Characteristics of South Korean Patients with Hereditary Transthyretin Amyloidosis
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Background and Purpose This retrospective cross-sectional study included 18 patients from unrelated families harboring mutations of the transthyretin gene (TTR), and analyzed their characteristics and geographical distribution in South Korea. Methods The included patients had a diagnosis of systemic amyloidosis, clinical symptoms, such as amyloid neuropathy or cardiomyopathy, and confirmation of a TTR gene mutation using genetic analysis recorded between April 1995 and November 2014. Results The mean age at disease onset was 49.6 years, and the mean disease duration from symptom onset to diagnosis was 3.67 years. Fifteen of the 18 patients were classified as mixed phenotype, 2 as the neurological phenotype, and only 1 patient as the cardiac phenotype. The most-common mutation pattern in South Korea was Asp38Ala, which was detected in eight patients. Thirteen patients reported their family hometowns, and five of the eight harboring the Asp38Ala mutation were from the Gyeongsang province in southeast Korea. The other eight patients exhibited a widespread geographical distribution. A particularly noteworthy finding was that the valine at position 30 (Val30Met) mutation, which was previously reported as the most-common TTR mutation worldwide and also the most common in the Japanese population, was not detected in the present South Korean patients. Conclusions South Korean patients with hereditary TTR amyloidosis exhibited heterogeneous TTR genotypes and clinical phenotypes. The findings of this study suggest that the distribution of TTR amyloidosis in South Korea is due to de novo mutations and/or related to the other countries in East Asia.
Abstract
Background and Purpose This retrospective cross-sectional study included 18 patients from unrelated families harboring mutations of the transthyretin gene (TTR), and analyzed their characteristics and geographical distribution in South Korea. Methods The included patients had a diagnosis of systemic amyloidosis, clinical symptoms, such as amyloid neuropathy or cardiomyopathy, and confirmation of a TTR gene mutation using genetic analysis recorded between April 1995 and November 2014. Results The mean age at disease onset was 49.6 years, and the mean disease duration from symptom onset to diagnosis was 3.67 years. Fifteen of the 18 patients were classified as mixed phenotype, 2 as the neurological phenotype, and only 1 patient as the cardiac phenotype. The most-common mutation pattern in South Korea was Asp38Ala, which was detected in eight patients. Thirteen patients reported their family hometowns, and five of the eight harboring the Asp38Ala mutation were from the Gyeongsang province in southeast Korea. The other eight patients exhibited a widespread geographical distribution. A particularly noteworthy finding was that the valine at position 30 (Val30Met) mutation, which was previously reported as the most-common TTR mutation worldwide and also the most common in the Japanese population, was not detected in the present South Korean patients. Conclusions South Korean patients with hereditary TTR amyloidosis exhibited heterogeneous TTR genotypes and clinical phenotypes. The findings of this study suggest that the distribution of TTR amyloidosis in South Korea is due to de novo mutations and/or related to the other countries in East Asia.
참고문헌 (27)
- Saraiva MJ, "Transthyretin mutations in hyperthyroxinemia and amyloid diseases", Hum Mutat, 17, pp.493~503 (2001)
- Ikeda S, "Familial transthyretin-type amyloid polyneuropathy in Japan: clinical and genetic heterogeneity", Neurology, 58, pp.1001~1007 (2002)
- Sousa A, "Genetic epidemiology of familial amyloidotic polyneuropathy (FAP)-type I in Povoa do Varzim and Vila do Conde (north of Portugal)", Am J Med Genet, 60, pp.512~521 (1995)
- Holmgren G, "Diagnosis of familial amyloidotic polyneuropathy in Sweden by RFLP analysis", Clin Genet, 33, pp.176~180 (1988)
- Coelho T, "THAOS - The Transthyretin Amyloidosis Outcomes Survey: initial report on clinical manifestations in patients with hereditary and wild-type transthyretin amyloidosis", Curr Med Res Opin, 29, pp.63~76 (2013)
- Maurer MS, "Genotype and phenotype of transthyretin cardiac amyloidosis: THAOS (Transthyretin Amyloid Outcome Survey)", J Am Coll Cardiol, 68, pp.161~172 (2016)
- Kim HS, "An aggressive form of familial amyloid polyneuropathy caused by a Glu54Gly mutation in the transthyretin gene", Eur J Neurol, 12, pp.657~659 (2005)
- 김영진, "Transthyretin 유전자돌연변이를 보인 가족성 아밀로이드 다발신경병증", 대한신경과학회지, 29(3), pp.220~223 (2011), 대한신경과학회
- Ryu JK, "Familial amyloid polyneuropathy in Korea: the first case report with a proven ATTR Lys35Asn gene", Amyloid, 12, pp.62~64 (2005)
- Jang MA, "Asp58Ala is the predominant mutation of the TTR gene in Korean patients with hereditary transthyretin-related amyloidosis", Ann Hum Genet, 79, pp.99~107 (2015)
- Ando Y, "Guideline of transthyretin-related hereditary amyloidosis for clinicians", Orphanet J Rare Dis, 8, pp.31~ (2013)
- Nuvolone M, "Transthyretin-associated familial amyloid polyneuropathy-current and emerging therapies", US Neurology, 8, pp.24~32 (2012)
- Hsieh ST, "Amyloid neuropathy with transthyretin mutations: overview and unique Ala97Ser in Taiwan", Acta Neurol Taiwan, 20, pp.155~160 (2011)
- Yazak M, "Postmortem findings in two familial amyloidosis patients with transthyretin variant Asp38Ala", Amyloid, 7, pp.270~277 (2000)
- Reines JB, "Epidemiology of transthyretin-associated familial amyloid polyneuropathy in the Majorcan area: Son Llatzer Hospital descriptive study", Orphanet J Rare Dis, 9, pp.29~ (2014)
- Dardiotis E, "Epidemiological, clinical and genetic study of familial amyloidotic polyneuropathy in Cyprus", Amyloid, 16, pp.32~37 (2009)
- Kato-Motozaki Y, "Epidemiology of familial amyloid polyneuropathy in Japan: identification of a novel endemic focus", J Neurol Sci, 270, pp.133~140 (2008)
- TEX>, "<TEX>$GeneReviews^{(R)}$<", pp.2012, Sekijima Y
- Mascalchi M, "Transthyretin amyloidosis and superficial siderosis of the CNS", Neurology, 53, pp.1498~1503 (1999)
- Jones LA, "Proline at position 36: a new transthyretin mutation associated with familial amyloidotic polyneuropathy", Am J Hum Genet, 48, pp.979~982 (1991)
- Long D, "Vitreous amyloidosis in two large mainland Chinese kindreds resulting from transthyretin variant Lys35Thr and Leu55Arg", Ophthalmic Genet, 33, pp.28~33 (2012)
- Liu G, "Clinical features of familial amyloid polyneuropathy carrying transthyretin mutations in four Chinese kindreds", J Peripher Nerv Syst, 22, pp.19~26 (2017)
- Jacobson DR, "Variant-sequence transthyretin (isoleucine 122) in late-onset cardiac amyloidosis in black Americans", N Engl J Med, 336, pp.466~473 (1997)
- Swiecicki PL, "Hereditary ATTR amyloidosis: a single-institution experience with 266 patients", Amyloid, 22, pp.123~131 (2015)
- Takahashi K, "Familial amyloidotic polyneuropathy type 1 in Kumamoto, Japan: a clinicopathologic, histochemical, immunohistochemical, and ultrastructural study", Hum Pathol, 22, pp.519~527 (1991)
- Hattori T, "Clinical and pathological studies of cardiac amyloidosis in transthyretin type familial amyloid polyneuropathy", Amyloid, 10, pp.229~239 (2003)
- Yamashita T, "Genetic and clinical characteristics of hereditary transthyretin amyloidosis in endemic and non-endemic areas: experience from a single-referral center in Japan", J Neurol, 265, pp.134~140 (2018)