Inborn errors of metabolism form a large class ofgenetic diseases involvingcongenital disorders of enzyme activities.[1] The majority are due to defects of singlegenes that code forenzymes that facilitate conversion of various substances (substrates) into others (products). In most of the disorders, problems arise due to accumulation of substances which are toxic or interfere with normal function, or due to the effects of reduced ability to synthesize essential compounds. Inborn errors of metabolism are often referred to ascongenital metabolic diseases orinherited metabolic disorders.[2] Another term used to describe these disorders is "enzymopathies". This term was created following the study ofbiodynamic enzymology, a science based on the study of the enzymes and their products. Finally,inborn errors of metabolism were studied for the first time by British physicianArchibald Garrod (1857–1936), in 1908. He is known for work that prefigured the"one gene–one enzyme" hypothesis, based on his studies on the nature and inheritance of alkaptonuria. His seminal text,Inborn Errors of Metabolism, was published in 1923.[3]
Traditionally the inherited metabolic diseases were classified as disorders ofcarbohydrate metabolism,amino acid metabolism,organic acid metabolism, orlysosomal storage diseases.[4] In recent decades, hundreds of new inherited disorders of metabolism have been discovered and the categories have proliferated. Following are some of the major classes of congenital metabolic diseases, with prominent examples of each class.[5]
Because of the enormous number of these diseases and the numerous systems negatively impacted, nearly every "presenting complaint" to a healthcare provider may have a congenital metabolic disease as a possible cause, especially in childhood and adolescence. The following are examples of potential manifestations affecting each of the major organ systems.[citation needed]
Dozens of congenital metabolic diseases are now detectable bynewborn screening tests, especially expanded testing using mass spectrometry.[6]Gas chromatography–mass spectrometry-based technology with an integrated analytics system has now made it possible to test a newborn for over 100 mm genetic metabolic disorders. Because of the multiplicity of conditions, many differentdiagnostic tests are used for screening. An abnormal result is often followed by a subsequent "definitive test" to confirm the suspected diagnosis.[citation needed]
Common screening tests used in the last sixty years:[citation needed]
Specific diagnostic tests (or focused screening for a small set of disorders):[citation needed]
A 2015 review reported that even with all these diagnostic tests, there are cases when "biochemical testing, gene sequencing, and enzymatic testing can neither confirm nor rule out an IEM, resulting in the need to rely on the patient's clinical course".[7] A 2021 review showed that several neurometabolic disorders converge on common neurochemical mechanisms that interfere with biological mechanisms also considered central inADHD pathophysiology and treatment. This highlights the importance of close collaboration between health services to avoidclinical overshadowing.[8]
In the middle of the 20th century the principal treatment for some of theamino acid disorders was restriction of dietary protein and all other care was simply management of complications. In the past twenty years, new medications, enzyme replacement, gene therapy, and organ transplantation have become available and beneficial for many previously untreatable disorders. Some of the more common or promising therapies are listed:[citation needed]
In a study inBritish Columbia, the overall incidence of the inborn errors of metabolism were estimated to be 40 per 100,000 live births or 1 in 2,500 births,[9] overall representing more than approximately 15% ofsingle gene disorders in the population.[9] While a Mexican study established an overall incidence of 3.4:1,000 live newborns and a carrier detection of 6.8:1,000 NBS.[10]
| Type of inborn error | Incidence | |
|---|---|---|
| Disease involving amino acids (e.g.PKU,Tyrosinemia), organic acids, primary lactic acidosis,galactosemia, or a urea cycle disease | 24 per 100,000 births[9] | 1 in 4,200[9] |
| Lysosomal storage disease | 8 per 100,000 births[9] | 1 in 12,500[9] |
| Peroxisomal disorder | ~3 to 4 per 100,000 of births[9] | ~1 in 30,000[9] |
| Respiratory chain-basedmitochondrial disease | ~3 per 100,000 births[9] | 1 in 33,000[9] |
| Glycogen storage disease | 2.3 per 100,000 births[9] | 1 in 43,000[9] |