Labcomp F
Labcomp F
Labcomp F
Venipuncture
Staff:
Certified Phlebotomist
Protocol:
Methods:
Blood is drawn from the examinee’s arm. In the laboratory the blood is processed, stored
and shipped to various laboratories for analysis. The complete blood count (CBC) results
are reported in the MEC and all other results are reported from NCHS to the participant.
Total Blood Draw 1-2 yrs 3-5 yrs 6-11yrs 12+ yrs
2007-08 9 ml 20 ml 33 ml 128 ml
2009-10 9 ml 20 ml 30 ml 117 ml
Time Allotment:
Depending on age of participant. Range 5-10 minutes.
Health Measures:
Laboratory test results.
Eligibility:
Sample persons aged 1 year and older who do not meet any of the exclusion criteria.
Exclusion Criteria:
Hemophiliacs
Participants who received chemotherapy within last 4 weeks
The presence of the following on both arms: rashes, gauze dressings, casts, edema,
paralysis, tubes, open sores or wounds, withered arms or limbs missing, damaged,
sclerosed or occluded veins, allergies to cleansing reagents, burned or scarred tissue,
shunt or IV.
Risks:
The following are known risks associated with venipuncture:
Hematoma
Swelling, tenderness and inflammation at the site
Persistent bleeding
Vasovagal response - dizziness, sweating, coldness of skin, numbness and tingling of
hands and feet, nausea, vomiting, possible visual disturbance, syncope and injury fall
from fainting.
Special precautions:
Sterile equipment issued with all sample persons.
Physician on call in case an adverse affect occurs.
Report of Findings:
The NHANES laboratory protocol assesses numerous environmental toxicants or their metabolites in
urine. Assessments of environmental exposures that are based on urine concentrations vary according
to the amount of urine produced. Currently, the NHANES urine measurements are adjusted by the
urinary creatinine concentration to account for variations in urinary dilution. However, creatinine
excretion into the urine varies by many factors other than the urinary dilution (e.g., age, gender, muscle
mass and diet). Also, the amount of toxicant that is excreted in a 24 hour period is usually required to
accurately quantify environmental exposures. Ideally, a 24 hour urine collection is performed, but this
is logistically impractical in NHANES. It is possible, however, to estimate the mass of analyte
excreted in the urine in a 24 hour period by estimating the urine flow for a casual urine specimen that
is collected as part of the current NHANES protocol.
Staff:
MEC Coordinator
Protocol:
Methods:
Urine is collected from participants aged 6 years and above. Survey participants will be asked to record
or recall the time of their last urine void prior to coming to the MEC.
Time Allotment:
2 minutes
Health Measures:
Laboratory test results.
Eligibility:
Sample persons aged 6 years and above.
Exclusion Criteria:
None
Special precautions:
None
Report of Findings:
Reported in the MEC: Pregnancy Test
Reported from NCHS: Other laboratory results
Bone mineral status markers
Laboratory Measures:
Vitamin D
Inclusion of serum 25(OH) D in NHANES will allow us to continue to assess vitamin D status in the
population. Interest in vitamin D status in the US has increased significantly in recent year. For
example, questions have been raised recently about the extent of vitamin D deficiency and
insufficiency in the U.S. population. Furthermore, the adequacy of the 1997 Dietary Reference Intake
recommendations for vitamin D in the U.S. are now being questioned, especially since new data
suggests that optimal serum 25(OH)D levels may be noticeably higher than previously thought.
Finally, recent studies have clarified that rickets still occurs in the U.S. Thus, it is important to include
these two measures of vitamin D status in the NHANES survey. In addition, this measure can be
linked with other measures included in the survey, such as blood pressure and bone mineral density, in
order to evaluate its role in both skeletal and nonskeletal conditions.
Vitamin D deficiency leads to a decrease in calcium absorption in the gastrointestinal tract and
overproduction of parathyroid hormone.
Diabetes Profile
Laboratory Measures:
Fasting Glucose, Insulin, Glycohemoglobin and Oral Glucose Tolerance Test
Diabetes is a large, growing, and costly public health problem in the United States and
disproportionately affects racial and ethnic minorities. About 17 million Americans have diabetes and
over 1 million new cases of diabetes are diagnosed each year. Diabetes is the leading cause of kidney
failure, non-traumatic lower extremity amputation, and blindness in working-age adults, and an
estimated $135 billion were spent on direct and indirect medical costs for diabetes in 2002.
Alarmingly, type 2 diabetes (formerly considered an adult disease) is now being diagnosed in children
and adolescents and there has been a large increase in diagnosed diabetes among adults <40 years of
age.
Information on the prevalence of diabetes disease, especially in its early stages, and associated risk
factors will be used to help develop early intervention and prevention programs for the disabling
consequences of this condition. Specifically, the diabetes disease examination will provide population
data to:
1. determine a national estimate of diabetes disease prevalence (diagnosed and undiagnosed),
including those at high risk for the late complications of the disease;
2. identify the risk factors of diabetes disease;
3. permit a national cohort to be established for follow-up studies of this condition; and
4. provide critical information to clinicians and public health officials for the development of
preventive care and community-based interventions.
In NHANES 2007, an oral glucose tolerance test continued in the survey to reassess the prevalence of
diabetes and IGT in the US population. Because of the increasing occurrence of diabetes in younger
ages, our collaborators, the National Institute of Diabetes, Digestive and Kidney Diseases and the
Division of Diabetes Translation at CDC have proposed that NHANES conduct the OGTT in
participants aged 12 and older.
Persons with impaired glucose tolerance (IGT) – 15.6% of the U.S. population – are at high risk for
developing diabetes. Also, IGT is an important risk factor for a number of other adverse health
conditions and mortality. IGT is defined on the basis of an abnormal oral glucose tolerance test
(OGTT). Persons without diabetes but with an OGTT 2-hr value of 140-199 mg/dL are considered to
have IGT. Recent national and international randomized controlled trials have shown that diabetes can
be delayed or prevented among persons with IGT. Furthermore, NHANES III data indicate a
tremendous opportunity for the prevention of diabetes - over 12 million persons aged 45-74 have pre-
diabetes (defined as overweight persons with either IGT or impaired fasting glucose metabolism).
These data also indicated that over 50% of persons with pre-diabetes are only detected by IGT
findings. As risk factors for diabetes, IGT, and pre-diabetes increase (e.g., physical inactivity, obesity,
and aging), consequently the prevalence of these conditions is also likely to increase.
The inclusion of OGTTs on NHANES will allow estimation of the prevalence of IGT and, thus, pre-
diabetes in the U.S. population, surveillance of trends in the prevalence and awareness of these
conditions, study of the risk factors for IGT and pre-diabetes, and examination of IGT as a risk factor
for health conditions and mortality. Timely data on IGT and pre-diabetes are particularly important as
the nation initiates efforts to prevent diabetes among persons with pre-diabetes. These data on IGT and
pre-diabetes are critical to targeting, designing, and evaluating prevention efforts, such as DHHS’s
STEPS program and efforts by the National Diabetes Education Program.
A fasting glucose blood test is performed on all participants 12 years and older who are examined in
the morning session after a 9-hour fast. After the venipuncture, participants are asked to drink 75
milligrams of Trutol® and to have a second venipuncture 2 hours (plus or minus 15 minutes) after the
first venipuncture.
Report of
Health Measure Eligibility Volume Required Findings Level
1 2 3
Glucose 12 and older 500uL
OGTT 12 and older 500uL
Insulin 12 and older 1 mL
Glycohemoglobin 12 and older 400 uL
Infectious Disease Profile
Laboratory Measures:
Hepatitis viruses
Among children aged 2-5 years anti-HBs (a maker of immunity) testing will be performed to assist in
the evaluation of the hepatitis B immunization program. If sufficient sera are available, other hepatitis
markers will be measured.
Hepatitis C (HCV) genotyping is the only change in the infectious disease assessment protocol. The
determination of HCV genotypes in NHANES will provide a nationally representative assessment of
genotype distribution of circulating HCV genotypes. Monitoring changes in this distribution over time
will provide insight into epidemiologic patterns of HCV infection in the U.S. In addition, the efficacy
of available treatments differs by genotype, and a snapshot of the nationwide distribution of HCV
genotypes may provide information on what the expected impact of treatment might be. Participants
ages 6 and older are eligible for Hepatitis C assessments.
Report of
Health Measure Eligibility Volume Required Findings Level
1 2 3
Hepatitis viruses 2-5 (anti-HBs), 400uL
6+ all other 1.5 ml
viruses
Oral Human Papilloma Virus
Infection with sexually transmitted human papillomavirus (HPV) is a cause of virtually all cervical
cancers. Molecular and epidemiological evidence also provides support for a role for HPV, particularly
HPV16, in the pathogenesis of a distinct subgroup of SCC of the head and neck. The relationship
between HPV and cervical cancer indicates that high-risk sexual behavior and exposure and infection
with HPV will increase the risk of other cancers caused by HPV. These associations have now been
consistently demonstrated for oropharyngeal cancers. Lifetime number of sexual partners as well as a
history of oral-genital and oral-anal sex have been independently associated with HPV-positive head
and neck cancers when compared with patients with HPV-negative cancers. In summary, current data
indicate that oral HPV16 infection is primarily sexually acquired and is a potential risk factor for
oropharyngeal cancer.
This proposal will provide estimates of the proportion of the U.S. population with oral HPV infection,
a probable risk factor for oral SCC. This data along with information concurrently collected in other
research studies on the natural history of oral HPV infection may provide additional information about
those at risk for HPV-positive oral SCC. This data will inform HPV prophylactic vaccine policy to
potentially prevent oral cancers.
Age Eligibility
Exclusion Criteria
None
The HPV oral rinse will be collected in the oral health examination room by the RDH. The oral health
examination will be conducted first. After that component is complete the RDH will collect the oral
rinse specimen.
Testing for 37 HPV types will be accomplished by means of a multiples polymerase-chain reaction
(PCR) assay. HPV-6, -11, -16, -18, -26, -31, -33, -35, -39, -40, -42, -45, -51, -52, -53, -54, -55, -56,
57, -58, -59, -61, -62, -64, -66, -67, -68, -69, -70, -71, -72, -73, -81, -82 (MM4 and IS39 subtypes), -83,
-84 and -89.
Report of findings
The results of the oral HPV tests will not be reported to participants. The state of knowledge for oral
HPV does not parallel that of vaginal HPV. Because we do report the vaginal results the following
contrasts the state of knowledge of vaginal and oral HPV to support the decision not to report the oral
HPV findings.
Although cervical cancer serves as a paradigm for HPV-mediated carcinogenesis in human subjects,
there are important distinctions between cervical cancer and oropharyngeal cancers. Much of the data
on the relationship between HPV and cervical cancer that have established the modern foundation for
cervical cancer screening do not apply to HPV-positive oropharyngeal cancers.
Miscellaneous Laboratory Assays
Laboratory Measures:
C-reactive protein, Thyroid Profile, and Standard Biochemical Profile includes Alanine
Aminotransferase (ALT), Albumin, Alkaline Phosphatase (ALP), Aspartate Aminotransferase (AST),
Bicarbonate (HCO3), Blood Urea Nitrogen (BUN), Calcium, Cholesterol, Creatinine, Gamma
Glutamyltransaminase (γ-GT), Glucose, Iron, Lactate Dehydrogenase (LDH), Phosphorus, Sodium,
Potassium, and Chloride, Total Bilirubin, Total Protein, Triglycerides, and Uric Acid.
Thyroid Profile
The thyroid profile contains thyroglobulin antibody, thyroxine (T3), thyroxine (T4), free,
thyroglobulin, thyroid stimulating hormone, thyroid peroxidase (TPO) antibody, thyroxine (T3), total,
and thryoxine (T4), total. Serum thyroid levels will be used to assess thyroid function and will provide
population-based reference information on these hormone levels. Thyroid function will be examined
in relation to measures of exposure to endocrine disrupting substances, which are hypothesized to
effect thyroid function (see laboratory protocol for environmental exposure assessments).
Low serum chloride values are associated with salt-losing nephritis; Addisonian
crisis, prolonged vomiting, and metabolic acidosis caused by excessive
production or diminished excretion of acids. High serum chloride values are
associated with dehydration and conditions causing decreased renal blood flow,
such as congestive heart failure.
p. T
otal Bilirubin
Elevated levels are associated with hemolytic jaundice, paroxysmal
hemoglobinuria, pernicious anemia, polycythemia, icterus neonatorum, internal
hemorrhage, acute hemolytic anemia, malaria, and septicemia. Low bilirubin
levels are associated with aplastic anemia, and certain types of secondary
anemia resulting from toxic therapy for carcinoma and chronic nephritis.
q. T
otal Protein
Total protein measurements are used in the diagnosis and treatment of a variety
of diseases involving the liver, kidney, or bone marrow, as well as other
metabolic or nutritional disorders.
r. T
riglycerides
Triglyceride measurements are used in the diagnosis of diabetes mellitus,
nephrosis, liver obstruction, and other diseases involving lipid metabolism and
various endocrine disorders and in the treatment of patients with these diseases.
s. Uric Acid
Uric acid measurements are used in the diagnosis and treatment of numerous
renal and metabolic disorders, including renal failure, gout, leukemia, psoriasis,
starvation or other wasting conditions and in the treatment of patients receiving
cytotoxic drugs.
Laboratory Measures:
Serum creatinine, blood urea nitrogen, urinary albumin and creatinine
Blood specimens will be used to obtain measures of serum creatinine and blood urea nitrogen. Urinary
albumin and creatinine will be measured. Self-reported information on chronic analgesic use and
incontinence will be collected.
The incidence of end stage kidney failure is increasing rapidly in the U.S. in adults of all age groups
which implies that the prevalence of progressive renal impairment is also increasing. However, little
information is known about the prevalence of chronic renal impairment on a national level. Urologic
disease, including urinary incontinence affects a large proportion of the population. Little nationally
representative data on the prevalence and risk factors associated with these conditions are available.
Report of Findings
Health Measure Eligibility Volume Required Level
1 2 3
Serum Creatinine/blood urea 12 and older 1 mL
nitrogen
Urinary albumin and 6 and older 3 mL
creatinine
Pregnancy Test and Prostate Specific Antigen (PSA)
Laboratory Measures:
Pregnancy test., PSA
b. PSA test
Prostate cancer is the most common non-skin malignancy among men with approximately 180,000
new cases diagnosed and 37,000 deaths in 1999. The total and free PSA tests have been recognized as
tumor markers for the screening, diagnosis and management of prostate cancer. The total PSA is not
specific for prostate cancer. Mildly elevated total PSA (above the cutoff of 4 ng/mL) can be seen in
benign prostatic hypertrophy and prostatitis. Falsely low PSA may be seen in men treated with
finasteride or taking herbals such as Saw Palmetto. The more recent free PSA assay is recommended
to increase the specificity when the total PSA is between 4-10 ng/mL. A percent free PSA (free/total
PSA X 100%) of less than 25% suggests prostate cancer
Additionally, in 2007 we will add complexed PSA (cPSA) to the PSA profile to establish national age
and race specific population reference values.
Report of Findings:
PSA: Male survey participants tested for PSA will receive test results in their Final Report of
Findings. If the result is greater than 4 ng/mL, an early reporting letter will be sent.
Pregnancy testing: Details and ethical considerations of reporting pregnancy test results are in
Attachment 30 – Pregnancy Testing.
Nutritional Biochemistries and Hematologies
Laboratory Measures:
Caffeine
Celiac disease
Serum ferritin
Serum vitamin B6
Complete blood counts, ferritin, transferrin receptor, vitamin B6, and vitamin D will continue in 2009.
Comparison study for the microbiological assay for RBC and serum folates subsamples will be cycled
out. Caffeine and celiac disease will be added in 2009.
Caffeine is a naturally occurring plant alkaloid primarily found in beverages such as coffee, tea, soft
drinks, and to a lesser extent in foods such as cocoa. Long recognized as a central nervous system
stimulant, caffeine is used both recreationally and medically as a means to combat drowsiness and
increase alertness. These effects are in large part responsible for the well-established widespread
consumption of traditional caffeinated beverages such as coffee, and the more recent “energy drinks”.
As a result, caffeine is believed to be the single-most widely consumed psychoactive substance in the
world. Epidemiologic studies of caffeine as a risk factor in major chronic diseases such as bladder
cancer, breast cancer, colon cancer, cardiovascular disease and various reproductive and perinatal
outcomes have yielded inconsistent results. Findings will not be reported to participants.
Celiac disease is an intolerance to dietary glutens that has protean manifestations. In population
surveys in other countries, it is found in about 0.5 to 1 percent of the population. It may well be as
common in the United States, but has not been adequately examined. Advances in diagnostic testing
now allow accurate disease prevalence estimates using two step serological testing--antihuman
recombinant - tissue transglutaminase (TTG) and endomysial antibody (EMA). An early report will be
sent to participants if both the TTG and EMA are positive.
Measurement of omega-3 fatty acids for participants 3 and older will be continued in the laboratory
component. In recent years, mounting scientific evidence has led to recommendations for increased
consumption of omega-3 fatty There are at least 10 ongoing NIH-funded studies testing the effects of
omega-3 fatty acids for conditions such as bipolar disorder, cancer, anorexia/cachexia, retinitis
pigmentosa, arrhythymias and stress. The reference data from NHANES will be useful for evaluation
of the concentrations achieved in these intervention studies.
Health Measures, Eligibility, Report of Findings:
Laboratory Measures:
Chlamydia trachomatis, Herpes simplex 1 and 2, HIV, Human papillomavirus virus (HPV) (antigen
from vaginal swabs, females age 14-59 years and HPV 16 antibody, all, age 14-59 years)
HSV-2 infections are rarely life threatening, but morbidity due to recurrent genital ulcerations is
substantial. Just as important, HSV-2 infection is the best current marker of sexual behavior risk
factors leading to sexually transmitted infections, generally, because: (a) HSV-2 infections are
common and, thus, HSV-2 rates are a sensitive measure of sexually transmitted infection risk factors;
(b) HSV-2 infection is almost always a result of sexual transmission and, thus, a specific measure of
sexually transmitted infection; (c) HSV-2 infections are not curable and, thus, HSV-2 risk is not
influenced by health care seeking factors; and (d) sensitive, specific, and relatively inexpensive tests
for HSV-2 antibody are available. HSV-2 is a very important index of the success of large national
efforts, motivated by the acquired immunodeficiency epidemic, to reduce risky sexual behaviors.
Human papillomavirus (HPV) (Vaginal s swab – DNA test; Blood test for antibody HPV
Genital human papillomavirus (HPV) infection is likely the most common sexually transmitted
infection in the U.S., and cervical infection with certain types of HPV, especially HPV-16, is the single
strongest risk factor for cervical cancer. No surveillance systems exist for HPV infections, the
majority of which are subclinical. Serum from participants aged 14-59 years will be tested for
antibody to HPV-16, the antigenic type most linked with cervical cancer to estimate the percentage of
individuals of both genders who have ever been infected with this virus. Testing of HPV DNA from
vaginal swabs from women 14-59 will provide an estimate of current infection. Vaginal swabs will be
tested for HPV DNA by the FDA approved Hybrid Capture II method (Digene) and by consensus PCR
with type specific analysis. The Hybrid Capture assay will detect overall high risk HPV types, but
cannot identify specific types. The PCR will allow identification of specific HPV type. Participants
will be notified of their Hybrid Capture results and specific messages will be developed to explain the
implications of the findings based on their age group.
Laboratory Measures:
Total Cholesterol, HDL- Cholesterol, LDL-Cholesterol, Triglycerides, and Apo B
1) Monitor the prevalence and trends in major cardiovascular conditions and risk factors in the U.S.;
2) Evaluate prevention and treatment programs targeting cardiovascular disease in the U.S.
The main element of the cardiovascular disease laboratory component in NHANES is blood lipid
levels. Cardiovascular disease is the leading cause of death in the United States. An estimated 4.8
million Americans have congestive heart failure. Increasing prevalence, hospitalizations, and deaths
have made congestive heart failure a major chronic condition in the United States.
One serum lipoprotein sub-fraction may emerge as independent risk factors for coronary heart disease
-Apolipoprotein B. The test was last measured in NHANES III in 1988-91 and 1991-94, respectively.
Serum, plasma and urine will continue to be stored for future research. Collection of a
genetic specimen will resume in 2007 after a four year hiatus
The availability of stored biologic specimens from a representative sample of the U.S.
population provides the scientific research community with a potential resource for the
measurement of new and evolving laboratory tests for emerging diseases, risk factors,
and environmental exposures. With the present explosion of gene determinations
associated with disease, the penetratence of susceptible genes in the population can only
be determined from a representative sample such as NHANES. The additional data
collected during the survey, both biochemical and questionnaire, provide phenotypic
information that can be associated with these genes.
NCHS will solicit proposals for use of the stored specimens. A technical panel will
review and approve all proposals. Proposals for performing genetic research will be
evaluated by the NHANES Genetic Technical Panel. All uses of stored specimens are
subject to review and approval by the NCHS Ethics Review Board and the NCHS
Confidentiality Officer.
All unused serum from laboratories will be stored for potential additional analyses.