Home Biomarkers Other compounds in Urine

Other compounds in Urine

Urine Analysis Biomarker

Sample Needed

Collection Type: Urine

Body System

Related System: Urine Analysis

Overview

"Other compounds in urine" refers to a group of non-routine or miscellaneous substances detected on a urinalysis beyond basic measurements (pH, specific gravity, protein, glucose). Commonly screened items include bilirubin, urobilinogen, nitrite, leukocyte esterase, ketones, blood/hemoglobin/myoglobin, and drug metabolites or unusual crystals. The test measures presence and approximate amount (often by dipstick or microscopic exam) to help detect liver disease, hemolysis, urinary tract infection, renal injury, metabolic derangements (ketoacidosis), rhabdomyolysis, or toxic exposures. Testing is prompted by jaundice, dark urine, abdominal pain, dysuria, frequency, fever, unexplained muscle pain, altered mental status, polyuria, or suspected poisoning. Results vary with age (neonates have physiologic bilirubin/urobilinogen patterns), sex (higher UTI risk in females), hydration, pregnancy, and renal concentrating ability.

Test Preparation

  • No special preparation is required

Why Do I Need This Test

  • Profile: included in a standard Urine Analysis (urinalysis) and may be part of targeted toxicology or metabolic panels.
  • Symptoms: jaundice, dark urine, dysuria, fever, flank pain, muscle weakness/pain, polyuria, confusion.
  • Diagnoses/monitor: liver disease, hemolysis, UTI, diabetic ketoacidosis, rhabdomyolysis, drug/toxin exposure.
  • Reasons for abnormal levels: liver obstruction or hepatocellular damage, hemolysis, bacterial infection, uncontrolled diabetes, muscle breakdown, recent drug use.
  • Biological meaning: abnormal findings point to organ dysfunction, infection, metabolic imbalance, or contamination.
  • Lifestyle/factors: diet, dehydration, medications, supplements, recent exercise, alcohol, and poor sample collection can alter results.
  • Family history: inherited metabolic liver or hemolytic disorders, kidney disease, or familial hyperlipidemia/toxic exposures may prompt testing.

Run our symptom checker to see if this test is right for you

Symptom Checker

Understanding Test Results

  • Bilirubin positive (any detectable bilirubin on dipstick) indicates conjugated hyperbilirubinemia think hepatocellular injury or biliary obstruction; requires liver function evaluation and imaging.
  • Urobilinogen >1.0 mg/dL (markedly >2 mg/dL) suggests increased bilirubin breakdown (hemolysis) or hepatocellular disease; absent or very low urobilinogen with positive bilirubin favors obstructive jaundice.
  • Nitrite positive indicates probable gram-negative bacterial UTI (eg, E.
  • coli).
  • A negative nitrite does not exclude UTI.
  • Leukocyte esterase trace/positive signals pyuria; together with nitrite or clinical symptoms strongly suggests UTI.
  • Any detectable urine glucose (glycosuria) is abnormal and suggests hyperglycemia exceeding renal threshold or proximal tubular dysfunction.
  • Ketones positive (trace to large) indicate ketosis/ketoacidosis from fasting, uncontrolled diabetes, or starvation; large amounts require urgent evaluation.
  • Dipstick positive for blood with RBCs on microscopy hematuria (stones, infection, glomerular disease, malignancy).
  • Dipstick positive but no RBCs myoglobinuria/hemoglobinuria (rhabdomyolysis or hemolysis) check CK and plasma hemoglobin.
  • Drug/toxin metabolites present indicate exposure and require correlation with history and confirmatory testing.
  • False positives/negatives can occur with concentrated or very dilute urine, certain medications, high vitamin C, improper collection, or interfering substances; abnormal findings typically prompt confirmatory microscopy, culture, blood testing, or imaging.

Normal Range

Bilirubin (urine): Negative Absent (0 mg/dL) Urobilinogen (urine): 0.2–1.0 mg/dL Nitrite (urine): Negative Absent Leukocyte esterase (urine): Negative Absent (0 leukocytes/µL) Glucose (urine): Negative Absent (≈0 mg/dL) Ketones (urine): Negative Absent (0 mg/dL) Blood (urine dipstick): Negative Absent (0 RBCs/HPF on microscopy) Drug metabolites (screen): Negative Absent Crystals/casts: None indicating pathology (occasional hyaline casts may be normal)

FAQs

Q: What are the compounds present in urine?

A: Normal human urine is about 95% water, the rest being solutes: mainly nitrogenous wastes such as urea, creatinine and uric acid; electrolytes (sodium, potassium, chloride, calcium, magnesium), ammonium and organic acids; small amounts of proteins, cells and pigments (urochrome), hormones and their metabolites, bilirubin, occasional glucose (pathologic), and excreted drugs and xenobiotic metabolites.

Q: What compound is found in urine?

A: Urea is the primary compound in human urine. It’s produced in the liver via the urea cycle to safely remove excess nitrogen from protein metabolism. Urine also contains creatinine, uric acid, electrolytes (sodium, potassium) and water. Urea concentration reflects hydration and kidney function; abnormal levels can indicate metabolic, renal, or dehydration issues.

Q: What are the abnormal compounds in urine?

A: Abnormal urine compounds include glucose (glycosuria), ketones, proteins (albumin), blood or hemoglobin, bilirubin and elevated urobilinogen, nitrites and leukocyte esterase (infection), casts and abnormal crystals, excess electrolytes, bacteria, drugs or toxins, and metabolic byproducts such as porphyrins. Their presence suggests diabetes, kidney or liver disease, infection or poisoning and requires further evaluation.

Q: What are the 13 components of urine?

A: Urine is mainly water (about 95%) plus metabolic wastes and dissolved electrolytes produced by kidney filtration and tubular processing. Thirteen common components are: water; urea; creatinine; uric acid; ammonium (ammonia); sodium; potassium; chloride; bicarbonate; calcium; phosphate; sulfate; and small amounts of protein (usually trace). Levels vary with diet, hydration and health.

Q: What are normal urine test results?

A: Normal urine is pale yellow, clear, with mild odor. pH about 4.5–8.0; specific gravity 1.005–1.030. No glucose, no/trace protein, no ketones, no bilirubin, no blood; nitrite and leukocyte esterase negative. Microscopy: few or no red/white blood cells (<5–10/HPF), few epithelial cells, no bacteria or significant crystals. Abnormal results may indicate infection, kidney disease, or metabolic issues.

Q: How do kidney infections develop?

A: Kidney infections (pyelonephritis) usually begin when bacteria—most commonly E. coli—enter the urinary tract, multiply in the bladder, and ascend the ureters to the kidneys. Risk factors include female anatomy, urinary retention, catheter use, kidney stones, vesicoureteral reflux, pregnancy, diabetes, or weakened immunity. Once bacteria reach renal tissue they cause inflammation, tissue damage and systemic symptoms needing prompt antibiotics.

Copyright 2020 © NirogGyan All rights reserved