Overlap syndrome

An overlap syndrome is a medical condition which shares features of at least two more widely recognised disorders. Examples of overlap syndromes can be found in many medical specialties such as overlapping connective tissue disorders in rheumatology, and overlapping genetic disorders in cardiology.

Overlap syndrome
SpecialtyRheumatology Edit this on Wikidata

Rheumatology

Examples of overlap syndromes in rheumatology include mixed connective tissue disease and scleromyositis. Diagnosis depends on which diseases the patient shows symptoms and has positive antibodies for in their lab serology.

In overlap syndrome, features of the following diseases are found (most common listed):[1]

The treatment of overlapping connective tissue disorders is mainly based on the use of corticosteroids and immunosuppressants. Biologic drugs, i.e. anti-TNFα or anti-CD20 monoclonal antibodies, have been recently introduced as alternative treatments in refractory cases. There are some concerns with the use of anti-TNF agents in patients with systemic autoimmune diseases due to the risk of triggering disease exacerbations.[2]

The term polyangiitis overlap syndrome refers to a systemic vasculitis that shares features with two or more distinct vasculitis syndromes. The most common type of polyangiitis overlap syndrome is microscopic polyangiitis (MPA), which shares features with EGPA, granulomatosis with polyangiitis and panarteritis nodosa. Sometimes polyangiitis overlap syndrome is used as a synonym for MPA.[3]

Gastroenterology

In gastroenterology, the term overlap syndrome may be used to describe autoimmune liver diseases that combine characteristic features of autoimmune hepatitis, primary biliary cirrhosis and primary sclerosing cholangitis.[4]

Cardiology

In cardiology, genetic conditions such as Brugada syndrome can share features with related disorders caused by mutations in the same gene. An overlap syndrome can be seen whereby a mutation in the SCN5A gene encoding the cardiac sodium channel causes a reduction in the peak sodium current leading to the typical ECG features of Brugada syndrome, but which simultaneously increases the sustained late sodium current leading to the ECG features of Long QT syndrome type 3.[5] Brugada syndrome can also overlap with arrhythmogenic cardiomyopathy due to certain mutations in the plakophilin gene.[6]

Pulmonology

In pulmonology, asthma-COPD Overlap Syndrome (ACOS) is a condition in which clinical features and symptoms of both asthma and COPD are present in a person and overlap significantly.[7]

See also

References
  1. Maddison PJ (December 1991). "Overlap syndromes and mixed connective tissue disease". Current Opinion in Rheumatology. 3 (6): 995–1000. doi:10.1097/00002281-199112000-00016. PMID 1772755. S2CID 43146562.
  2. Iaccarino L, Gatto M, Bettio S, Caso F, Rampudda M, Zen M, Ghirardello A, Punzi L, Doria A (January 2013). "Overlap connective tissue disease syndromes". Autoimmunity Reviews. 12 (3): 363–73. doi:10.1016/j.autrev.2012.06.004. PMID 22743033.
  3. Leavitt RY, Fauci AS (July 1986). "Polyangiitis overlap syndrome. Classification and prospective clinical experience". The American Journal of Medicine. 81 (1): 79–85. doi:10.1016/0002-9343(86)90186-5. PMID 2873744.
  4. Aguilar-Nájera O, Velasco-Zamora JA, Torre A (2015). "Overlap syndromes of autoimmune hepatitis: diagnosis and treatment". Revista de Gastroenterologia de Mexico. 80 (2): 150–9. doi:10.1016/j.rgmxen.2015.07.001. PMID 26091564.
  5. Wilde AA, Amin AS (May 2018). "Clinical Spectrum of SCN5A Mutations: Long QT Syndrome, Brugada Syndrome, and Cardiomyopathy". JACC: Clinical Electrophysiology. 4 (5): 569–579. doi:10.1016/j.jacep.2018.03.006. PMID 29798782.
  6. Cerrone M, Delmar M (July 2014). "Desmosomes and the sodium channel complex: implications for arrhythmogenic cardiomyopathy and Brugada syndrome". Trends in Cardiovascular Medicine. 24 (5): 184–90. doi:10.1016/j.tcm.2014.02.001. PMC 4099253. PMID 24656989.
  7. Postma, Dirkje S.; Rabe, Klaus F. (24 September 2015). "The Asthma–COPD Overlap Syndrome". New England Journal of Medicine. 373 (13): 1241–1249. doi:10.1056/NEJMra1411863. PMID 26398072.

Further reading
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