Dementia Blood Test Panel

Sodium (Na+) is an essential electrolyte measured primarily in blood serum or plasma. It plays a critical role in fluid balance, nerve impulse transmission, and muscle contraction. Serum sodium is one of the most commonly ordered laboratory tests, included in both the Basic and Comprehensive Metabolic Panels. Abnormal levels indicate conditions ranging from dehydration and kidney disease to hormonal imbalances. Sodium can also be measured in urine (to evaluate renal sodium handling) and stool (to differentiate causes of diarrhea).

Eosinophils are a type of white blood cell involved in allergic and parasitic responses. This test examines sputum (phlegm coughed up from lungs) under a microscope to detect eosinophils. Elevated sputum eosinophils suggest eosinophilic airway inflammation, which may indicate asthma, eosinophilic bronchitis, parasitic infections, or allergic conditions. This test helps diagnose conditions causing chronic cough and guides treatment selection.

This test measures glucose concentration in peritoneal dialysate fluid, the solution used during peritoneal dialysis for kidney failure. Glucose naturally diffuses from the dialysate into the bloodstream during treatment, and measuring residual glucose helps assess dialysate dwell time and treatment effectiveness. Changes in dialysate glucose levels can indicate peritoneal membrane changes or absorption problems affecting dialysis adequacy and treatment outcomes.

Chloride is an electrolyte essential for fluid balance, nerve signaling, and muscle function. This test measures chloride in peritoneal fluid (fluid around abdominal organs), which helps evaluate conditions affecting the abdomen such as peritonitis, ascites, or organ dysfunction. Abnormal chloride levels in peritoneal fluid can indicate infection, inflammation, or metabolic disturbances requiring medical attention.

Potassium is a vital electrolyte that regulates heart rhythm, muscle function, and fluid balance. Blood potassium testing is one of the most commonly ordered laboratory tests, included in both the Basic and Comprehensive Metabolic Panels. Hypokalemia (low potassium) can result from diuretic use, vomiting, or diarrhea and may cause muscle weakness, cramps, and dangerous cardiac arrhythmias. Hyperkalemia (high potassium) may result from kidney disease, certain medications (ACE inhibitors, potassium-sparing diuretics), or tissue damage. Both extremes require prompt clinical intervention due to life-threatening cardiac risks.

Globulins are proteins produced by the immune system and liver that function in immunity and nutrient transport. When measured in body fluids, globulin levels help assess immune function and protein status in specific body compartments. Elevated globulins in fluids like cerebrospinal or peritoneal fluid may indicate infection, inflammation, or immune-related conditions, while low levels could suggest nutritional deficiency or immune suppression.

Basophils are immune cells that release histamine and other chemicals during allergic reactions and inflammation. This test measures basophil counts in synovial fluid (joint fluid), which helps diagnose joint inflammatory conditions like rheumatoid arthritis, gout, or septic arthritis. Elevated basophils in joint fluid indicate inflammation or immune response in the joint. Results guide diagnosis and treatment of joint disease.

Carbon dioxide (CO2) in blood, measured as bicarbonate, is crucial for acid-base balance and respiration. This test assesses how well your lungs remove CO2 and how well your kidneys regulate acid balance. Elevated CO2 suggests respiratory problems or metabolic alkalosis, while low CO2 may indicate hyperventilation or metabolic acidosis. Results help diagnose breathing disorders, kidney disease, and serious metabolic imbalances affecting multiple organ systems.

Albumin is a protein produced by the liver and normally found in very small amounts in body fluids like urine. Microalbumin testing detects trace levels of albumin in urine that aren't visible on standard tests. The presence of albumin in urine—called albuminuria—is an early warning sign of kidney damage. This can result from diabetes, high blood pressure, or other kidney disease. Regular albumin screening helps detect kidney problems before significant damage occurs, allowing for early intervention and management to slow or prevent progression.

Creatinine is a waste product produced by muscle metabolism and filtered by the kidneys into urine. This test measures creatinine in an 8-hour urine collection and reflects kidney filtration function. Creatinine levels help assess kidney health and are often used to calculate glomerular filtration rate (GFR), which indicates how well your kidneys filter waste. Low creatinine output may suggest reduced muscle mass or kidney disease, while the ratio of protein to creatinine helps assess kidney protein loss. This test is frequently ordered in patients with diabetes, high blood pressure, or known kidney disease.

This test measures MTHFR, an enzyme critical for processing folate and producing molecules needed for DNA synthesis and methylation. MTHFR enzyme deficiency is a rare inherited metabolic disorder causing severe neurological problems, including intellectual disability, seizures, and movement disorders. Genetic variations (polymorphisms) in the MTHFR gene are common but usually don't cause disease. However, actual enzyme deficiency requires specialized treatment with folinic acid and other supplements. This test is ordered when genetic MTHFR deficiency is suspected based on neurological symptoms or family history.

Neutrophils are infection-fighting white blood cells. This test counts neutrophils in pleural fluid (fluid surrounding the lungs) to evaluate lung and pleural conditions. Elevated neutrophils in pleural fluid suggest infection, inflammation, or malignancy affecting the lungs or pleural lining. The test also notes that elevated neutrophils in prostatic secretions may indicate prostate inflammation or prostatitis. Analysis of pleural fluid composition, including neutrophil count, helps diagnose pneumonia with effusion, empyema (infected fluid), or other serious lung conditions requiring urgent treatment.

Bilirubin is a yellowish compound produced when your body breaks down old red blood cells. When measured in pericardial fluid (fluid around the heart), elevated bilirubin can indicate liver disease, hemolysis (breakdown of red blood cells), or bile duct obstruction. It can also reflect pericardial inflammation or infection. This specialized test helps diagnose serious cardiac and metabolic conditions affecting the tissue surrounding your heart.

White blood cells (WBCs or leukocytes) are immune cells that fight infections and protect your body. This test measures WBC count in synovial fluid (fluid surrounding joints). Elevated WBC in joint fluid suggests infection, inflammation, or autoimmune disease affecting that joint. Very high counts may indicate septic arthritis (bacterial infection), while moderate elevation could indicate rheumatoid arthritis or other inflammatory joint conditions. This specialized test helps diagnose the cause of joint pain or swelling.

Platelets are small blood cells essential for blood clotting and preventing excessive bleeding. This blood test counts the number of platelets circulating in your bloodstream. Low platelet counts (thrombocytopenia) increase bleeding risk, while high counts (thrombocytosis) may indicate clotting risks or underlying disease. Platelet counts are affected by bone marrow disorders, medications, infections, and autoimmune diseases. This is a routine test included in complete blood counts to assess clotting function and overall blood health.

Monocytes are large white blood cells that help fight infections and clear damaged tissue. This specialized test counts monocytes in pericardial fluid (fluid around the heart). Elevated monocyte counts in pericardial fluid may indicate pericarditis (inflammation of the heart lining), infection, or autoimmune disease affecting the heart. This test helps diagnose serious cardiac conditions and inflammatory states. Results are interpreted alongside other fluid analysis tests for comprehensive cardiac assessment.

Red blood cells (erythrocytes) are the oxygen-carrying cells in your blood. This automated test counts the number of red blood cells in synovial fluid (joint fluid), which is abnormal since red blood cells should not be present in joints. Elevated RBC counts in joint fluid may indicate joint injury, bleeding into the joint, or traumatic arthrocentesis (needle puncture during fluid collection). This result helps differentiate between inflammatory and non-inflammatory joint conditions.

Calcium is an essential mineral critical for bone health, muscle function, nerve signaling, and blood clotting. This test measures calcium levels in serum or plasma, reflecting overall calcium balance in the body. About 99% of calcium is stored in bones, while the remaining 1% circulates in the blood and is tightly regulated. Abnormal serum calcium may indicate parathyroid disorders, vitamin D deficiency, kidney disease, or certain malignancies. Both hypocalcemia (low calcium) and hypercalcemia (high calcium) can cause serious symptoms including muscle cramps, cardiac arrhythmias, and neurological changes.

Alkaline phosphatase (ALP) is an enzyme found in bones, liver, and intestines. It plays a role in bone formation and bile production. This test measures ALP levels to assess bone metabolism and liver function. Elevated ALP can indicate bone disease (osteoporosis, fractures, or Paget's disease), liver disease, or bile duct obstruction. Low levels are less common but may suggest nutritional deficiencies or genetic conditions. ALP is often part of routine health screening or organ function assessment.

Urea nitrogen in urine reflects protein metabolism and kidney function. This test, typically performed on 12-hour or 24-hour urine collections, measures how much nitrogen from protein breakdown is excreted daily. Abnormal levels can indicate dietary protein intake changes, kidney disease, liver dysfunction, or metabolic disorders. The test helps assess protein metabolism, evaluate kidney function, and monitor nutritional status in patients with various metabolic or renal conditions.

Aspartate aminotransferase (AST) is an enzyme found primarily in liver and muscle cells. When cells are damaged, AST leaks into the bloodstream where it can be measured. Elevated AST suggests liver damage from hepatitis, cirrhosis, fatty liver disease, or alcohol use, but can also reflect muscle injury from trauma, intense exercise, or heart attack. AST is typically ordered alongside other liver enzymes (ALT, alkaline phosphatase) to assess liver function. Moderate elevations may be temporary and benign, but persistent elevation requires investigation to identify the underlying cause.

Mean sphered cell volume measures the average size of red blood cells when treated under standardized laboratory conditions. This specialized test provides information about red blood cell shape and hydration status, helping diagnose hemolytic anemias and hereditary conditions affecting RBC structure like spherocytosis. Abnormal values suggest specific types of anemia or blood disorders requiring further investigation and targeted treatment.

Hemoglobin is the iron-containing protein in red blood cells that carries oxygen throughout your body. A hemoglobin test measures the total amount of hemoglobin in blood, revealing whether you have anemia (too little) or polycythemia (too much). Low hemoglobin causes fatigue, shortness of breath, and weakness, while high levels can increase clot risk. This is one of the most common tests in clinical medicine and a core part of the complete blood count.

Alanine aminotransferase (ALT) is an enzyme found primarily in liver cells that leaks into the bloodstream when liver tissue is damaged or inflamed. This blood test measures ALT levels to assess liver health and detect conditions like hepatitis, fatty liver disease, cirrhosis, or medication-related liver injury. Elevated ALT typically indicates liver damage or disease, while normal levels suggest the liver is functioning properly. ALT is often part of routine health screening and is essential for monitoring patients taking medications known to affect the liver.

This test identifies specific mutations in the EGFR (epidermal growth factor receptor) gene from blood or tissue samples. EGFR mutations are commonly found in certain lung cancers and can determine which targeted therapies will be most effective. Different mutations respond differently to specific medications called EGFR inhibitors. Testing for EGFR mutations is crucial for cancer patients to guide treatment selection, predict drug response, and optimize outcomes. This genetic information helps oncologists personalize cancer treatment plans.

This urine test measures the ratio of albumin to globulin proteins. Albumin is normally filtered minimally by healthy kidneys, while globulin appears in urine in very small amounts. An elevated albumin-to-globulin ratio in urine may indicate early kidney damage or diabetes-related kidney disease. Proteinuria (excess urinary protein) is an early warning sign of kidney dysfunction and cardiovascular risk. Monitoring this ratio helps track kidney health and response to treatment for diabetes or hypertension.

The erythrocyte sedimentation rate (ESR) measures how quickly red blood cells settle in a test tube over one hour. This simple test reflects inflammation levels in your body. Elevated ESR can indicate infections, autoimmune diseases, inflammatory conditions, or certain cancers. Low ESR is less common but may occur with blood disorders. ESR is often used alongside other tests to diagnose or monitor chronic inflammatory conditions, though it's not specific to any single disease.

Nucleated red blood cells (nRBCs) are immature RBCs that normally exit the bone marrow and mature before circulating in your blood. The presence of nucleated RBCs in peripheral blood is abnormal and suggests bone marrow stress or disease. This can indicate severe anemia, leukemia, infection, hemolysis, or other serious conditions. Finding nucleated RBCs on a blood smear typically warrants further investigation to identify the underlying cause.

Thyroid stimulating hormone (TSH) is produced by the pituitary gland and regulates thyroid hormone production. A TSH test is the primary screening tool for thyroid disorders. Elevated TSH suggests an underactive thyroid (hypothyroidism), while low TSH may indicate an overactive thyroid (hyperthyroidism). Thyroid function affects metabolism, energy, weight, and mood. This is one of the most frequently ordered tests because thyroid dysfunction is common and affects overall health.

Band form neutrophils (bands) are immature white blood cells released from the bone marrow into the bloodstream in response to acute infection or inflammation. An elevated band count, known as a "left shift," is a hallmark of bacterial infection and sepsis. Bands are counted as part of the manual differential on a complete blood count (CBC). Their presence signals the body's urgent demand for neutrophils and is one of the SIRS criteria used in critical care. Monitoring band counts helps track infection severity and response to antibiotic therapy.

Lymphocytes are a type of white blood cell crucial for the adaptive immune response, including B cells (which produce antibodies), T cells (which coordinate and carry out cell-mediated immunity), and NK cells (natural killer cells). This blood test counts lymphocytes as part of the complete blood count with differential. Elevated lymphocyte counts (lymphocytosis) may suggest viral infections, certain leukemias, or autoimmune conditions. Low lymphocyte counts (lymphopenia) can indicate immunodeficiency, bone marrow disorders, or the effects of immunosuppressive therapies.

Myelocytes are immature white blood cells normally found in bone marrow. Their presence in body fluids such as blood, pleural fluid, or peritoneal fluid is abnormal and may indicate serious conditions. Myelocytes in body fluids can suggest leukemia, severe infection, or other hematologic disorders. The number and type of myelocytes detected helps establish a diagnosis. This test is typically ordered when other findings suggest a blood cell disorder and requires interpretation alongside other cell counts and clinical findings.

Folate is a B vitamin essential for DNA synthesis, cell division, and red blood cell formation. Your body cannot make folate, so it must come from foods like leafy greens, legumes, and fortified grains. Low folate levels can cause anemia, fatigue, and neurological problems. During pregnancy, adequate folate is critical for fetal development. High folate levels are rare but may suggest certain health conditions. This test screens for deficiency, which is common in vegetarians, people with malabsorption disorders, and those taking certain medications.

EGFR (epidermal growth factor receptor) is a gene that, when mutated, can drive certain lung cancers and other malignancies. This test analyzes blood or tissue samples for specific EGFR mutations. Detecting these mutations is critical for patients with non-small cell lung cancer because it determines eligibility for targeted therapy drugs (like erlotinib or gefitinib) that specifically block the mutated EGFR protein. These targeted treatments are often more effective and better tolerated than traditional chemotherapy. This is a molecular diagnostic test that informs personalized cancer treatment strategies.

Blasts are immature blood or bone marrow cells. Finding them in body fluids (blood, joint fluid, pleural fluid, etc.) is abnormal and concerning. In healthy individuals, blasts should not appear in body fluids—they should remain in bone marrow and blood. Their presence may indicate leukemia, other blood cancers, or malignant invasion into body cavities. This is a quantitative test that counts the number of blasts, which helps assess disease severity. Further testing and specialist evaluation are essential if blasts are detected.

Promyelocytes are immature white blood cells normally found in bone marrow, not in body fluids like blood or joint fluid. Detecting promyelocytes in body fluids is abnormal and may indicate serious conditions such as leukemia, particularly acute promyelocytic leukemia (APL), or leukostasis. The presence and quantity of promyelocytes helps diagnose blood cancers and assess disease severity. This finding requires urgent further investigation and specialist consultation.

Metamyelocytes are immature white blood cells found in bone marrow that normally do not appear in significant numbers in body fluids. Their presence in blood, joint fluid, or other body compartments is abnormal and may indicate leukemia, severe infection, or a bone marrow disorder. This test counts metamyelocytes as part of a differential analysis in body fluid samples. Elevated levels suggest the bone marrow is releasing immature cells prematurely, which warrants further investigation.

CLSI (formerly NCCLS) document "Reference Leukocyte Differential Count (Proportional) and Evaluation of Instrumental Methods", 1992, recommend the use of variant lymphocytes rather than atypical or reactive lymphocytes.

1,25-dihydroxyvitamin D2 is the active, hormonally potent form of vitamin D derived from plant and fungal sources (ergocalciferol). A 1,25-D2 test measures this specific form, which is biologically active at very low concentrations. Elevated levels may indicate excessive supplementation, granulomatous diseases (like sarcoidosis), or lymphomas that abnormally produce this hormone. This test is more specialized than standard vitamin D testing and is useful for investigating specific clinical conditions.

1,25-dihydroxyvitamin D is the most biologically active form of vitamin D, produced primarily by the kidneys. This test measures circulating levels of active vitamin D in your blood. Vitamin D is essential for calcium absorption, bone health, immune function, and mood regulation. Low levels may indicate kidney disease, vitamin D deficiency, or calcium disorders, while abnormally high levels can occur with excessive supplementation or certain granulomatous diseases. This test is particularly useful for evaluating bone health and metabolic disorders.

CD19 is a marker found on B lymphocytes, white blood cells that produce antibodies and fight infections. A CD19 cell count measures the number of B cells in your blood or bone marrow. Abnormally low CD19 counts may indicate immunodeficiency, leukemia, or complications from certain medications or treatments. Elevated counts can suggest chronic lymphocytic leukemia or other lymphoproliferative disorders. This test is particularly useful in diagnosing blood cancers and immune disorders.

This category encompasses laboratory test results that have been sent to a specialized reference laboratory for advanced or specialized testing. Reference labs perform complex analyses that are not available at routine hospital or clinic labs, such as genetic testing, specialized microbiology cultures, or complex immunological assays. Results from these tests provide detailed diagnostic information for uncommon or complicated medical conditions.

Band neutrophils are immature white blood cells released from bone marrow during stress or infection. This test measures the percentage of band neutrophils relative to total white blood cells. Elevated bands (a left shift) typically indicate acute infection, inflammation, or leukemia. Normal blood contains mostly mature segmented neutrophils; a high proportion of bands suggests the bone marrow is urgently releasing immature cells to fight infection.

This comprehensive vitamin D panel measures three forms: 25-hydroxyvitamin D (the storage form that indicates overall status), vitamin D2 (from dietary sources), and 1,25-dihydroxyvitamin D3 (the active form). Together, these tests assess vitamin D metabolism and availability. Vitamin D is essential for calcium absorption, bone health, immune function, and mood. Deficiency is linked to weak bones, increased infection risk, and depression.

This test calculates the ratio of blood urea nitrogen (BUN) to creatinine, both waste products filtered by the kidneys. The ratio helps distinguish different causes of abnormal kidney function. A high ratio may suggest dehydration, excessive protein breakdown, or reduced kidney blood flow, while a low ratio can indicate liver disease or malnutrition. This ratio is more informative than either value alone in determining kidney dysfunction patterns.

This test measures total 25-hydroxyvitamin D, combining both vitamin D2 (from foods and supplements) and vitamin D3 (from sun exposure and food). The 25-hydroxy form is the best indicator of overall vitamin D status because it reflects total body stores. This single measurement efficiently assesses vitamin D adequacy for bone health, immune function, and calcium regulation without measuring multiple vitamin D forms.

Cobalamin, also known as vitamin B12, is an essential nutrient required for nerve function, red blood cell formation, and DNA synthesis. This test measures B12 levels in blood. Deficiency causes pernicious anemia, nerve damage, and cognitive problems. B12 deficiency is common in vegetarians, older adults, and people with gastrointestinal disorders. Low levels require supplementation through injections or high-dose oral supplements to restore normal function.

GFR measures how efficiently your kidneys filter waste from blood, expressed as milliliters of filtrate per minute. It's calculated using creatinine levels adjusted for age, sex, and body size. GFR is the most accurate indicator of kidney function, with different stages indicating mild, moderate, or severe kidney disease. Even small declines in GFR can signal progressive kidney disease requiring monitoring and lifestyle modifications to slow progression.

Platelets are cell fragments essential for blood clotting and stopping bleeding. This test counts platelets in blood, with the Rees-Ecker method being a manual counting technique. Normal platelet counts range from 150,000 to 400,000 per microliter. Low platelet counts (thrombocytopenia) increase bleeding risk, while high counts (thrombocytosis) increase clot risk. Abnormal counts may indicate bone marrow disorders, autoimmune disease, infections, or medication effects.