
Fingerstick
Amino Acids (Blood spot test)
Amino acids (Blood spot test)
€ 135,00
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Vitamins, minerals and amino acids · Blood
An amino acid that the body makes itself from glucose; needed for glycine and cell membranes, among other things.
At a glance
Explanation
Serine is an amino acid that the body can make itself from glucose and that is also found in protein-rich food. It is needed to make glycine, cysteine and substances in cell membranes and in the nervous system. This test measures serine in the blood.
Result
In adults without symptoms, a raised value of an amino acid is usually caused by a protein-rich meal or a protein shake shortly before the sample collection, by supplements containing amino acids (such as BCAAs, glutamine, arginine or taurine), or by the blood not being processed quickly enough. Reduced kidney function, liver disease, poorly controlled diabetes and some medicines can also raise values. A single, slightly raised value usually has no significance and causes no symptoms. Rarely, a strongly raised value, especially together with abnormalities in related amino acids, fits an inborn metabolic disease.
A low value is usually caused by fasting or a low-protein meal, or is a normal fluctuation. Eating little or little protein for a long time can lower the value. A low value does not mean you need serine as a supplement. Rarely, a markedly low value, preferably measured while fasting, fits an inborn disorder in the production of serine; this almost always already causes clear symptoms in childhood.
A slightly abnormal value in someone without symptoms usually does not lead to further tests; the GP looks at diet, supplements, medicines and the circumstances of the sample collection, and has the test repeated while fasting if needed. With strongly abnormal values or an abnormal pattern together with matching symptoms, the GP consults, or refers you to, an internist (specialist in internal medicine) or pediatrician with experience in metabolic diseases.
Reliability
In the Netherlands, amino acids are mainly measured in specialized laboratories for metabolic diseases, at the request of a specialist when an inborn metabolic disease is suspected or to monitor its treatment and diet. According to the American laboratory standard (ACMG), blood plasma, preferably collected while fasting, is the recommended sample; urine is less reliable as a first test, because the kidneys take back most amino acids and medicines can interfere with the measurement. As a 'functional' profile for finding deficiencies or tailoring supplements in adults without symptoms, the test has not been validated.
Who it is for
In hospitals, a specialist uses this test when a metabolic disorder is specifically suspected, or to monitor a known metabolic disease and the diet that goes with it. For adults without symptoms, to find nutritional deficiencies or to choose supplements, the test is not useful according to current knowledge. If you use protein supplements or single amino acids, you get a result that mainly shows that intake.
Inborn disorders of amino acid metabolism are rare. In the Netherlands, the heel prick finds on average about 12 children with PKU (phenylketonuria) per year and about 1 child with MSUD (maple syrup urine disease) or tyrosinemia type 1. There are no Dutch figures on abnormal amino acid values in adults without symptoms.
RIVM, heel prick screening (pns.nl)
Evidence
This explanation is based on Dutch guidelines and independent information. It is general information, not a diagnosis. Discuss an abnormal result with your GP.
More about risks and resultsMore explanations