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Elecsys ACTH
07026684190 07026684500 100 cobas e 801
Short name ACN (application code number) M Streptavidin-coated microparticles, 1 bottle, 5.8 mL:
Streptavidin-coated microparticles 0.72 mg/mL; preservative.
ACTH 10075
R1 Anti-ACTH-Ab~biotin, 1 bottle, 7.2 mL:
Intended use Biotinylated monoclonal anti‑ACTH antibody (mouse) 0.3 mg/L;
Immunoassay for the in vitro quantitative determination of MESb) buffer 50 mmol/L, pH 6.2; preservative.
adrenocorticotropic hormone (ACTH) in human EDTA plasma.
The electrochemiluminescence immunoassay “ECLIA” is intended for use R2 Anti-ACTH-Ab~Ru(bpy) , 1 bottle, 7.2 mL:
on the cobas e 801 immunoassay analyzer. Monoclonal anti‑ACTH antibody (mouse) labeled with ruthenium
Summary complex 0.3 mg/L; MES buffer 50 mmol/L, pH 6.2; preservative.
Adrenocorticotropic hormone (ACTH) or corticotropin is a peptide hormone b) MES = 2-morpholino-ethane sulfonic acid
consisting of 39 amino acids. It is produced in the anterior pituitary of the Precautions and warnings
brain as part of the precursor molecule pro‑opiomelanocortin (POMC).
Tissue-specific cleavage results in ACTH and a range of related peptides.1,2 For in vitro diagnostic use.
Exercise the normal precautions required for handling all laboratory
ACTH stimulates formation and secretion of glucocorticoids (especially reagents.
cortisol) by the adrenal cortex. Disposal of all waste material should be in accordance with local guidelines.
The glucocorticoid production is regulated by various factors.3,4,5,6 After Safety data sheet available for professional user on request.
stimulation (e.g. by physical effort or by the internal body clock), the Avoid foam formation in all reagents and sample types (specimens,
hypothalamus secretes CRH (corticotropin releasing hormone). CRH acts calibrators and controls).
on the pituitary, which in turn synthesizes and secretes ACTH. Finally,
ACTH stimulates secretion of the glucocorticoids by the adrenals. High Reagent handling
concentrations of glucocorticoids in the blood inhibit secretion of CRH and The reagents in the kit have been assembled into a ready‑for‑use unit that
ACTH via a negative feedback mechanism. cannot be separated.
ACTH concentrations show a diurnal variation with high levels in the All information required for correct operation is available via the cobas link.
morning and low levels in the evening. Therefore, as with cortisol, it is
important to know the collection time of the plasma sample for interpretation Storage and stability
of the results. Store at 2‑8 °C.
Plasma ACTH measurements are useful in the differential diagnosis of Do not freeze.
Cushing's disease (ACTH hypersecretion), autonomous ACTH producing Store the cobas e pack upright in order to ensure complete availability of
pituitary tissue (e.g. Nelson's syndrome), hypopituitarism with ACTH the microparticles during automatic mixing prior to use.
deficiency and ectopic ACTH syndrome.7,8 In addition to cortisol
measurements, ACTH determinations can be used together with Stability:
suppression or stimulation tests to diagnose the origin of glucocorticoid
overproduction. Similarly, ACTH measurements can be employed to unopened at 2‑8 °C up to the stated expiration date
facilitate differential diagnosis of adrenocortical insufficiency (Addison’s on the cobas e 801 analyzer 16 weeks
disease).9
ACTH not produced by the pituitary gland is known as ectopic ACTH;10 this Specimen collection and preparation
is often associated with small cell carcinoma of the lung. In rare cases Only the specimens listed below were tested and found acceptable.
ectopic ACTH can be caused by thymic tumors, pancreatic K2‑EDTA and K3‑EDTA plasma, collected using siliconized glass tubes or
adenocarcinomas, or bronchial carcinoids. These tumors often secrete plastic tubes as ACTH adsorbs to non-siliconized glass tubes and thereby
ACTH precursors (POMC and pro‑ACTH). reduces sample ACTH values.2 Do not use other types of plasma samples.
The Elecsys ACTH assay employs two monoclonal antibodies specific for Criterion for K2‑EDTA plasma: Slope 0.85‑1.15 + coefficient of correlation
ACTH (9‑12) and for the C‑terminal region (ACTH 36‑39). ≥ 0.95 for method comparison vs K3‑EDTA plasma.
Due to common antigenic structure, the antibodies recognize intact Only use pre-cooled sampling vials. After drawing the blood, put the
biologically active ACTH 1‑39 and the ACTH precursors POMC and vials immediately on ice. Use a cooled centrifuge to separate the
pro‑ACTH.2 plasma. Measure samples immediately or freeze them at ‑20 °C.
Test principle Stable for 3 hours at 2‑8 °C followed by 2 hours at 20‑25 °C, 10 weeks at
Sandwich principle. Total duration of assay: 18 minutes. ‑20 °C (± 5 °C). Freeze only once.
The sample types listed were tested with a selection of sample collection
▪ 1st incubation: 30 µL of sample, a biotinylated monoclonal tubes that were commercially available at the time of testing, i.e. not all
ACTH‑specific antibody, and a monoclonal ACTH‑specific antibody available tubes of all manufacturers were tested. Sample collection systems
labeled with a ruthenium complexa) react to form a sandwich complex. from various manufacturers may contain differing materials which could
▪ 2nd incubation: After addition of streptavidin-coated microparticles, the affect the test results in some cases. When processing samples in primary
complex becomes bound to the solid phase via interaction of biotin and tubes (sample collection systems), follow the instructions of the tube
streptavidin. manufacturer.
▪ The reaction mixture is aspirated into the measuring cell where the Centrifuge samples containing precipitates before performing the assay.
microparticles are magnetically captured onto the surface of the Do not use heat‑inactivated samples.
electrode. Unbound substances are then removed with ProCell II M.
Application of a voltage to the electrode then induces chemiluminescent Do not use samples and controls stabilized with azide.
emission which is measured by a photomultiplier. Ensure the samples and calibrators are at 20‑25 °C prior to measurement.
▪ Results are determined via a calibration curve which is instrument- Due to possible evaporation effects, samples and calibrators on the
specifically generated by 2‑point calibration and a master curve provided analyzers should be analyzed/measured within 2 hours.
via the cobas link. Materials provided
a) Tris(2,2'-bipyridyl)ruthenium(II)-complex (Ru(bpy) ) See “Reagents – working solutions” section for reagents.
2018-10, V 2.0 English 1/4
07026684500V2.0
Elecsys ACTH
Materials required (but not provided) Conversion factors: pg/mL x 0.2202 = pmol/L
▪ 03255760190, ACTH CalSet, for 4 x 1.0 mL pmol/L x 4.541 = pg/mL
▪ 05341787190, PreciControl Multimarker, for 6 x 2.0 mL Limitations - interference
▪ General laboratory equipment The effect of the following endogenous substances and pharmaceutical
▪ cobas e 801 analyzer compounds on assay performance was tested. Interferences were tested
Accessories for the cobas e 801 analyzer: up to the listed concentrations and no impact on results was observed.
Elecsys ACTH
The plasma samples were drawn between 7‑10 a.m. Passing/Bablok11 Linear regression
ACTH concentrations vary considerably depending on physiological y = 1.07x - 0.412 y = 1.08x - 2.13
conditions. Therefore, ACTH results should always be evaluated together
with simultaneously measured cortisol concentrations. τ = 0.945 r = 1.00
Each laboratory should investigate the transferability of the expected values The sample concentrations were between 1.51 and 1702 pg/mL.
to its own patient population and if necessary determine its own reference
ranges. Analytical specificity
The Elecsys ACTH two‑site immunoassay measures intact ACTH 1‑39.
Specific performance data When ACTH fragments or peptides were added to a patient’s plasma
Representative performance data on the analyzer is given below. Results sample with defined ACTH concentration, no interference was observed
obtained in individual laboratories may differ. with ACTH 1‑10, ACTH 11‑24, beta‑MSH, beta‑Endorphin and POMC.
Precision ACTH fragments (ACTH 1‑17, ACTH 1‑24, ACTH CLIP 18‑39, ACTH 22‑39,
Precision was determined using Elecsys reagents, pooled human plasma alpha‑MSH 1‑13) can bind to one of the antibodies and thereby negatively
and controls in a protocol (EP05‑A3) of the CLSI (Clinical and Laboratory interfere with the sandwich formation and lead to lower ACTH values as
Standards Institute): 2 runs per day in duplicate each for 21 days (n = 84). shown in the following table:
The following results were obtained: Cross- Concentration Apparent Change in Cross-
cobas e 801 analyzer reactant of cross- ACTH ACTH reactivity
reactant pg/mL concentration %
Repeatability Intermediate
pg/mL pg/mL
precision
None; 0 55.4 not applicable not
Sample Mean SD CV SD CV
reference applicable
pg/mL pg/mL % pg/mL %
ACTH 1‑17 50000 16.9 -38.5 -0.077
Human plasma 1 2.73 0.115 4.2 0.176 6.4
5000 50.9 -4.5 -0.089
Human plasma 2 11.3 0.189 1.7 0.380 3.4
500 54.4 -1.0 -0.203
Human plasma 3 80.8 1.12 1.4 1.86 2.3
ACTH 1‑24 50000 10.1 -45.3 -0.091
Human plasma 4 753 11.7 1.5 18.5 2.5
5000 49.1 -6.3 -0.126
Human plasma 5 1828 28.9 1.6 42.8 2.3
500 55.3 -0.1 -0.022
PCc) Multimarker 1 38.8 1.16 3.0 1.71 4.4
ACTH 18‑39 50000 47.8 -7.6 -0.015
PC Multimarker 2 910 23.9 2.6 38.3 4.2
(CLIP) 5000 54.7 -0.7 -0.013
c) PC = PreciControl
500 55.8 0.4 0.075
cobas e 801 analyzer
ACTH 22‑39 50000 7.58 -47.8 -0.096
Repeatability Intermediate
5000 37.5 -17.9 -0.357
precision
500 52.9 -2.5 -0.491
Sample Mean SD CV SD CV
pmol/L pmol/L % pmol/L % ACTH 1‑13 50000 29.2 -26.2 -0.052
(alpha‑MSH) 5000 51.4 -4.0 -0.080
Human plasma 1 0.601 0.025 4.2 0.039 6.4
Human plasma 2 2.49 0.042 1.7 0.084 3.4 500 55.3 -0.1 -0.022
Human plasma 3 17.8 0.247 1.4 0.410 2.3 References
Human plasma 4 166 2.58 1.5 4.07 2.5 1 Cone RD. Anatomy and regulation of the central melanocortin system.
Nature Neurosci 2005;8:571-578.
Human plasma 5 403 6.36 1.6 9.42 2.3
2 Talbot JA, Kane JW, White A. Analytical and clinical aspects of
PC Multimarker 1 8.54 0.255 3.0 0.377 4.4 adrenocorticotrophin determination. Ann Clin Biochem
PC Multimarker 2 200 5.26 2.6 8.43 4.2 2003;40:453-471.
3 Jacobson L. Hypothalamic-pituitary-adrenocortical axis regulation.
Method comparison Endocrinol Metab Clin North Am 2005;34:271-292.
a) A comparison of the Elecsys ACTH assay, 03255751190 (y) with a 4 Arlt W, Stewart PM. Adrenal corticosteroid biosynthesis, metabolism,
commercially available ACTH test (x) using clinical samples gave the and action. Endocrinol Metab Clin North Am 2005;34:293-313.
following correlations (pg/mL):
5 Lin L, Achermann JC. The Adrenal. Horm Res 2004;62:22-29.
Number of samples measured: 180
6 Engelmann M, Landgraf R, Wotjak CT. The hypothalamic-
Passing/Bablok11 Linear regression neurohypophysial system regulates the hypothalamic-pituitary-adrenal
axis under stress: an old concept revisited. Front Neuroendocrinol
y = 1.08x + 1.23 y = 0.90x + 8.17 2004;25:132-149.
τ = 0.898 r = 0.992 7 Beauregard C, Dickstein G, Lacroix A. Classic and recent etiologies of
The sample concentrations were between 5.0 and 941 pg/mL (1.1 and Cushing’s syndrome: diagnosis and therapy. Treat Endocrinol
207 pmol/L). 2002;1:79-94.
b) A comparison of the Elecsys ACTH assay, 07026684190 8 Lindsay JR, Nieman LK. Differential diagnosis and imaging in
(cobas e 801 analyzer; y) with the Elecsys ACTH assay, Cushing’s syndrome. Endocrinol Metab Clin North Am
03255751190 (cobas e 601 analyzer; x) gave the following 2005;34:403-421.
correlations (pg/mL): 9 Napier C, Pearce SHS. Current and emerging therapies for Addison’s
Number of samples measured: 125 disease. Curr Opin Endocrinol Diabetes Obes 2014;21:147-153.
Elecsys ACTH
10 Oliver RL, Davis JR, White A. Characterization of ACTH related
peptides in ectopic Cushing’s syndrome. Pituitary 2003;6:119-126.
11 Bablok W, Passing H, Bender R, et al. A general regression procedure
for method transformation. Application of linear regression procedures
for method comparison studies in clinical chemistry, Part III.
J Clin Chem Clin Biochem 1988 Nov;26(11):783-790.
For further information, please refer to the appropriate operator’s manual for
the analyzer concerned, the respective application sheets, the product
information and the Method Sheets of all necessary components (if
available in your country).
A point (period/stop) is always used in this Method Sheet as the decimal
separator to mark the border between the integral and the fractional parts of
a decimal numeral. Separators for thousands are not used.
Symbols
Roche Diagnostics uses the following symbols and signs in addition to
those listed in the ISO 15223‑1 standard (for USA: see
https://usdiagnostics.roche.com for definition of symbols used):
Contents of kit
Analyzers/Instruments on which reagents can be used
Reagent
Calibrator
Volume after reconstitution or mixing
GTIN Global Trade Item Number
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