All Inflammation Tests

Do you have chronic inflammation? 

Inflammation may be an indication of many diseases and illnesses. Ulta Lab Tests blood tests can detect chronic inflammation. 

One of the most prevalent indications of chronic illness is chronic inflammation. Inflammation may cause a slew of problems in the body, including changes in intestinal health, hormone balances, and more. Chronic inflammation can cause a wide range of health problems. Stopping the inflammatory process at its root requires a reduction in inflammation. You can identify inflammation and where it occurs in your body with inflammation blood tests. 

Click on the titles of the articles below to discover more about chronic inflammation and the lab tests that can help you.

You can order an inflammation blood test directly right now! Discover if you have a chronic inflammatory condition so you can obtain treatment before it can get worse. 

Ulta Lab Tests can help you take control of your health. We provide affordable lab tests online with 2,100 sites around the country, along with quick, convenient local testing and Quest Diagnostics results in as little as 24 to 48 hours for most tests. Ulta Lab Tests offers you the accurate test results you need to stay on track with your health. Furthermore, our affordable pricing is guaranteed, allowing you to receive the high-quality healthcare you deserve without breaking the bank. Ulta Lab Tests will enable you to test quickly and confidently. 

Take control of your health by ordering your blood tests to detect inflammation from the list below.


Name Matches

  • ANA Screen, IFA with Reflex to Titer and Pattern, IFA
  • Creatine Kinase (CK), Total
  • Homocysteine
  • hs-CRP
  • Sed Rate by Modified Westergren (ESR)
  • Uric Acid

Amylase
ANA Screen, IFA with Reflex to Titer and Pattern, IFA
Bilirubin, Direct
CBC (includes Differential and Platelets)
Comprehensive Metabolic Panel (CMP)
Creatine Kinase (CK), Total
Ferritin
Gamma Glutamyl Transferase (GGT)
Gliadin (Deamidated Peptide) Antibody (IgA)
Gliadin (Deamidated Peptide) Antibody (IgG)
Hemoglobin A1c (HgbA1C)
Homocysteine
hs-CRP
Immunofixation (IFE), Serum
Indican, Urine
Lactate Dehydrogenase (LD)
Lipase
Lipid Panel with Ratios
Omega-3 and -6 Fatty Acids, Plasma
Phosphate (as Phosphorus)
QuestAssureD™ 25-Hydroxyvitamin D (D2, D3), LC/MS/MS
Rheumatoid Factor
Thyroid Peroxidase Antibodies (TPO)
Uric Acid
Urinalysis (UA), Complete


  • ANA Screen, IFA with Reflex to Titer and Pattern, IFA
  • Creatine Kinase (CK), Total
  • Homocysteine
  • hs-CRP
  • Sed Rate by Modified Westergren (ESR)
  • Thyroid Peroxidase Antibodies (TPO)
  • Uric Acid

Ulta - Arthritis & Inflammation Deep Dive

This panel is a cure for WYSIATI – what-you-see-is-all-there-is. If all we do is measure a simple inflammation test, like the CRP, it is easy to fall into a trap of assuming inflammation is “arthritis”. But what if there is an infection or what if there is another reason for the pain or inflammation-like symptoms? Could it be a nutrient deficiency or excess? Could it be lack of recovery or abnormal stress hormone? This panel offers a remarkably deep dig into possible causes of inflammation, well beyond the typical tests ordered in practice. Sometimes our first impression is not the true answer. Results should be reviewed with you by a licensed healthcare provider.

  • ANA Screen, IFA with Reflex to Titer and Pattern, IFA #249
  • C-Reactive Protein (CRP) #4420
  • CBC (includes Differential and Platelets) #6399
  • Comprehensive Metabolic Panel (CMP) #10231
  • Cyclic Citrullinated Peptide (CCP) Antibody (IgG) #11173
  • Lipid Panel with Ratios #19543
  • Rheumatoid Factor #4418
  • Sed Rate by Modified Westergren (ESR) #809
  • Lyme Disease Antibodies (IgG, IgM), Immunoblot #8593
  • Cortisol, A.M. #4212
  • Creatine Kinase (CK), Total #374
  • DHEA Sulfate, Immunoassay #402
  • Ferritin #457
  • Hemoglobin A1c (HgbA1C) #496
  • Insulin #561
  • Testosterone, Free (Dialysis) and Total MS #36170
  • TSH #899
  • Vitamin B12 (Cobalamin) #927
  • Vitamin D, 25-Hydroxy, Total, Immunoassay #17306

DC - Comprehensive Inflammation Panel

OOL - Extensive Inflammation Panel

OOL - Extensive Inflammation Panel - without Sed Rate by Modified Westergren (ESR)


Clinical Significance

Rheumatoid Arthritis Diagnostic IdentRA® Panel 2 - Early diagnosis of rheumatoid arthritis (RA), ie, diagnosis before significant joint erosion occurs, is difficult. Psoriatic arthritis can also be difficult to diagnose clinically early in the disease process, and there are no specific biomarkers. The 14-3-3η (eta) protein is an emerging biomarker for RA and erosive psoriatic arthritis diagnosis. It may play a biologic role in the joint erosive process. Blood levels appear to be elevated in patients with RA, but not in other diseases including psoriasis, osteoporosis, gout, ulcerative colitis, type 1 diabetes, systemic lupus erythematosus, Crohn disease, primary Sjögren syndrome, scleroderma, and multiple sclerosis. The 14-3-3η protein, used in conjunction with rheumatoid factor (RF) and cyclic citrullinated peptide (CCP) antibody, may improve diagnostic sensitivity in the early diagnosis of RA. It may also help differentiate those with psoriatic arthritis joint damage from those without joint damage.


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Aids in the diagnosis of primary disease of skeletal muscle myocardial infarction and viral hepatitis.


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The major sources of amylase are the pancreas and the salivary glands. The most common cause of elevation of serum amylase is inflammation of the pancreas (pancreatitis). In acute pancreatitis, serum amylase begins to rise within 6-24 hours, remains elevated for a few days and returns to normal in 3-7 days. Other causes of elevated serum amylase are inflammation of salivary glands (mumps), biliary tract disease and bowel obstruction. Elevated serum amylase can also be seen with drugs (e.g., morphine) which constrict the pancreatic duct sphincter preventing excretion of amylase into the intestine.

Antinuclear antibodies are associated with rheumatic diseases including Systemic Lupus Erythematous (SLE), mixed connective tissue disease, Sjogren's syndrome, scleroderma, polymyositis, CREST syndrome, and neurologic SLE. 

Reflex Information: If ANA Screen, IFA is positive, then ANA Titer and Pattern will be performed at an additional charge.


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Measurement of the levels of bilirubin is used in the diagnosis and treatment of liver, hemolytic, hematologic, and metabolic disorders, including hepatitis and gall bladder obstruction. The assessment of direct bilirubin is helpful in the differentiation of hepatic disorders. The increase in total bilirubin associated with obstructive jaundice is primarily due to the direct (conjugated) fraction. Both direct and indirect bilirubin are increased in the serum with hepatitis.

Increased CRP levels are found in inflammatory conditions including: bacterial infection, rheumatic fever, active arthritis, myocardial infarction, malignancies and in the post-operative state. This test cannot detect the relatively small elevations of CRP that are associated with increased cardiovascular risk.


C-Reactive Protein Cardiac (hs CRP) Useful in predicting risk for cardiovascular disease.


C3a desArg is a cleavage product of C3 complement component activation. Elevated levels of C3a have been reported in patients with acute lyme disease, acute pancreatitis, systemic lupus erythematosus, and adult respiratory distress syndrome.


Clinical Significance

Used to diagnose inflammatory bowel disease (IBD), including Crohn's disease and ulcerative colitis, or to differentiate IBD from irritable bowel syndrome (IBS).

 

Collection Instructions

Collect undiluted feces in clean, dry sterile leak-proof container. Do not add fixative or preservative.

 


Low levels of fibrinogen are associated with bleeding most commonly secondary to liver disease or disseminated intravascular coagulation (DIC). Fibrinogen is an acute phase reactant and thus elevated levels may be associated with inflammation. Increased concentrations are also associated with increased risk of atherosclerosis.


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Chlamydia trachomatis RNA, TMA

Patient Preparation 

Urine specimens: The patient should not have urinated for at least one hour prior to specimen collection. Female patients should not cleanse the labial area prior to providing the specimen.

Urine: Patient should not have urinated within one hour prior to collection. Female patients should not cleanse the labial area prior to providing the specimen. Direct patient to provide a first-catch urine (a maximum of 20-30 mL of the initial urine stream) into a urine collection cup free of any preservatives. 2 mL of urine specimen must be transferred into the APTIMA® specimen transport within 24 hours of collection and before being assayed. Use tube provided in the urine specimen collection kit for urine specimens. The fluid (urine plus transport media) level in the urine tube must fall within the clear pane on the tube labe

Clinical Significance

C. trachomatis infections are the leading cause of sexually transmitted diseases in the united states. C. trachomatis is known to cause cervicitis, pelvic inflammatory disease (PID), epididymitis and proctitis. It is also the most frequent cause of non-gonococcal urethritis in men. Among women, the consequences of chlamydial infections are severe if left untreated. Approximately half of chlamydial infections are asymptomatic.


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Chlamydia/Neisseria gonorrhoeae RNA, TMA

Patient Preparation 

Urine specimen: The patient should not have urinated for at least one hour prior to specimen collection. Female patients should not cleanse the labial area prior to providing the specimen.

Urine: Patient should not have urinated within one hour prior to collection. Female patients should not cleanse the labial area prior to providing the specimen. Direct patient to provide a first-catch urine (a maximum of 20-30 mL of the initial urine stream) into a urine collection cup free of any preservatives. 2 mL of urine specimen must be transferred into the APTIMA® specimen transport within 24 hours of collection and before being assayed. Use tube provided in the urine specimen collection kit for urine specimens. The fluid (urine plus transport media) level in the urine tube must fall within the clear pane on the tube label.

 

Clinical Significance

C. trachomatis infections are the leading cause of sexually transmitted diseases in the United States. C. trachomatis is known to cause cervicitis, pelvic inflammatory disease (PID), epididymitis and proctitis. It is also the most frequent cause of non-gonococcal urethritis in men. Among women, the consequences of Chlamydialinfections are severe if left untreated. Approximately half of Chlamydial infections are asymptomatic.
Neisseria gonorrhoeae (gonococci) is the causative agent of gonorrhea. In men, this disease generally results in anterior urethritis accompanied by purulent exudate. In women, the disease is most often found in the cervix, but the vagina and uterus may also be infected.


A Complete Blood Count (CBC) Panel is used as a screening test for various disease states including anemia, leukemia, and inflammatory processes.

A CBC blood test includes the following biomarkers: WBC, RBC, Hemoglobin, Hematocrit, MCV, MCH, MCHC, RDW, Platelet count, Neutrophils, Lymphs, Monocytes, Eos, Basos, Neutrophils (Absolute), Lymphs (Absolute), Monocytes(Absolute), Eos (Absolute), Basos (Absolute), Immature Granulocytes, Immature Grans (Abs)

NOTE: Only measurable biomarkers will be reported.

Reflex Parameters for Manual Slide Review
  Less than  Greater Than 
WBC  1.5 x 10^3  30.0 x 10^3 
Hemoglobin  7.0 g/dL  19.0 g/dL 
Hematocrit  None  75%
Platelet  100 x 10^3  800 x 10^3 
MCV  70 fL  115 fL 
MCH  22 pg  37 pg 
MCHC  29 g/dL  36.5 g/dL 
RBC  None  8.00 x 10^6 
RDW  None  21.5
Relative Neutrophil %  1% or ABNC <500  None 
Relative Lymphocyte %  1% 70%
Relative Monocyte %  None  25%
Eosinophil  None  35%
Basophil  None  3.50%
     
Platelet  <75 with no flags,
>100 and <130 with platelet clump flag present,
>1000 
Instrument Flags Variant lymphs, blasts,
immature neutrophils,  nRBC’s, abnormal platelets,
giant platelets, potential interference
     
The automated differential averages 6000+ cells. If none of the above parameters are met, the results are released without manual review.
CBC Reflex Pathway

Step 1 - The slide review is performed by qualified Laboratory staff and includes:

  • Confirmation of differential percentages
  • WBC and platelet estimates, when needed
  • Full review of RBC morphology
  • Comments for toxic changes, RBC inclusions, abnormal lymphs, and other
  • significant findings
  • If the differential percentages agree with the automated counts and no abnormal cells are seen, the automated differential is reported with appropriate comments

Step 2 - The slide review is performed by qualified Laboratory staff and includes: If any of the following are seen on the slide review, Laboratory staff will perform a manual differential:

  • Immature, abnormal, or toxic cells
  • nRBC’s
  • Disagreement with automated differential
  • Atypical/abnormal RBC morphology
  • Any RBC inclusions

Step 3 If any of the following are seen on the manual differential, a Pathologist will review the slide:

  • WBC<1,500 with abnormal cells noted
  • Blasts/immature cells, hairy cell lymphs, or megakaryocytes
  • New abnormal lymphocytes or monocytes
  • Variant or atypical lymphs >15%
  • Blood parasites
  • RBC morphology with 3+ spherocytes, RBC inclusions, suspect Hgb-C,
  • crystals, Pappenheimer bodies or bizarre morphology
  • nRBC’s

Comprehensive Metabolic Panel