Evidence map›Paper›PMID 29607946›Full record

ArticleInternal medicine (Tokyo, Japan)2018

Clinical Characteristics, Phenotype of Lipodystrophy and a Genetic Analysis of Six Diabetic Japanese Women with Familial Partial Lipodystrophy in a Diabetic Outpatient Clinic.

Masanori Iwanishi, Jun Ito-Kobayashi, Miki Washiyama, Toru Kusakabe, Ken Ebihara

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Article in Internal medicine (Tokyo, Japan), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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2 citing papers in PubMed.

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5 · Who and what money

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5 authors.

Masanori IwanishiDepartment of Diabetes and Endocrinology, Kusatsu General Hospital, Japan.
Jun Ito-KobayashiDepartment of Diabetes and Endocrinology, Kusatsu General Hospital, Japan.
Miki WashiyamaDepartment of Diabetes and Endocrinology, Kusatsu General Hospital, Japan.
Toru KusakabeDepartment of Endocrinology, Metabolism and Hypertension, Clinical Research Institute, National Hospital Organization Kyoto Medical Center, Japan.
Ken EbiharaDivision of Endocrinology and Metabolism, Jichi Medical University, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective Our aim was to examine the clinical characteristics and phenotype of lipodystrophy of six diabetic Japanese women with partial lipodystrophy (PL) who received a genetic analysis at a diabetic outpatient clinic. Methods We screened for PL using dual energy X-ray absorptiometry (DEXA) and magnetic resonance imaging (MRI) among patients who had a reduced peripheral skinfold thickness at the diabetic outpatient clinic of Kusatsu General Hospital between August 2003 and August 2013. We performed a mutation analysis of candidate genes, including LMNA and PPARG, in two patients with PL and whole-exome sequencing in four patients with PL. Results We identified 15 patients with PL and performed a genetic analysis in 6 of them. They had no mutations in candidate genes known to be associated with familial partial lipodystrophy (FPLD). They all had near-complete loss of subcutaneous fat, particularly in the antero-lateral and posterior thigh region and the calf region. As almost all patients were characterized by fat loss in the lower limbs with abdominal fat accumulation, a high rate of positivity for a family history, diabetes, and an unknown genetic cause, we suspected they might have FPLD1. Some patients have shown relatively severe insulin resistance, while others have shown insulin deficiency. Four and one had severe atherosclerosis and liver cirrhosis, probably due to nonalcoholic steatohepatitis, respectively. Conclusion Almost all patients with PL identified in a diabetic outpatient clinic had subcutaneous fat loss in the lower limbs with excess truncal fat and might have had FPLD1.

Indexed as

Absorptiometry, PhotonAgedAmbulatory Care FacilitiesAsian PeopleDiabetes ComplicationsFemaleGenetic TestingHumansJapanLamin Type ALipodystrophy, Familial PartialMiddle AgedMutationPhenotypePPAR gammaSkinfold ThicknessLamin Type ALMNA protein, humanPPAR gammadiabetic outpatient clinicfamilial partial lipodystrophy (FPLD)partial lipodystrophy (PL)

Identifiers

PMID29607946
PMCPMC6148158

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.