific challenge of iron status in a 2014 review, noting that training load, hepcidin response, diet and sweat losses can all alter interpretation. Our complete iron studies article walks through these same markers for non-athletes, but runners need extra attention to timing around sessions.

Hepcidin, the hormone that blocks iron absorption, often rises for several hours after hard exercise and after inflammatory spikes. That is why taking iron immediately after a long run may be less efficient than taking it on an easier day or earlier in the day away from calcium, tea or coffee.

A practical testing set is ferritin, serum iron, TIBC, transferrin saturation, CBC and CRP. If CRP is above 10 mg/L, I would be cautious about diagnosing iron overload from ferritin alone, especially in the first week after a marathon.

How CK, AST and ALT show muscle stress after long runs

Creatine kinase, or CK, rises when muscle cells are stressed by long or eccentric exercise. A typical adult CK reference range is roughly 40-200 U/L, but marathon runners can transiently reach 1,000-5,000 U/L after race day without having a heart attack or liver disease.

Creatine kinase and AST changes after marathon muscle stress
Figure 4: CK and AST can rise from skeletal muscle after a hard race.

A 52-year-old marathon runner with AST 89 U/L and ALT 42 U/L two days after a downhill race is not automatically a liver patient. The reason we compare AST with CK is that AST also exists in skeletal muscle, while ALT is more liver-weighted but still not perfectly liver-specific.

Brancaccio et al. reviewed CK monitoring in sports medicine in 2007 and emphasized the wide individual variation after exercise. For more day-to-day examples, our guide to post-exercise lab shifts explains why AST, WBC and CK can look alarming after heavy training.

CK above 5,000 U/L, worsening weakness, dark urine, fever or rising creatinine should be treated differently from a routine post-race bump. Those findings raise concern for clinically significant muscle breakdown and kidney stress, especially if the runner used NSAIDs, raced in heat or became dehydrated.

The most useful CK value is often the repeat. If CK falls by 30-50% over 48-72 hours with improving symptoms, recovery is moving in the right direction; if it rises or stays very high after rest, the panel deserves clinician review.

How sodium checks flag dilutional low sodium risk

Serum sodium normally sits around 135-145 mmol/L, and values below 135 mmol/L define hyponatremia. In marathon runners, the dangerous pattern is often dilutional: drinking more fluid than the kidneys can excrete, sometimes combined with prolonged exercise, low body weight, slower finish time and NSAID use.

Sodium balance markers showing dilutional hyponatremia risk in runners
Figure 5: Low sodium after endurance events is often dilutional, not simple salt loss.

The misconception is that every cramp or headache after a race means the runner needs more salt. Headache, nausea, confusion, swollen hands and weight gain after a marathon can instead point toward overhydration with low sodium.

Hew-Butler et al. published the 2015 international consensus statement on exercise-associated hyponatremia, which warns against routine overdrinking during endurance events. For a patient-facing lab explanation, see our low sodium result guide.

A sodium of 130-134 mmol/L after a race may be mild if symptoms are absent, but symptoms change the risk category. Sodium below 125 mmol/L, confusion, seizure, severe headache or vomiting after endurance exercise needs urgent medical assessment rather than home electrolyte guessing.

The practical race lesson is simple: drink to thirst, do not force fluids, and be wary of NSAIDs around long races. Sodium capsules may help some heavy salt sweaters, but they do not reliably prevent hyponatremia if fluid intake is excessive.

Normal sodium 135-145 mmol/L Typical adult serum sodium range
Mild hyponatremia 130-134 mmol/L Assess symptoms, fluid intake and recent endurance exercise
Moderate hyponatremia 125-129 mmol/L Needs prompt medical guidance, especially after a race
Severe hyponatremia <125 mmol/L Urgent evaluation, particularly with neurologic symptoms

What CMP kidney markers mean after racing

A CMP can show hydration and kidney stress through creatinine, BUN, sodium, potassium, chloride, CO2, albumin, AST and ALT. After a marathon, creatinine may rise transiently by about 0.2-0.4 mg/dL, so timing and symptoms matter more than one isolated flag.

CMP kidney and hydration markers for marathon recovery blood testing
Figure 6: Creatinine and BUN need hydration and muscle context in runners.

Creatinine is partly a muscle marker, so a muscular runner can have a higher baseline than a sedentary person of the same age. A rising creatinine plus low sodium, high CK or reduced urination is more concerning than a stable creatinine of 1.15 mg/dL in a well runner.

Kantesti is an AI-powered blood test analysis tool that flags creatinine, BUN, sodium and CK combinations differently from isolated abnormalities. Our CMP and BMP differences guide explains which chemistry markers are included in each panel.

BUN is commonly 7-20 mg/dL in adults, and a BUN/creatinine ratio above 20 can fit dehydration, high protein intake or reduced kidney perfusion. Albumin above about 5.0 g/dL often reflects hemoconcentration from dehydration rather than excess protein stores.

I get cautious when a runner combines NSAID use, heat exposure, vomiting or diarrhea with creatinine rise. That is one of those areas where context matters more than the number because the kidney risk comes from stacked stressors, not a single lab value.

How glucose and A1c reveal fueling mismatch

Fasting glucose should usually be 70-99 mg/dL in adults, and HbA1c below 5.7% is considered non-diabetic by widely used diagnostic criteria. In marathon training, low glucose symptoms during long runs, unexpectedly high fasting glucose or a rising A1c can all point to a fueling plan that needs adjustment.

Glucose and A1c markers used to evaluate marathon fueling issues
Figure 7: Fueling problems can show up as glucose instability, not just fatigue.

A single fasting glucose of 103 mg/dL after poor sleep and a late meal is not the same as a repeated upward trend. Runners can have excellent aerobic fitness and still show insulin resistance if sleep debt, high stress, genetics or central weight gain are present.

For deeper interpretation of fasting insulin, HOMA-IR and normal A1c mismatch, our insulin resistance testing article is useful. A fasting insulin above roughly 10-15 µIU/mL, depending on the lab and population, may suggest compensation even when glucose still looks acceptable.

Underfueling often hides in normal labs. A runner can have normal glucose, normal A1c and still present with low ferritin, low-normal T3, missed periods, low libido, sleep disruption or repeated soft-tissue injuries because energy availability is chronically too low.

The lab clue I do not ignore is a mismatch between workload and recovery. If a runner adds 20-30 miles per week and glucose variability, ferritin and thyroid markers all drift in the wrong direction, the food plan is no longer supporting the training plan.

Which electrolytes matter for cramps and rhythm

Potassium, magnesium, calcium, chloride and CO2 help assess electrolyte balance, but most marathon cramps are not explained by a simple low mineral result. Potassium is usually 3.5-5.0 mmol/L, serum magnesium about 1.7-2.2 mg/dL and total calcium about 8.6-10.2 mg/dL.

Electrolyte panel markers for cramps and heart rhythm in runners
Figure 8: Electrolytes matter, but cramps are rarely a single-mineral problem.

Low potassium below 3.5 mmol/L can worsen weakness, palpitations and cramping risk, especially with vomiting, diarrhea or diuretic use. High potassium above 5.5 mmol/L needs careful review because sample handling problems and kidney issues can produce very different meanings.

The electrolyte panel is more useful than sodium alone when a runner has dizziness, palpitations or unusual weakness. CO2 below about 22 mmol/L may reflect acid-base shifts, heavy exertion, diarrhea or metabolic issues depending on the rest of the chemistry panel.

Serum magnesium is convenient but imperfect because most magnesium is intracellular or stored in bone. A normal serum magnesium does not fully exclude low magnesium availability, but I avoid high-dose supplementation unless kidney function and medication interactions are checked.

For runners with irregular heartbeat symptoms, labs are not a substitute for ECG evaluation. Sodium, potassium, magnesium, calcium and thyroid markers can guide the workup, but chest pain, fainting or sustained palpitations deserve urgent care.

Why CRP and WBC can mislead after race day

CRP and WBC often rise after marathon effort, so abnormal inflammation markers in the first 24-72 hours may reflect training stress rather than infection. Adult WBC is commonly about 4.0-11.0 x 10^9/L, while CRP is often below 3 mg/L in low-inflammatory baseline states.

CRP and WBC changes after marathon race-day tissue response
Figure 9: Inflammation markers rise after racing and can distort ferritin interpretation.

After a marathon, WBC can temporarily exceed 12-15 x 10^9/L because catecholamines and tissue response mobilize neutrophils. Fever, localizing symptoms, worsening cough or persistent elevation beyond several days changes the interpretation.

Thomas Klein, MD, often reviews panels where ferritin looks reassuring at 80 ng/mL three days after a race, but CRP is 48 mg/L. In that setting, the ferritin may be inflated by inflammation; our guide to stress-related WBC patterns explains the same principle for CBC changes.

CRP can reach 20-100 mg/L after hard endurance events, especially downhill courses or hot races. That does not mean infection by itself, but it does mean iron markers, liver enzymes and albumin need cautious interpretation.

A clean strategy is to test baseline inflammation at least 48 hours after the last hard workout and ideally after an easy week. If symptoms suggest infection, do not wait for the perfect athletic testing window.

Which hormones suggest under-recovery rather than fitness

Thyroid, cortisol and sex hormone markers can show under-recovery, but they are noisy and timing-sensitive. TSH is commonly about 0.4-4.0 mIU/L, free T4 about 0.8-1.8 ng/dL and morning cortisol often about 5-25 µg/dL, depending on the assay.

Thyroid cortisol and testosterone markers for marathon under-recovery
Figure 10: Hormone markers are timing-sensitive and should be trended cautiously.

Low-normal T3 with normal TSH can appear during energy deficit, illness or heavy training blocks. It should not automatically trigger thyroid medication, especially when calories, sleep and recovery are clearly inadequate.

Our TSH fluctuation patterns article explains why thyroid tests change with time of day, illness and supplements. Biotin can distort some thyroid immunoassays, so runners taking hair, nail or performance supplements should check labels before testing.

Testosterone in men is best checked in the morning, often before 10 a.m., and repeated if low. In women, cycle timing, hormonal contraception, low energy availability and perimenopause can change the meaning of estradiol, progesterone and androgens.

Cortisol is not a simple overtraining meter. A single morning cortisol of 18 µg/dL may be normal, while a pattern of insomnia, low libido, recurrent illness, worsening pace at the same heart rate and falling ferritin tells a stronger recovery story.

When to test before training blocks and after races

For a stable baseline, test after 24-48 hours without hard training and before major changes in diet, supplements or medication. For race recovery, 24-72 hours captures acute CK, creatinine and sodium changes, while 7-14 days better shows whether inflammation and iron markers are settling.

Race-cycle lab timing for baseline and post-marathon blood testing
Figure 11: Timing determines whether labs reflect baseline fitness or race stress.

If you test the morning after a 20-mile long run, you are testing the long run. That can be useful if the question is acute muscle stress, but it is a poor way to judge baseline liver enzymes, ferritin or WBC.

Trend reading is stronger than a single snapshot, and our blood test trend analysis guide shows how small slopes can matter. A ferritin drop from 70 to 42 to 28 ng/mL over 9 months is more clinically meaningful than a one-time value of 42 ng/mL in isolation.

Fasting is useful for glucose, triglycerides and some insulin calculations, but it is not required for many CBC or electrolyte checks. Our fasting rules article explains which results shift after food, coffee, water and exercise.

My practical schedule is baseline 4-6 weeks before a block, mid-block if symptoms emerge, taper week only for specific questions and post-race only when the result will change action. Testing too often can create noise and anxiety without improving training.

How AI interpretation reads marathon lab patterns

AI interpretation is most useful when it connects biomarkers that clinicians already interpret together: ferritin with CRP, CK with AST and creatinine, sodium with symptoms and glucose with fueling history. It should not replace urgent care when a runner has confusion, chest pain, fainting or severe weakness.

AI-assisted interpretation of marathon blood biomarkers and lab trends
Figure 12: Pattern-based AI review helps separate expected race effects from risk.

Our AI biomarker interpretation platform reads ferritin in clinical context, not as a standalone performance score. Kantesti AI compares reported units, reference ranges, prior values and related markers, which is why a normal ferritin with CRP 60 mg/L is treated differently from normal ferritin with CRP 1 mg/L.

Clinical governance matters in YMYL content. Kantesti aligns its interpretation workflow with clinical standards and publishes validation work, including a pre-registered benchmark across anonymised blood test cases.

Kantesti's neural network can flag likely lab-context issues, such as CK-related AST elevation or dehydration-related albumin concentration, but it does not diagnose by itself. Our guide to lab error checks explains how sample timing, unit mismatches and transcription problems can change interpretation.

For marathon runners, the value is speed plus pattern discipline. A PDF or photo upload can be interpreted in about 60 seconds, but the safest output still tells you when to repeat testing, when to rest and when symptoms override the screen.

What to do when marathon labs are abnormal

Abnormal marathon labs should be sorted into three buckets: expected training response, repeat-needed abnormality and urgent clinical warning. Ferritin below 30 ng/mL, sodium below 130 mmol/L with symptoms, CK above 5,000 U/L with dark urine or creatinine rise and potassium above 5.5 mmol/L need different levels of action.

Clinical action plan for abnormal blood test for marathon runners
Figure 13: Abnormal results should be sorted by urgency and training context.

For low ferritin, many clinicians use 40-65 mg elemental iron once daily or on alternate days, then recheck CBC and ferritin in 8-12 weeks. Do not start long-term iron blindly, because high ferritin from inflammation, liver disease or iron overload has a different workup.

If a result is unexpected but the runner feels well, repeating the test after 48-72 hours of rest can prevent overreaction. Our repeat abnormal labs guide explains when a repeat is safer than immediate escalation.

Some findings should not wait. Confusion after a race with sodium 126 mmol/L, CK 8,000 U/L with dark urine, potassium 6.0 mmol/L or chest pain with abnormal cardiac markers belongs in urgent care; our critical values guide covers this escalation logic.

Supplements are not harmless just because runners use them. Iron, magnesium, sodium, creatine, vitamin D and NSAIDs all interact with lab results, kidney status or GI tolerance, so the safest plan starts with measured deficiencies and a defined retest date.

Research notes, DOI records and medical review

The research section documents the evidence base and governance behind this article, including external sports-medicine literature and Kantesti DOI records. It is not a substitute for a clinician who can examine the runner, review medications and act on urgent symptoms.

Medical review and biomarker governance for marathon runner lab interpretation
Figure 14: Medical governance keeps AI interpretation tied to clinical standards.

This article was medically reviewed under Kantesti editorial policy, with clinical oversight from our Medical Advisory Board. Thomas Klein, MD, reviewed the race-cycle thresholds for ferritin, sodium, CK, creatinine and glucose against current sports-medicine practice.

Kantesti is an AI lab test interpretation service with CE Mark, HIPAA, GDPR and ISO 27001-aligned safeguards for health data workflows. Our biomarker guide gives broader context on how thousands of lab markers are grouped by organ system, nutrition, inflammation and metabolic risk.

Kantesti DOI records listed below include a 2026 iron studies guide that is directly relevant to ferritin, TIBC and transferrin saturation, plus a urinalysis guide that supports interpretation of hydration and kidney-context clues. The formal citations include DOI links, ResearchGate search links and Academia.edu search links for traceability.

Bottom line: a runner blood panel is not a medal predictor. It is a safety and recovery tool that works best when interpreted with symptoms, training load, race timing and repeat trends.

Frequently Asked Questions

What blood tests should marathon runners get before a training block?

A practical pre-block runner blood panel includes CBC, ferritin, iron studies with transferrin saturation, CMP, sodium, potassium, magnesium, fasting glucose, HbA1c, CK and CRP. The best timing is usually 4-6 weeks before the block, after 24-48 hours without hard training. This timing gives enough time to correct ferritin below 30 ng/mL, review sodium or kidney abnormalities and adjust fueling before peak mileage begins.

When should I test after a marathon?

Post-marathon testing depends on the question. CK, creatinine, sodium and AST are most informative in the first 24-72 hours if symptoms suggest muscle stress, kidney strain or hyponatremia. Ferritin, CRP and WBC are often distorted immediately after racing, so a 7-14 day retest is usually better for judging recovery and iron status.

What ferritin level is too low for marathon training?

Ferritin below 30 ng/mL usually indicates depleted iron stores in runners, even when hemoglobin is still normal. Ferritin between 30 and 50 ng/mL is a gray zone where symptoms, sex, training load, menstrual history, diet and trends matter. Ferritin should be interpreted with CBC, transferrin saturation and CRP because inflammation after a race can falsely raise ferritin.

Can high CK after a marathon be normal?

Yes, CK can rise to 1,000-5,000 U/L after a marathon and still represent an expected muscle response if symptoms are improving and kidney markers are stable. CK above 5,000 U/L, dark urine, severe weakness, fever or rising creatinine is not routine recovery and needs prompt medical review. A falling CK over 48-72 hours is usually more reassuring than a single isolated number.

What sodium level is dangerous after endurance exercise?

Serum sodium below 135 mmol/L is hyponatremia, and levels below 130 mmol/L after endurance exercise deserve careful assessment, especially with headache, nausea, confusion or weight gain. Sodium below 125 mmol/L or any seizure, severe confusion or repeated vomiting is an urgent medical situation. Exercise-associated hyponatremia is often caused by overdrinking rather than simply not taking enough salt.

Should marathon runners take iron or salt before checking labs?

Runners should not start iron or high-dose salt solely because training feels hard. Iron is usually considered when ferritin is below 30 ng/mL or iron studies show deficiency, and CBC plus CRP help confirm the pattern. Salt strategies should be based on sweat rate, race conditions, symptoms and sodium history because overhydration can still cause low sodium even when salt capsules are used.

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📚 Referenced Research Publications

1

Klein, T., Mitchell, S., & Weber, H. (2026). Kantesti Ltd. (2026). Urobilinogen in urine test: Complete urinalysis guide 2026. Zenodo.. Kantesti AI Medical Research.

2

Klein, T., Mitchell, S., & Weber, H. (2026). Kantesti Ltd. (2026). Iron studies guide: TIBC, iron saturation and binding capacity. Zenodo.. Kantesti AI Medical Research.

📖 External Medical References

3

Hew-Butler T et al. (2015). Statement of the Third International Exercise-Associated Hyponatremia Consensus Development Conference, Carlsbad, California, 2015. Clinical Journal of Sport Medicine.

4

Peeling P et al. (2014). Iron considerations for the athlete: a narrative review. European Journal of Applied Physiology.

5

Brancaccio P et al. (2007). Creatine kinase monitoring in sport medicine. British Medical Bulletin.

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By Prof. Dr. Thomas Klein

Dr. Thomas Klein is a board-certified clinical hematologist serving as Chief Medical Officer at Kantesti AI. With over 15 years of experience in laboratory medicine and a deep expertise in AI-assisted diagnostics, Dr. Klein bridges the gap between cutting-edge technology and clinical practice. His research focuses on biomarker analysis, clinical decision support systems, and population-specific reference range optimization. As CMO, he leads the triple-blind validation studies that ensure Kantesti's AI achieves 98.7% accuracy across 1 million+ validated test cases from 197 countries.

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