Increased risk of sudden death in untreated primary carnitine deficiency
Primary carnitine deficiency (PCD) affects fatty acid oxidation and is associated with cardiomyopathy and cardiac arrhythmia, but the risk of sudden death in PCD is unknown. The Faroe Islands have a high prevalence of PCD, 1:300. This study systematically investigated a possible association between...
Saved in:
Published in | Journal of inherited metabolic disease Vol. 43; no. 2; pp. 290 - 296 |
---|---|
Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken, USA
John Wiley & Sons, Inc
01.03.2020
Blackwell Publishing Ltd |
Subjects | |
Online Access | Get full text |
ISSN | 0141-8955 1573-2665 1573-2665 |
DOI | 10.1002/jimd.12158 |
Cover
Abstract | Primary carnitine deficiency (PCD) affects fatty acid oxidation and is associated with cardiomyopathy and cardiac arrhythmia, but the risk of sudden death in PCD is unknown. The Faroe Islands have a high prevalence of PCD, 1:300. This study systematically investigated a possible association between untreated PCD and sudden death in young Faroese subjects. We investigated all medico‐legal cases of sudden death between 1979 and 2012 among subjects below the age of 45. Stored biomaterial was examined with molecular genetic analysis to reveal PCD. We compared the prevalence of PCD among sudden death cases with that of the background population (0.23%) to calculate the odds ratio (OR) for sudden death with PCD. Biomaterial was available and genetically analyzed from 53 of 65 sudden death cases (82%) in the Faroe Islands. Six (one male and five females) of the 53 cases were homozygous for the PCD related c.95A>G mutation—a prevalence of 11.3% (95% CI 5%‐23%) and an OR of 54.3 (95% CI 21‐138, P < .0001) for the association between sudden death and untreated PCD. Only 11 of the 53 sudden death cases were women—of whom five were homozygous for the c.95A>G mutation (45.5%) yielding an OR of 348.8 (95% CI 94‐1287, P < .0001) for the association between sudden death and untreated PCD in females. This study showed a strong association between sudden death and untreated PCD, especially in females. |
---|---|
AbstractList | Primary carnitine deficiency (PCD) affects fatty acid oxidation and is associated with cardiomyopathy and cardiac arrhythmia, but the risk of sudden death in PCD is unknown. The Faroe Islands have a high prevalence of PCD, 1:300. This study systematically investigated a possible association between untreated PCD and sudden death in young Faroese subjects. We investigated all medico-legal cases of sudden death between 1979 and 2012 among subjects below the age of 45. Stored biomaterial was examined with molecular genetic analysis to reveal PCD. We compared the prevalence of PCD among sudden death cases with that of the background population (0.23%) to calculate the odds ratio (OR) for sudden death with PCD. Biomaterial was available and genetically analyzed from 53 of 65 sudden death cases (82%) in the Faroe Islands. Six (one male and five females) of the 53 cases were homozygous for the PCD related c.95A>G mutation-a prevalence of 11.3% (95% CI 5%-23%) and an OR of 54.3 (95% CI 21-138, P < .0001) for the association between sudden death and untreated PCD. Only 11 of the 53 sudden death cases were women-of whom five were homozygous for the c.95A>G mutation (45.5%) yielding an OR of 348.8 (95% CI 94-1287, P < .0001) for the association between sudden death and untreated PCD in females. This study showed a strong association between sudden death and untreated PCD, especially in females. Primary carnitine deficiency (PCD) affects fatty acid oxidation and is associated with cardiomyopathy and cardiac arrhythmia, but the risk of sudden death in PCD is unknown. The Faroe Islands have a high prevalence of PCD, 1:300. This study systematically investigated a possible association between untreated PCD and sudden death in young Faroese subjects. We investigated all medico‐legal cases of sudden death between 1979 and 2012 among subjects below the age of 45. Stored biomaterial was examined with molecular genetic analysis to reveal PCD. We compared the prevalence of PCD among sudden death cases with that of the background population (0.23%) to calculate the odds ratio (OR) for sudden death with PCD. Biomaterial was available and genetically analyzed from 53 of 65 sudden death cases (82%) in the Faroe Islands. Six (one male and five females) of the 53 cases were homozygous for the PCD related c.95A>G mutation—a prevalence of 11.3% (95% CI 5%‐23%) and an OR of 54.3 (95% CI 21‐138, P < .0001) for the association between sudden death and untreated PCD. Only 11 of the 53 sudden death cases were women—of whom five were homozygous for the c.95A>G mutation (45.5%) yielding an OR of 348.8 (95% CI 94‐1287, P < .0001) for the association between sudden death and untreated PCD in females. This study showed a strong association between sudden death and untreated PCD, especially in females. Primary carnitine deficiency (PCD) affects fatty acid oxidation and is associated with cardiomyopathy and cardiac arrhythmia, but the risk of sudden death in PCD is unknown. The Faroe Islands have a high prevalence of PCD, 1:300. This study systematically investigated a possible association between untreated PCD and sudden death in young Faroese subjects. We investigated all medico-legal cases of sudden death between 1979 and 2012 among subjects below the age of 45. Stored biomaterial was examined with molecular genetic analysis to reveal PCD. We compared the prevalence of PCD among sudden death cases with that of the background population (0.23%) to calculate the odds ratio (OR) for sudden death with PCD. Biomaterial was available and genetically analyzed from 53 of 65 sudden death cases (82%) in the Faroe Islands. Six (one male and five females) of the 53 cases were homozygous for the PCD related c.95A>G mutation-a prevalence of 11.3% (95% CI 5%-23%) and an OR of 54.3 (95% CI 21-138, P < .0001) for the association between sudden death and untreated PCD. Only 11 of the 53 sudden death cases were women-of whom five were homozygous for the c.95A>G mutation (45.5%) yielding an OR of 348.8 (95% CI 94-1287, P < .0001) for the association between sudden death and untreated PCD in females. This study showed a strong association between sudden death and untreated PCD, especially in females.Primary carnitine deficiency (PCD) affects fatty acid oxidation and is associated with cardiomyopathy and cardiac arrhythmia, but the risk of sudden death in PCD is unknown. The Faroe Islands have a high prevalence of PCD, 1:300. This study systematically investigated a possible association between untreated PCD and sudden death in young Faroese subjects. We investigated all medico-legal cases of sudden death between 1979 and 2012 among subjects below the age of 45. Stored biomaterial was examined with molecular genetic analysis to reveal PCD. We compared the prevalence of PCD among sudden death cases with that of the background population (0.23%) to calculate the odds ratio (OR) for sudden death with PCD. Biomaterial was available and genetically analyzed from 53 of 65 sudden death cases (82%) in the Faroe Islands. Six (one male and five females) of the 53 cases were homozygous for the PCD related c.95A>G mutation-a prevalence of 11.3% (95% CI 5%-23%) and an OR of 54.3 (95% CI 21-138, P < .0001) for the association between sudden death and untreated PCD. Only 11 of the 53 sudden death cases were women-of whom five were homozygous for the c.95A>G mutation (45.5%) yielding an OR of 348.8 (95% CI 94-1287, P < .0001) for the association between sudden death and untreated PCD in females. This study showed a strong association between sudden death and untreated PCD, especially in females. |
Author | Joensen, Høgni D. Lund, Allan M. Rasmussen, Jan Nielsen, Olav W. Dunø, Morten Hansen, Steen‐Holger Køber, Lars Steuerwald, Ulrike |
Author_xml | – sequence: 1 givenname: Jan orcidid: 0000-0002-8650-5143 surname: Rasmussen fullname: Rasmussen, Jan email: lsjanra@ls.fo organization: Rigshospitalet University Hospital – sequence: 2 givenname: Morten surname: Dunø fullname: Dunø, Morten organization: Centre for Inherited metabolic Diseases, Copenhagen University Hospital – sequence: 3 givenname: Allan M. surname: Lund fullname: Lund, Allan M. organization: Centre for Inherited metabolic Diseases, Copenhagen University Hospital – sequence: 4 givenname: Ulrike surname: Steuerwald fullname: Steuerwald, Ulrike organization: Faroese National Health System – sequence: 5 givenname: Steen‐Holger surname: Hansen fullname: Hansen, Steen‐Holger organization: University of Copenhagen – sequence: 6 givenname: Høgni D. surname: Joensen fullname: Joensen, Høgni D. organization: Retired Chief Medical Officer – sequence: 7 givenname: Lars surname: Køber fullname: Køber, Lars organization: Rigshospitalet University Hospital – sequence: 8 givenname: Olav W. surname: Nielsen fullname: Nielsen, Olav W. organization: Bispebjerg University Hospital |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31373028$$D View this record in MEDLINE/PubMed |
BookMark | eNp9kU9rGzEQxUVIaGy3l3yAstBLCKyjkVba3WNx_jk49NKehVaapXLX2lTaJfjbR46dHELIXAaG33vMzJuSY997JOQM6BwoZZdrt7FzYCCqIzIBUfKcSSmOyYRCAXlVC3FKpjGuKaV1JcQXcsqBl5yyakLult4E1BFtFlz8l_VtFkdr0WcW9fA3cz4b_ZCIIRGPwW102GZGB-8G5zFBrTMOvdl-JSet7iJ-O_QZ-XNz_Xtxl69-3S4XP1e54aKs8kYboZvG2FoUqIVFowFKECAYlVTWnKcBArOMtVJa0AUYXtcltlA1WBR8Rs73vo-h_z9iHNTGRYNdpz32Y1SMyYoDLdKBM_LjHbrux-DTdopxWaeSfGf4_UCNzQatOhypXn-UgIs9YEIfY8D2DQGqdgGoXQDqJYAE03ewcYMeXJ-eqF33sQT2kifX4fYTc3W_fLjaa54BSCeWzw |
CitedBy_id | crossref_primary_10_1016_j_ymgme_2023_107733 crossref_primary_10_1007_s00726_023_03256_7 crossref_primary_10_1186_s13023_021_02126_3 crossref_primary_10_1016_j_heliyon_2024_e33581 crossref_primary_10_1073_pnas_2210247119 crossref_primary_10_1002_jmd2_12383 crossref_primary_10_1186_s13023_024_03267_x crossref_primary_10_3389_fped_2023_985720 crossref_primary_10_1111_ped_15404 crossref_primary_10_1111_ped_15317 crossref_primary_10_1016_j_ymgmr_2021_100776 crossref_primary_10_1002_jmd2_12319 crossref_primary_10_1111_anec_13077 crossref_primary_10_3389_fgene_2023_1304458 crossref_primary_10_1186_s13023_020_01371_2 crossref_primary_10_3390_jcm10214855 crossref_primary_10_1016_j_stemcr_2023_09_002 crossref_primary_10_1136_jmg_2023_109206 crossref_primary_10_1016_j_recesp_2023_08_013 crossref_primary_10_1186_s13052_025_01911_1 crossref_primary_10_1002_jimd_12475 crossref_primary_10_1016_j_rec_2023_08_011 crossref_primary_10_1186_s12887_020_02372_7 crossref_primary_10_1186_s13023_021_01785_6 |
Cites_doi | 10.1038/5030 10.1111/j.1399-0004.2007.00814.x 10.1016/j.ymgmr.2014.04.008 10.1002/ana.410300512 10.1159/000448321 10.1136/bmj.328.7441.702 10.1016/S0008-6363(01)00313-3 10.1159/000333127 10.1007/s10545-013-9606-2 10.1016/j.ijcard.2012.05.038 10.1038/sj.ejhg.5201578 10.1007/s10545-013-9640-0 10.1080/07315724.1998.10720458 10.1124/pr.54.4.589 10.1038/sj.ejhg.5200816 10.1007/BF03047372 10.1016/j.bbamcr.2016.01.023 10.1111/cge.12112 10.1210/jc.2018-00953 10.1073/pnas.89.14.6452 10.1007/s10545-012-9488-8 10.1007/s003950050167 10.1002/ajmg.c.30087 10.1016/S0022-3476(97)70171-9 10.1007/8904_2014_398 10.1111/j.1540-8159.2004.00507.x 10.1023/A:1005371028370 10.1196/annals.1320.007 10.1016/S0140-6736(89)92086-2 10.1007/8904_2011_52 10.1620/tjem.175.43 10.1186/1750-1172-7-68 |
ContentType | Journal Article |
Copyright | 2019 SSIEM 2019 SSIEM. Copyright © 2020 SSIEM |
Copyright_xml | – notice: 2019 SSIEM – notice: 2019 SSIEM. – notice: Copyright © 2020 SSIEM |
DBID | AAYXX CITATION NPM 7QP 7TK K9. 7X8 |
DOI | 10.1002/jimd.12158 |
DatabaseName | CrossRef PubMed Calcium & Calcified Tissue Abstracts Neurosciences Abstracts ProQuest Health & Medical Complete (Alumni) MEDLINE - Academic |
DatabaseTitle | CrossRef PubMed ProQuest Health & Medical Complete (Alumni) Calcium & Calcified Tissue Abstracts Neurosciences Abstracts MEDLINE - Academic |
DatabaseTitleList | PubMed CrossRef MEDLINE - Academic ProQuest Health & Medical Complete (Alumni) |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 1573-2665 |
EndPage | 296 |
ExternalDocumentID | 31373028 10_1002_jimd_12158 JIMD12158 |
Genre | article Journal Article |
GeographicLocations | Faroe Islands |
GeographicLocations_xml | – name: Faroe Islands |
GroupedDBID | --- -53 -5E -5G -BR -Y2 -~C .55 .86 .GJ .VR 06C 06D 0R~ 0VY 199 1N0 1OB 1OC 1SB 2.D 203 28- 29K 29~ 2J2 2JY 2KG 2KM 2LR 2P1 2VQ 2~H 30V 33P 3SX 3V. 4.4 408 409 40D 40E 53G 5GY 5QI 5RE 5VS 67Z 6NX 78A 7X7 88E 8AO 8FI 8FJ 8UJ 95- 95. 95~ 96X AAAVM AABHQ AAHHS AAHQN AAIAL AAIPD AAJKR AAMNL AANLZ AANXM AARHV AARTL AASGY AATVU AAWCG AAXRX AAYCA AAYIU AAYQN AAYTO AAYZH ABBBX ABBXA ABCUV ABHLI ABIPD ABJOX ABKTR ABMNI ABNWP ABPLI ABPPZ ABQBU ABQSL ABQWH ABTEG ABTMW ABUWG ABUWZ ACAHQ ACBXY ACCFJ ACCZN ACGFS ACHXU ACKNC ACOKC ACOMO ACPOU ACPRK ACUDM ACXBN ACXQS ADBBV ADHHG ADHIR ADIMF ADINQ ADKPE ADKYN ADMGS ADOZA ADRFC ADXAS ADZKW ADZMN AEBTG AEEZP AEFIE AEGAL AEGNC AEIGN AEJHL AEKMD AENEX AEOHA AEPYU AEQDE AETLH AEUYR AEXYK AFBBN AFEXP AFFNX AFFPM AFGKR AFKRA AFLOW AFWTZ AFWVQ AFZKB AGAYW AGGDS AGJBK AGQMX AGWIL AGWZB AGYKE AHAVH AHBTC AHBYD AHIZS AHKAY AHMBA AHSBF AHYZX AIIXL AITYG AIURR AIWBW AJBDE AJBLW AJRNO AKMHD ALIPV ALMA_UNASSIGNED_HOLDINGS ALUQN ALVPJ ALWAN AMKLP AMYDB AMYQR ARMRJ ASPBG AVWKF AZFZN B-. BA0 BBWZM BDATZ BENPR BFHJK BGNMA BPHCQ BVXVI C45 CAG CCPQU COF CS3 CSCUP D-I DCZOG DL5 DRFUL DRSTM DU5 DUUFO EBD EBS EJD EMOBN EN4 EPAXT ESBYG F5P FEDTE FIGPU FNLPD FRRFC FWDCC FYUFA G-Y G-Z GGCAI GGRSB GQ6 GQ7 GQ8 GRRUI GXS H13 HF~ HG5 HG6 HGLYW HMCUK HMJXF HQYDN HRMNR HVGLF HZ~ I09 IHE IJ- ITM IXC IZIGR IZQ I~X I~Z J-C J0Z JBSCW JCJTX KDC KOV KOW KPH LAK LATKE LEEKS LYRES M1P M4Y MA- MEWTI MXFUL MXSTM N2Q NB0 NDZJH NU0 O9- O93 O9G O9I O9J OAM OVD P19 P2P P2W P9S PF0 PQQKQ PROAC PSQYO PT5 Q2X QOK QOR QOS R4E R89 R9I RHV RNI ROL RPX RRX RSV RZC RZE RZK S16 S1Z S26 S27 S28 S37 S3B SAMSI SAP SCLPG SDE SDH SDM SHX SISQX SMD SNE SNX SOJ SPISZ SSXJD SUPJJ SV3 SZ9 SZN T13 T16 TEORI TSG TSK TSV TT1 TUC U2A U9L UG4 UKHRP VC2 W23 W48 WH7 WJK WK6 WK8 WXSBR X7M YLTOR Z45 Z7U Z7W Z82 Z87 Z8O Z8Q Z8V Z91 ZGI ZMTXR ZOVNA ZZTAW ~EX ~KM AAYXX ABFSG ABJNI ACSTC ADHKG AEYWJ AEZWR AFHIU AGHNM AGQPQ AGYGG AHWEU AIXLP CITATION PHGZM PHGZT NPM 7QP 7TK AAMMB AEFGJ AGXDD AIDQK AIDYY K9. 7X8 |
ID | FETCH-LOGICAL-c3578-bac5abbcd954ea5deca117151520606933ca1e12d22f66d1a41c3997ef18be443 |
ISSN | 0141-8955 1573-2665 |
IngestDate | Fri Sep 05 05:27:43 EDT 2025 Sat Aug 16 15:22:45 EDT 2025 Wed Feb 19 02:30:36 EST 2025 Tue Jul 01 01:55:50 EDT 2025 Thu Apr 24 23:10:26 EDT 2025 Wed Jan 22 16:34:22 EST 2025 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 2 |
Keywords | sudden death primary carnitine deficiency Faroe Islands |
Language | English |
License | 2019 SSIEM. |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c3578-bac5abbcd954ea5deca117151520606933ca1e12d22f66d1a41c3997ef18be443 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ORCID | 0000-0002-8650-5143 |
PMID | 31373028 |
PQID | 2369999634 |
PQPubID | 37420 |
PageCount | 7 |
ParticipantIDs | proquest_miscellaneous_2268310437 proquest_journals_2369999634 pubmed_primary_31373028 crossref_primary_10_1002_jimd_12158 crossref_citationtrail_10_1002_jimd_12158 wiley_primary_10_1002_jimd_12158_JIMD12158 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | March 2020 2020-03-00 2020-Mar 20200301 |
PublicationDateYYYYMMDD | 2020-03-01 |
PublicationDate_xml | – month: 03 year: 2020 text: March 2020 |
PublicationDecade | 2020 |
PublicationPlace | Hoboken, USA |
PublicationPlace_xml | – name: Hoboken, USA – name: United States – name: Dordrecht |
PublicationTitle | Journal of inherited metabolic disease |
PublicationTitleAlternate | J Inherit Metab Dis |
PublicationYear | 2020 |
Publisher | John Wiley & Sons, Inc Blackwell Publishing Ltd |
Publisher_xml | – name: John Wiley & Sons, Inc – name: Blackwell Publishing Ltd |
References | 2006; 142C 1989; 2 2004; 27 1991; 30 1997; 131 2002; 10 2006; 14 2002; 54 2018; 103 2000; 95 2016; 1863 1999; 21 2007; 72 2013; 162 1991 2014; 85 1995; 175 1998; 21 2014; 1 1998; 17 2012; 2 2013; 36 2015; 20 1984; 7 2014; 37 2004; 1033 2012; 7 1992; 89 2001; 51 2016; 68 2011; 120 e_1_2_9_30_1 e_1_2_9_31_1 e_1_2_9_11_1 e_1_2_9_10_1 e_1_2_9_13_1 e_1_2_9_32_1 e_1_2_9_12_1 e_1_2_9_33_1 e_1_2_9_15_1 e_1_2_9_14_1 e_1_2_9_17_1 e_1_2_9_16_1 e_1_2_9_19_1 e_1_2_9_18_1 e_1_2_9_20_1 e_1_2_9_22_1 e_1_2_9_21_1 e_1_2_9_24_1 e_1_2_9_23_1 e_1_2_9_8_1 e_1_2_9_7_1 e_1_2_9_6_1 e_1_2_9_5_1 e_1_2_9_4_1 e_1_2_9_3_1 e_1_2_9_2_1 e_1_2_9_9_1 e_1_2_9_26_1 e_1_2_9_25_1 e_1_2_9_28_1 e_1_2_9_27_1 e_1_2_9_29_1 |
References_xml | – volume: 142C start-page: 77 year: 2006 end-page: 85 article-title: Disorders of carnitine transport and the carnitine cycle publication-title: Am J Med Genet C Semin Med Genet – volume: 1863 start-page: 2422 year: 2016 end-page: 2435 article-title: Carnitine transport and fatty acid oxidation publication-title: Biochim Biophys Acta – volume: 175 start-page: 43 year: 1995 end-page: 53 article-title: Alteration of ammonia and carnitine levels in short‐term treatment with pivalic acid‐containing prodrug publication-title: Tohoku J Exp Med – volume: 89 start-page: 6452 year: 1992 end-page: 6456 article-title: Long‐chain fatty acids activate calcium channels in ventricular myocytes publication-title: Proc Natl Acad Sci U S A – volume: 17 start-page: 71 year: 1998 end-page: 74 article-title: Age‐and sex‐related differences of serum carnitine in a Japanese population publication-title: J Am Coll Nutr – volume: 37 start-page: 215 year: 2014 end-page: 222 article-title: Carnitine levels in 26,462 individuals from the nationwide screening program for primary carnitine deficiency in The Faroe Islands publication-title: J Inherit Metab Dis – volume: 51 start-page: 21 year: 2001 end-page: 29 article-title: Influence of L‐carnitine and its derivatives on myocardial metabolism and function in ischemic heart disease and during cardiopulmonary bypass publication-title: Cardiovasc Res – volume: 2 start-page: 469 year: 1989 end-page: 473 article-title: Carnitine deficiency induced by pivampicillin and pivmecillinam therapy publication-title: Lancet – volume: 54 start-page: 589 year: 2002 end-page: 598 article-title: Pivalate‐generating prodrugs and carnitine homeostasis in man publication-title: Pharmacol Rev – volume: 68 start-page: 5 issue: suppl 3 year: 2016 end-page: 9 article-title: Primary carnitine deficiency and newborn screening for disorders of the carnitine cycle publication-title: Ann Nutr Metab – volume: 162 start-page: e34 year: 2013 end-page: e35 article-title: Primary carnitine deficiency dilated cardiomyopathy: 28 years follow‐up publication-title: Int J Cardiol – volume: 7 start-page: 38 issue: suppl 1 year: 1984 end-page: 43 article-title: Carnitine metabolism and inborn errors publication-title: J Inherit Metab Dis – volume: 21 start-page: 428 year: 1998 end-page: 429 article-title: Dilated cardiomyopathy caused by plasma membrane carnitine transport defect publication-title: J Inherit Metab Dis – volume: 27 start-page: 675 year: 2004 end-page: 676 article-title: Ventricular fibrillation without overt cardiomyopathy as first presentation of organic cation transporter 2‐deficiency in adolescence publication-title: Pacing Clin Electrophysiol – volume: 7 start-page: 68 year: 2012 article-title: Systemic primary carnitine deficiency: an overview of clinical manifestations, diagnosis, and management publication-title: Orphanet J Rare Dis – volume: 95 start-page: 75 year: 2000 end-page: 83 article-title: Regulation by carnitine of myocardial fatty acid and carbohydrate metabolism under normal and pathological conditions publication-title: Basic Res Cardiol – volume: 85 start-page: 127 year: 2014 end-page: 137 article-title: Primary carnitine deficiency: Novel mutations and insights into the cardiac phenotype publication-title: Clin Genet – volume: 131 start-page: 304 year: 1997 end-page: 305 article-title: Sudden neonatal death in carnitine transporter deficiency publication-title: J Pediatr – volume: 36 start-page: 35 year: 2013 end-page: 41 article-title: Primary carnitine deficiency and pivalic acid exposure causing encephalopathy and fatal cardiac events publication-title: J Inherit Metab Dis – volume: 1033 start-page: 79 year: 2004 end-page: 91 article-title: Therapeutic effects of L‐carnitine and propionyl‐L‐carnitine on cardiovascular diseases: a review publication-title: Ann N Y Acad Sci – volume: 14 start-page: 497 year: 2006 end-page: 504 article-title: Highly discrepant proportions of female and male Scandinavian and British Isles ancestry within the isolated population of The Faroe Islands publication-title: Eur J Hum Genet – volume: 72 start-page: 59 year: 2007 end-page: 62 article-title: Exclusive cardiac dysfunction in familial primary carnitine deficiency cases: a genotype‐phenotype correlation publication-title: Clin Genet – volume: 120 start-page: 52 year: 2011 end-page: 58 article-title: Primary carnitine deficiency and sudden death: in vivo evidence of myocardial lipid peroxidation and sulfonylation of sarcoendoplasmic reticulum calcium ATPase 2 publication-title: Cardiology – volume: 37 start-page: 223 year: 2014 end-page: 230 article-title: Primary Carnitine deficiency in The Faroe Islands: health and cardiac status in 76 adult patients diagnosed by screening publication-title: J Inherit Metab Dis – volume: 10 start-page: 381 year: 2002 end-page: 387 article-title: Linkage disequilibrium and demographic history of the isolated population of The Faroe Islands publication-title: Eur J Hum Genet – volume: 2 start-page: 87 year: 2012 end-page: 90 article-title: Primary carnitine deficiency presents atypically with long QT syndrome: a case report publication-title: JIMD Rep – volume: 103 start-page: 4580 year: 2018 end-page: 4588 article-title: L‐Carnitine improves skeletal muscle fat oxidation in primary carnitine deficiency publication-title: J Clin Endocrinol Metab – year: 1991 – volume: 20 start-page: 103 year: 2015 end-page: 111 article-title: Carnitine levels in skeletal muscle, blood, and urine in patients with primary carnitine deficiency during intermission of L‐carnitine supplementation publication-title: JIMD Rep – volume: 21 start-page: 91 year: 1999 end-page: 94 article-title: Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion‐dependent carnitine transporter publication-title: Nat Genet – volume: 30 start-page: 709 year: 1991 end-page: 716 article-title: Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptake publication-title: Ann Neurol – volume: 1 start-page: 241 year: 2014 end-page: 248 article-title: Residual OCTN2 transporter activity, carnitine levels and symptoms correlate in patients with primary carnitine deficiency publication-title: Mol Genet Metab Rep – ident: e_1_2_9_23_1 doi: 10.1038/5030 – ident: e_1_2_9_7_1 doi: 10.1111/j.1399-0004.2007.00814.x – ident: e_1_2_9_19_1 doi: 10.1016/j.ymgmr.2014.04.008 – ident: e_1_2_9_4_1 doi: 10.1002/ana.410300512 – ident: e_1_2_9_11_1 doi: 10.1159/000448321 – ident: e_1_2_9_20_1 doi: 10.1136/bmj.328.7441.702 – ident: e_1_2_9_25_1 doi: 10.1016/S0008-6363(01)00313-3 – ident: e_1_2_9_18_1 doi: 10.1159/000333127 – ident: e_1_2_9_10_1 doi: 10.1007/s10545-013-9606-2 – ident: e_1_2_9_8_1 doi: 10.1016/j.ijcard.2012.05.038 – ident: e_1_2_9_13_1 doi: 10.1038/sj.ejhg.5201578 – ident: e_1_2_9_14_1 doi: 10.1007/s10545-013-9640-0 – ident: e_1_2_9_30_1 doi: 10.1080/07315724.1998.10720458 – ident: e_1_2_9_31_1 doi: 10.1124/pr.54.4.589 – ident: e_1_2_9_12_1 doi: 10.1038/sj.ejhg.5200816 – ident: e_1_2_9_24_1 doi: 10.1007/BF03047372 – ident: e_1_2_9_3_1 doi: 10.1016/j.bbamcr.2016.01.023 – ident: e_1_2_9_21_1 doi: 10.1111/cge.12112 – ident: e_1_2_9_29_1 doi: 10.1210/jc.2018-00953 – ident: e_1_2_9_28_1 doi: 10.1073/pnas.89.14.6452 – ident: e_1_2_9_5_1 doi: 10.1007/s10545-012-9488-8 – ident: e_1_2_9_26_1 doi: 10.1007/s003950050167 – ident: e_1_2_9_9_1 doi: 10.1002/ajmg.c.30087 – ident: e_1_2_9_16_1 doi: 10.1016/S0022-3476(97)70171-9 – ident: e_1_2_9_2_1 doi: 10.1007/8904_2014_398 – ident: e_1_2_9_15_1 doi: 10.1111/j.1540-8159.2004.00507.x – ident: e_1_2_9_6_1 doi: 10.1023/A:1005371028370 – ident: e_1_2_9_27_1 doi: 10.1196/annals.1320.007 – ident: e_1_2_9_32_1 doi: 10.1016/S0140-6736(89)92086-2 – ident: e_1_2_9_17_1 doi: 10.1007/8904_2011_52 – ident: e_1_2_9_33_1 doi: 10.1620/tjem.175.43 – ident: e_1_2_9_22_1 doi: 10.1186/1750-1172-7-68 |
SSID | ssj0009855 |
Score | 2.393837 |
Snippet | Primary carnitine deficiency (PCD) affects fatty acid oxidation and is associated with cardiomyopathy and cardiac arrhythmia, but the risk of sudden death in... |
SourceID | proquest pubmed crossref wiley |
SourceType | Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 290 |
SubjectTerms | Arrhythmia Biomaterials Cardiomyopathy Carnitine Death Faroe Islands Females Genetic analysis Health risk assessment Islands Mutation Oxidation primary carnitine deficiency Sex differences sudden death |
Title | Increased risk of sudden death in untreated primary carnitine deficiency |
URI | https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fjimd.12158 https://www.ncbi.nlm.nih.gov/pubmed/31373028 https://www.proquest.com/docview/2369999634 https://www.proquest.com/docview/2268310437 |
Volume | 43 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3db9MwELegkxAvE990DGQEL4ACteN89HGFVaVai4RaqW9RbF-kwppKbSIk_nruEjfpWEGDlyh1XTv1_XI-n-9-Zux1pDM0BIz0II2kp1IBXt8EfS_rWQVoUFjbo3znyTQczdV4ESza3JMqu6TQ783Pg3kl_yNVLEO5UpbsP0i2aRQL8B7li1eUMF5vJGN8uSmmHNoI8W1JiuSdJcOOXBllXkWSA5EB1LQShlwhBdmWFog9glIv_2ChLnNKDqQfr6BAsBAf9m8bOl_T7arcOi_OuEUa2sW0BT-IK4crBfS2oT-l82UjAPP944yhhM0P56ieX26W32HfJYHrzyYma6dFI9_Dmb_eroYDZU711gxNDmJyX4_WZ4he0-81X-y35cpWtBhxO4vtdu6nX5Lh_OIimZ0vZrfZkYzQpOqwo7PhYDBt2Zjj6jjc5pka3lr5oW37qqVybflxdTVTmSOze-zYSYmf1aC4z25B_oDdmbhIiYds1GCDEzb4OuM1NniFDb7MeYMN7rDBG2zwFhuP2Hx4Pvs48typGZ4h5iJPpyZItTa2HyhIAwsmFSIiu1X2cLXa930sACGtlFkYWpEqYdBKjSATsQal_Mesk69zeMp4mBklolBrYVIFvSyO8NW2SmirfY2fuuzNboQS4yjl6WSTy6Qmw5YJjWZSjWaXvWrqun91sNbpbqAT96JtE-mHfVqX-6rLXjZfoxqkva00h3WJdWRIR-YpHx_qSS2gphtf-DiPSWz8bSWxv_SfjD9PPlV3Jzfo6hm728L_lHWKTQnP0UYt9AuHuF9p3JQM |
linkProvider | Library Specific Holdings |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Increased+risk+of+sudden+death+in+untreated+primary+carnitine+deficiency&rft.jtitle=Journal+of+inherited+metabolic+disease&rft.au=Rasmussen%2C+Jan&rft.au=Dun%C3%B8%2C+Morten&rft.au=Lund%2C+Allan+M&rft.au=Steuerwald%2C+Ulrike&rft.date=2020-03-01&rft.issn=1573-2665&rft.eissn=1573-2665&rft.volume=43&rft.issue=2&rft.spage=290&rft_id=info:doi/10.1002%2Fjimd.12158&rft.externalDBID=NO_FULL_TEXT |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0141-8955&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0141-8955&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0141-8955&client=summon |