Dunnigan lipodystrophy syndrome: French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins)

被引:19
作者
Mosbah, H. [1 ,2 ]
Donadille, B. [1 ]
Vatier, C. [1 ,2 ]
Janmaat, S. [1 ,2 ]
Atlan, M. [2 ,3 ]
Badens, C. [4 ]
Barat, P. [5 ]
Beliard, S. [6 ]
Beltrand, J. [7 ]
Ben Yaou, R. [8 ]
Bismuth, E. [9 ]
Boccara, F. [10 ]
Cariou, B. [11 ]
Chaouat, M. [12 ]
Charriot, G. [13 ,14 ]
Christin-Maitre, S. [1 ,2 ,15 ]
De Kerdanet, M. [16 ]
Delemer, B. [17 ]
Disse, E. [18 ]
Dubois, N. [6 ]
Eymard, B. [8 ]
Feve, B. [1 ,2 ]
Lascols, O. [2 ,19 ]
Mathurin, P. [20 ]
Nobecourt, E. [21 ]
Poujol-Robert, A. [22 ]
Prevost, G. [23 ]
Richard, P. [24 ]
Sellam, J. [2 ,25 ]
Tauveron, I [26 ]
Treboz, D. [13 ,14 ]
Verges, B. [27 ]
Vermot-Desroches, V. [1 ]
Wahbi, K. [28 ]
Jeru, I [2 ,19 ]
Vantyghem, M. C. [29 ]
Vigouroux, C. [1 ,2 ,19 ]
机构
[1] St Antoine Univ Hosp, AP HP, Natl Reference Ctr Rare Dis Insulin Secret & Insu, Endocrinol Diabetol & Reprod Endocrinol Dept, Paris, France
[2] Sorbonne Univ, St Antoine Res Ctr, Inst Cardiometab & Nutr, Inserm UMR S938, Paris, France
[3] Tenon Hosp, AP HP, Plast Surg Dept, Paris, France
[4] AP HM, Dept Genet, Marseille, France
[5] Bordeaux Univ Hosp, Pediat Endocrinol Unit, Bordeaux, France
[6] La Concept Hosp, AP HM, Nutr Dept, Marseille, France
[7] Paris Univ, Necker Hosp, AP HP, Paediat Endocrinol Dept, Paris, France
[8] Sorbonne Univ, Pitie Salpetriere Hosp, AP HP, Myol Inst, Paris, France
[9] Paris Univ, Robert Debre Hosp, AP HP, Paediat Endocrinol Dept, Paris, France
[10] Sorbonne Univ, St Antoine Hosp, AP HP, Cardiol Dept, Paris, France
[11] Nantes Univ, Nantes Univ Hosp, Guillaume & Rene Laennec Hosp, Endocrinol Dept, Nantes, France
[12] Paris Univ, St Louis Hosp, AP HP, Plast Surg Dept, Paris, France
[13] French Lipodystrophy Assoc AFLIP, Pierrevert, France
[14] Assoc Fran Aise Lipodystrophies, Pierrevert, France
[15] Sorbonne Univ, Inserm UMR S933, Paris, France
[16] Rennes Univ Hosp, South Hosp, Paediat Endocrinol Dept, Rennes, France
[17] Reims Univ Hosp, Robert Debre Hosp, Endocrinol Dept, Reims, France
[18] Lyon Univ, Lyon Univ Hosp, South Lyon Civil Hosp, Endocrinol Dept, Pierre Benite, France
[19] St Antoine Univ Hosp, AP HP, Mol Biol & Genet Dept, Paris, France
[20] Lille Univ, Lille 2 Univ Hosp, Hepatol Dept, Lille, France
[21] Reunion South Hosp, La Reunion Univ Hosp, Endocrinol Dept, St Pierre La Reunion, France
[22] Sorbonne Univ, St Antoine Hosp, AP HP, Hepatol Dept, Paris, France
[23] Bois Guillaume Hosp, Rouen Univ Hosp, Endocrinol Dept, Rouen, France
[24] Sorbonne Univ, Pitie Salpetriere Hosp, AP HP, Cardiogenet & Myogenet Dept, Paris, France
[25] Sorbonne Univ, St Antoine Hosp, AP HP, Rhumatol Dept, Paris, France
[26] Clermont Auvergne Univ, Clermont Ferrand Univ Hosp, Endocrinol Dept, Clermont Ferrand, France
[27] Bourgogne Univ, Dijon Univ Hosp, Francois Mitterand Hosp, Endocrinol Diabetol Dept, Dijon, France
[28] Paris Univ, Cochin Hosp, AP HP, Cardiol Dept, Paris, France
[29] Lille Univ, Lille 2 Univ Hosp, Endocrinol Dept, Lille, France
关键词
Type 2 familial partial lipodystrophy; Dunnigan syndrome; Dunnigan disease; Insulin-resistant diabetes; Diagnosis; Recommendation; Management; FAMILIAL PARTIAL LIPODYSTROPHY; LONG-TERM TREATMENT; ENCODING LAMIN A/C; HEPATIC STEATOSIS; LMNA; MANAGEMENT; WOMEN; METRELEPTIN; PREVALENCE; GUIDELINES;
D O I
10.1186/s13023-022-02308-7
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Dunnigan syndrome, or Familial Partial Lipodystrophy type 2 (FPLD2; ORPHA 2348), is a rare autosomal dominant disorder due to pathogenic variants of the LMNA gene. The objective of the French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins), is to provide health professionals with a guide to optimal management and care of patients with FPLD2, based on a critical literature review and multidisciplinary expert consensus. The PNDS, written by members of the French National Reference Center for Rare Diseases of Insulin Secretion and Insulin Sensitivity (PRISIS), is available on the French Health Authority website (in French). Dunnigan syndrome is characterized by a partial atrophy of the subcutaneous adipose tissue and by an insulin resistance syndrome, associated with a risk of metabolic, cardiovascular and muscular complications. Its prevalence, assessed at 1/100.000 in Europe, is probably considerably underestimated. Thorough clinical examination is key to diagnosis. Biochemical testing frequently shows hyperinsulinemia, abnormal glucose tolerance and hypertriglyceridemia. Elevated hepatic transaminases (hepatic steatosis) and creatine phosphokinase, and hyperandrogenism in women, are common. Molecular analysis of the LMNA gene confirms diagnosis and allows for family investigations. Regular screening and multidisciplinary monitoring of the associated complications are necessary. Diabetes frequently develops from puberty onwards. Hypertriglyceridemia may lead to acute pancreatitis. Early atherosclerosis and cardiomyopathy should be monitored. In women, polycystic ovary syndrome is common. Overall, the management of patients with Dunnigan syndrome requires the collaboration of several health care providers. The attending physician, in conjunction with the national care network, will ensure that the patient receives optimal care through regular follow-up and screening. The various elements of this PNDS are described to provide such a support.
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