Dr. L Chetan Reddy, MD Doctor · Scientist · Innovator

Building the future of
preventive healthcare

Metabolic and hormonal risk, caught long before it becomes disease — with testing chosen for your case, and results explained in language you can actually act on.

MDUzhhorod · Best Graduate
ECFMGCertified 2022
4PubMed Papers
TDFGeneral Secretary

Registrations & Credentials

Trained, certified and recognised across three medical councils.

MDUzhhorod National University · Best Graduate
ECFMGCertified 2022
NMCNational Medical Commission, India
TSMCTelangana State Medical Council
ACC · AHAResearch presented

Knowledge Lab

The markers, and what each one is for.

Twenty-two measurements that carry most of the signal in preventive and metabolic work. Search or filter by system to see what each one measures and why it earns its place on a panel.

Knowledge Lab

The markers, and what each one is for.

Twenty-two measurements that carry most of the signal in preventive and metabolic work. Search or filter by system, then open one to see what it measures, why it earns its place on a panel, and how often it is worth repeating.

Drag to rotate · tap any marker to open it

Check a number from your report

Choose the marker, type the value from your lab report, and see which reference band it falls in. Nothing is stored or sent anywhere — it runs on your own phone.

Check a value against the reference

A single value is read alongside fasting glucose and your history.

What it measures
The proportion of haemoglobin that has glucose bound to it. Because red cells live about 120 days, it averages your glucose over that window rather than catching a single moment.
Why it matters
It is the single most useful number for spotting insulin resistance before it becomes diabetes, and it cannot be gamed by fasting the morning of the test.
Typical adult reference
Below 5.7% — normal · 5.7 to 6.4% — prediabetes · 6.5% or above — diabetes range
When it is retested
Twelve weeks. Testing sooner tells you little, since the average has not had time to move.

Check a value against the reference

A diabetes-range value needs confirming on a second occasion.

What it measures
Plasma glucose measured after eight or more hours without food.
Why it matters
Paired with HbA1c it separates people whose glucose rises mainly after meals from those who are already running high at baseline.
Typical adult reference
70 to 99 mg/dL — normal · 100 to 125 — prediabetes · 126 or above on two occasions — diabetes range
When it is retested
With each panel. Twelve weeks after a change in protocol.

Check a value against the reference

Interpretation depends on the glucose measured with it — a normal glucose held up by a high insulin still matters.

What it measures
Circulating insulin in the fasted state, reported in µIU/mL.
Why it matters
Insulin rises years before glucose does. A normal glucose held up by a high insulin is the earliest stage of the problem, and it is invisible on a routine sugar test.
Typical adult reference
Assay-dependent, commonly 2 to 20 µIU/mL. Interpretation depends on the glucose measured alongside it, not the number alone.
When it is retested
Twelve to twenty-four weeks.

Check a value against the reference

Calculated from your fasting glucose and fasting insulin. Thresholds vary by population and assay.

What it measures
A calculation combining fasting glucose and fasting insulin into one index of how resistant tissues have become.
Why it matters
It turns two numbers into a single trend you can follow, which makes it easier to see whether an intervention is working.
Typical adult reference
Values under roughly 2.0 are generally considered favourable, though thresholds vary by population and assay.
When it is retested
Alongside insulin, twelve to twenty-four weeks.

Check a value against the reference

Measure at the midpoint between the lowest rib and the top of the hip bone, at the end of a normal breath out.

What it measures
Waist circumference divided by height — no equipment beyond a tape measure.
Why it matters
It flags central adiposity in people whose BMI reads normal, which matters especially in South Asian populations where metabolic risk appears at lower body weight.
Typical adult reference
Below 0.5 is the widely used target across adult heights and both sexes.
When it is retested
Every visit. It moves before the blood work does.

Check a value against the reference

Targets tighten considerably where cardiovascular risk is already established.

What it measures
One molecule of apolipoprotein B sits on every LDL, VLDL and Lp(a) particle, so measuring it counts the particles that can lodge in an artery wall.
Why it matters
Two people with identical LDL cholesterol can carry very different particle counts. ApoB resolves that, and tracks risk more closely than LDL-C where the two disagree.
Typical adult reference
Below about 90 mg/dL is a common general target; below 80 or lower where risk is already established.
When it is retested
Twelve weeks after any lipid intervention.

Check a value against the reference

Target depends on your overall risk, not on this number alone.

What it measures
The cholesterol content of low-density lipoprotein, usually calculated rather than measured directly.
Why it matters
The most established modifiable driver of atherosclerosis, and the marker most guidelines are still written around.
Typical adult reference
Below 100 mg/dL is generally considered optimal; targets fall substantially where cardiovascular risk is higher.
When it is retested
Twelve weeks.

Check a value against the reference

Check whether your report is in mg/dL or nmol/L — they are not interchangeable.

What it measures
A lipoprotein particle whose concentration is set mostly by genetics and stays broadly stable through life.
Why it matters
It is an independent risk factor that lifestyle barely shifts. Knowing it changes how aggressively everything else is treated — which is why it is worth measuring once.
Typical adult reference
Below roughly 50 mg/dL, or about 125 nmol/L, is commonly used as the threshold. Units differ between labs, so check which one your report uses.
When it is retested
Once in a lifetime is usually enough, unless there is a specific reason to repeat it.

Check a value against the reference

Must be drawn fasting. Alcohol in the preceding days will raise it.

What it measures
The main storage form of fat in blood, measured fasting.
Why it matters
It responds quickly to refined carbohydrate, alcohol and insulin resistance, which makes it one of the fastest-moving markers of whether a dietary change has landed.
Typical adult reference
Below 150 mg/dL — desirable · 150 to 199 — borderline · 200 or above — high
When it is retested
Six to twelve weeks. It moves faster than most.

Check a value against the reference

Read together with triglycerides rather than on its own.

What it measures
Cholesterol carried by high-density lipoprotein, involved in transporting it back out of tissues.
Why it matters
Useful in context and alongside triglycerides. Raising it with drugs has not reduced events, so it is read as a marker rather than a target in itself.
Typical adult reference
Above 40 mg/dL in men and above 50 mg/dL in women is the usual reference.
When it is retested
With each lipid panel.

Check a value against the reference

Invalid during or shortly after any infection, injury or flare.

What it measures
C-reactive protein measured with a high-sensitivity assay, sensitive enough to detect the low levels relevant to vascular risk.
Why it matters
Chronic low-grade inflammation compounds metabolic and cardiovascular risk. It also flags when something else is going on that the rest of the panel does not explain.
Typical adult reference
Below 1 mg/L — lower risk · 1 to 3 — average · above 3 — higher risk. Any recent infection or injury invalidates the reading.
When it is retested
Twelve weeks, and never during an acute illness.

Check a value against the reference

A raised value often points back to B12, folate or B6 rather than being the problem itself.

What it measures
An amino acid cleared using vitamin B12, folate and vitamin B6.
Why it matters
A raised value often points back to a B-vitamin gap rather than being the problem itself, which makes it a useful pointer when B12 sits in the borderline zone.
Typical adult reference
Below 15 µmol/L is the conventional reference; many clinicians prefer to see it under 10.
When it is retested
Twelve weeks after starting repletion.

Check a value against the reference

Reference shifts in pregnancy and with age. Read with free T4.

What it measures
Thyroid-stimulating hormone — the signal sent to the thyroid, which rises when the gland is underperforming.
Why it matters
Thyroid dysfunction mimics a great deal of what people attribute to metabolism, weight or mood, and it is cheap to rule in or out.
Typical adult reference
Roughly 0.4 to 4.0 mIU/L, though the upper limit is debated and shifts in pregnancy and with age.
When it is retested
Six to eight weeks after any dose change, otherwise annually.

Check a value against the reference

Assay-dependent — use the range printed on your own report where it differs.

What it measures
The fraction of thyroxine not bound to carrier proteins.
Why it matters
Read with TSH, it distinguishes a thyroid that is struggling from a pituitary signalling problem — two situations that need very different responses.
Typical adult reference
Approximately 0.8 to 1.8 ng/dL, assay-dependent.
When it is retested
With TSH.

Check a value against the reference

Adult male reference, morning draw. A single low result should be confirmed on a second sample.

What it measures
Total testosterone, drawn in the morning when levels peak.
Why it matters
Low testosterone and metabolic dysfunction drive each other in both directions, so it belongs in a metabolic work-up in men rather than being treated as a separate issue.
Typical adult reference
Roughly 300 to 1000 ng/dL in adult men. A single low morning result should always be confirmed on a second sample.
When it is retested
Confirm before acting; then as clinically indicated.

Check a value against the reference

For an 8–9 am draw only. Timing changes the result more than almost any other test.

What it measures
Serum cortisol drawn between 8 and 9 in the morning, when the daily rhythm is at its highest.
Why it matters
Sustained stress and disrupted sleep push glucose and central fat up through this axis, which is why sleep is treated as part of the metabolic protocol rather than an afterthought.
Typical adult reference
Approximately 6 to 23 µg/dL for a morning draw, assay-dependent. Timing matters more than almost any other test.
When it is retested
Only where the history points to it.

Check a value against the reference

25-hydroxyvitamin D. Repletion is usually rechecked at twelve weeks.

What it measures
25-hydroxyvitamin D, the circulating storage form that reflects intake and sun exposure over recent months.
Why it matters
Deficiency is common across India despite the sunlight, largely from indoor work and covering. It interacts with bone, muscle and immune function.
Typical adult reference
Below 20 ng/mL — deficient · 20 to 29 — insufficient · 30 to 100 — sufficient
When it is retested
Twelve weeks after starting repletion, then annually.

Check a value against the reference

In the borderline band, homocysteine helps decide whether it is genuinely low.

What it measures
Serum B12, best interpreted with homocysteine where the result is borderline.
Why it matters
Predominantly vegetarian diets and long-term metformin both deplete it. Deficiency presents as fatigue, tingling or fog long before anaemia appears — and the neurological damage is not always reversible if it is left.
Typical adult reference
Below 200 pg/mL — deficient · 200 to 300 — borderline, check homocysteine · above 300 — usually adequate
When it is retested
Twelve weeks after starting repletion.

Check a value against the reference

Rises with inflammation, so a normal value alongside a raised hs-CRP can still hide low iron.

What it measures
The storage protein for iron, which also rises as an acute-phase reactant during inflammation.
Why it matters
It is the earliest marker of iron depletion, and one of the most commonly missed causes of fatigue in menstruating women.
Typical adult reference
Roughly 30 to 300 ng/mL in men and 15 to 200 in women. Below 30 suggests depleted stores even where haemoglobin is still normal.
When it is retested
Twelve weeks after starting repletion, with hs-CRP to check inflammation is not inflating it.

Check a value against the reference

Healthy thresholds are argued to be lower than conventional lab limits.

What it measures
An enzyme released when liver cells are under stress.
Why it matters
Non-alcoholic fatty liver disease is largely silent, and a mildly raised ALT in someone with central adiposity is frequently the only clue before imaging.
Typical adult reference
Conventional upper limits sit near 33 U/L in women and 40 in men, though healthy thresholds are argued to be lower.
When it is retested
Twelve to twenty-four weeks.

Check a value against the reference

A reduced value must persist beyond three months before it means chronic kidney disease.

What it measures
Estimated glomerular filtration rate, calculated from creatinine with age and sex.
Why it matters
It sets the safety boundary for several medications and supplements, and it declines silently in long-standing diabetes and hypertension.
Typical adult reference
90 or above — normal · 60 to 89 — mildly reduced · below 60 sustained beyond three months — chronic kidney disease
When it is retested
Annually, or more often where diabetes or hypertension is established.

Check a value against the reference

Tracks with insulin resistance, fructose intake and alcohol.

What it measures
The end product of purine metabolism, cleared largely by the kidneys.
Why it matters
It tracks with insulin resistance, fructose intake and alcohol, and rising levels can precede gout by years.
Typical adult reference
Roughly 3.4 to 7.0 mg/dL in men and 2.4 to 6.0 in women.
When it is retested
Twelve to twenty-four weeks.
These are reference intervals, not a diagnosis. Ranges differ between laboratories, assays and populations, and a single value outside a range is often meaningless on its own — what matters is the pattern, the direction of travel and your history. Use this to understand a report you already hold, and bring it to a consultation rather than acting on it alone.

About

A route into medicine that started at the bedside.

I qualified as a nurse before I qualified as a doctor. Four years of B.Sc. Nursing, graduating as gold medallist, then medicine at Uzhhorod National University, where I finished as Best Graduating Student in Academics. I am the first doctor in my family.

That order matters more than it sounds. Nursing teaches you what happens to a patient in the twenty-three hours a day the doctor is not in the room — whether a plan is actually followable, and where it quietly fails.

Most patients arrive having already been told they are fine. That gap is where this practice works.

Training took me through internship at Osmania General Hospital, Hyderabad; a Medical Officer post at Sri Venkata Sai Medical College & Hospital; and a period teaching forensic medicine and toxicology at Mahabubnagar Government Medical College. In 2023 I completed clinical externships in Chicago, Houston and New York.

One question runs through all of it: what is actually causing this, and what would change it? It is why the clinic led to research, and why the research led to building.

B.Sc. Nursing

Gold Medallist

Four years of nursing training before medical school — the foundation the whole practice is built on.

MD · Uzhhorod

Best Graduating Student in Academics

ECFMG Certified 2022. First doctor in the family.

Internship

Osmania General Hospital, Hyderabad

Clinical grounding in one of the region's busiest teaching hospitals.

Medical Officer

Sri Venkata Sai Medical College & Hospital

Direct patient care across general and metabolic presentations.

Faculty

Mahabubnagar Government Medical College

Taught forensic medicine and toxicology alongside continuing clinical practice.

2023

Clinical Externships — Chicago, Houston, New York

Exposure to U.S. clinical systems and preventive-care models.

Doctor · Scientist · Innovator

One practice, three disciplines.

They are not separate jobs. The clinic decides what is worth researching, the research decides what is worth building, and what gets built comes back to the clinic. Select a card to turn it.

Clinical Focus

Where the work concentrates.

Three focus areas · drag to rotate · tap one

01 — Preventive medicine

Risk found while it is still cheap to fix

  • Cardiovascular risk stratification
  • Micronutrient deficiency, B12 & vitamin D
  • Sleep and circadian disruption
  • Family-history-led early screening
02 — Metabolic health

Insulin resistance and what precedes it

  • Prediabetes and type 2 diabetes
  • Dyslipidaemia and cardiovascular risk
  • Non-alcoholic fatty liver disease
  • Central adiposity at a lower BMI
03 — Endocrine contributors

Hormonal patterns that drive metabolic change

  • PCOS and androgen-driven symptoms
  • Thyroid dysfunction
  • Male hypogonadism, low testosterone
  • Perimenopausal metabolic change

Philosophy

Measure, then act. Then measure again.

Prevention fails when it stops at advice. It works when it becomes a loop, with numbers at both ends. Four stages, each with something you can hold.

The loop · drag to rotate · tap a stage

01

History before hypothesis

What you have lived, eaten, inherited and been prescribed. The pattern is usually already in the history; the tests confirm it.

02

Tests chosen, not bundled

Panels ordered for your presentation, then read to you in context — never a printout with values flagged and nothing explained.

03

The smallest effective change

Nutrition, movement, sleep and stress first. Medication where indicated. Supplementation only against a measured deficiency.

04

Verified, not assumed

Repeat measurement at fixed intervals. If the numbers have not moved, the protocol changes — not the patient's motivation.

Research & References

The reading behind the practice.

Four PubMed-indexed publications, with first authorship on nanotechnology applications in atherosclerosis, and poster presentations at the two principal international cardiology meetings.

2023

Nanotechnology in atherosclerosis

First author · Current Problems in Cardiology

PubMed-indexed
2023

Poster presentation

American College of Cardiology · Annual Scientific Session

Conference
2022

Poster presentation

American Heart Association · Scientific Sessions

Conference

Ecosystem

Two ventures, run separately.

Both exist because a clinical gap was easier to close by building than by prescribing around it. Neither is sold from this practice.

Founder

Nutrivance Clinical Sciences

Physician-formulated, condition-specific clinical nutrition — built for the gaps a prescription alone does not close, dosed the way the trials dosed it. Clinical collaboration with Dr. Vajja Pradeep.

Enquire about Nutrivance →
Co-founder

Truvantis Medtech

Sterile medical consumables manufactured in India to standards the operating room can rely on — because supply quality is a patient safety issue, not a procurement one.

Visit Truvantis Medtech →

The Programme

What happens, and when.

Every patient moves through the same four phases.

Four phases · drag to rotate · tap a phase

Week 0

Assessment

A 45-minute consultation covering metabolic, hormonal, medication and family history. Baseline measurements taken same day.

Weeks 0–2

Evidence

A baseline panel establishes where you stand. Additional panels ordered only where your history indicates them.

Week 2

Intervention

A written protocol — nutrition, movement, sleep, stress — with the reasoning behind each part.

Weeks 4 · 12 · 24

Monitoring

Scheduled reviews with a focused retest at twelve weeks, since HbA1c reflects roughly three months.

FAQ

Common questions

No. This is preventive and metabolic work that sits alongside your existing care. You get a written summary to share, and if something belongs with a specialist, you are referred.
Bring whatever you have, however old. Previous reports show direction of travel, and stop you paying for tests you have already done.
Only where a measured deficiency or specific clinical indication calls for it. Most gaps close with the plate. Nutrivance is a separate company and nothing is sold from this practice.
Energy and sleep often shift within weeks. Blood markers take longer — HbA1c reflects roughly three months, which is why the retest sits at twelve weeks.

Get In Touch

Tell me what brought you here.

Your message opens in WhatsApp, already written. You will get a reply with available slots and anything worth bringing along.

Clinic
Bhaskara Hospital
Gandimaisamma, Hyderabad, Telangana
Phone & WhatsApp
Languages
Telugu · English · Hindi · Urdu · Russian
Bring with you
Any reports from the last twelve months, and your current prescriptions
Urgent symptoms. Chest pain, breathlessness at rest, fainting or sudden weakness need emergency care now — not an appointment request.

Call the Clinic