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  1. Article ; Online: Negative correlation between organ heteroplasmy, particularly hepatic heteroplasmy, and age at death revealed by post-mortem studies of m.3243A > G cases.

    Yagi, Kunimasa / Okazaki, Satoko / Ohbatake, Azusa / Nakaya, Masako / Liu, Jianhui / Arite, Eiko / Miyamoto, Yukiko / Ito, Naoko / Nakano, Kaoru / Yamaaki, Naoto / Honoki, Hisae / Fujisaka, Shiho / Chujo, Daisuke / Tsunoda, Shin-Ichiro / Yanagimoto, Kunio / Nozue, Tsuyoshi / Yamada, Masayo / Ooe, Kotaro / Araki, Tsutomu /
    Nakashima, Akikatsu / Azami, Yasushi / Sodemoto, Yukio / Tadokoro, Kenichi / Nagano, Makoto / Noguchi, Tohru / Nohara, Atushi / Origasa, Hideki / Niida, Yo / Tada, Hayato

    Molecular genetics and metabolism

    2023  Volume 140, Issue 3, Page(s) 107691

    Abstract: Mitochondrial DNA m.3243A > G mutation causes mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) and its associated multi-organ disorders, including diabetes. To clarify associations between m.3243A > G organ heteroplasmy and ...

    Abstract Mitochondrial DNA m.3243A > G mutation causes mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) and its associated multi-organ disorders, including diabetes. To clarify associations between m.3243A > G organ heteroplasmy and clinical phenotypes, including the age at death, we combined genetic and pathological examinations from seven unreported and 36 literature cases of autopsied subjects. Clinical characteristics of subjects were as follows: male, 13; female, 28; unknown, 2; the age at death, 36.9 ± 20.2 [4-82] years; BMI, 16.0 ± 2.9 [13.0-22.3]; diabetes, N = 21 (49%), diabetes onset age 38.6 ± 14.2 years; deafness, N = 27 (63%); stroke-like episodes (StLEp), N = 25 (58%); congestive heart failure (CHF), N = 15 (35%); CHF onset age, 51.3 ± 14.5 years. Causes of death (N = 32) were as follows: cardiac, N = 13 (41%); infection, N = 8 (25%); StLEp, N = 4 (13%); gastrointestinal, N = 4 (13%); renal, N = 2 (6%); hepatic, N = 1 (2%). High and low heteroplasmies were confirmed in non-regenerative and regenerative organs, respectively. Heteroplasmy of the liver, spleen, leukocytes, and kidney for all subjects was significantly associated with the age at death. Furthermore, the age at death was related to juvenile-onset (any m.3243A > G-related symptoms appeared before 20) and stroke-like episodes. Multiple linear regression analysis with the age at death as an objective variable showed the significant contribution of liver heteroplasty and juvenile-onset to the age at death. m.3243A > G organ heteroplasmy levels, particularly hepatic heteroplasmy, are significantly associated with the age at death in deceased cases.
    MeSH term(s) Humans ; Male ; Female ; Adult ; Middle Aged ; Aged ; Child, Preschool ; Child ; Adolescent ; Young Adult ; Aged, 80 and over ; Heteroplasmy ; DNA, Mitochondrial/genetics ; Mutation ; Diabetes Mellitus ; Stroke/complications ; Liver/pathology ; MELAS Syndrome/genetics
    Chemical Substances DNA, Mitochondrial
    Language English
    Publishing date 2023-08-28
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1418518-0
    ISSN 1096-7206 ; 1096-7192
    ISSN (online) 1096-7206
    ISSN 1096-7192
    DOI 10.1016/j.ymgme.2023.107691
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Cutoff point separating affected and unaffected familial hypercholesterolemic patients validated by LDL-receptor gene mutants.

    Mabuchi, Hiroshi / Higashikata, Toshinori / Nohara, Atushi / Lu, Hong / Yu, Wen Xin / Nozue, Tsuyoshi / Noji, Yoshihiro / Katsuda, Shoji / Kawashiri, Masa-Aki / Inazu, Akihiro / Kobayashi, Junji / Koizumi, Junji

    Journal of atherosclerosis and thrombosis

    2005  Volume 12, Issue 1, Page(s) 35–40

    Abstract: Familial hypercholesterolemia (FH) results from low-density lipoprotein (LDL) receptor gene mutations. Heterozygotes have twice normal LDL-cholesterol concentrations in early childhood, and experience early myocardial infarction. We demonstrated bimodal ... ...

    Abstract Familial hypercholesterolemia (FH) results from low-density lipoprotein (LDL) receptor gene mutations. Heterozygotes have twice normal LDL-cholesterol concentrations in early childhood, and experience early myocardial infarction. We demonstrated bimodal cholesterol frequency distributions, independently confirming existence of an identifiable hypercholesterolemic subpopulation. We assayed blood lipids in 181 FH patients genetically diagnosed and 100 unaffected relatives. Receiver operating characteristics curves were constructed. Total cholesterol and LDL-cholesterol concentrations showed bimodality. A total cholesterol cutoff of 225 mg/dl produced results agreeing with DNA testing (specificity, 98.5%; sensitivity, 99.4%). An LDL-cholesterol cutoff of 161-163 mg/dl produced 98.5% specificity and 98.3% sensitivity. Areas under curves were 0.9826 +/- 0.0058 for total cholesterol, and 0.9852 +/- 0.0043 for LDL-cholesterol. In conclusion, we define total cholesterol and LDL-cholesterol levels of 225 and 160 mg/dl, respectively, as cutoff points of normal subjects and FH patients.
    MeSH term(s) Heterozygote ; Humans ; Hyperlipoproteinemia Type II/genetics ; Mutation ; ROC Curve ; Receptors, LDL/genetics ; Sensitivity and Specificity
    Chemical Substances Receptors, LDL
    Language English
    Publishing date 2005-02-22
    Publishing country Japan
    Document type Journal Article
    ZDB-ID 2011474-6
    ISSN 1340-3478
    ISSN 1340-3478
    DOI 10.5551/jat.12.35
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Difference in the risk factors for coronary, renal and other peripheral arteriosclerosis in heterozygous familial hypercholesterolemia.

    Yagi, Kunimasa / Hifumi, Senshu / Nohara, Atushi / Higashikata, Toshinori / Inazu, Akihiro / Mizuno, Kiyo-O / Namura, Masanobu / Ueda, Kosei / Kobayashi, Junji / Shimizu, Masami / Mabuchi, Hiroshi

    Circulation journal : official journal of the Japanese Circulation Society

    2004  Volume 68, Issue 7, Page(s) 623–627

    Abstract: Background: The aim of the present study was to clarify the risk factors of several types of arteriosclerosis lesions in Japanese individuals with heterozygous familial hypercholesterolemia (FH): renal arteriosclerosis (RAS), abdominal aortic sclerosis ( ...

    Abstract Background: The aim of the present study was to clarify the risk factors of several types of arteriosclerosis lesions in Japanese individuals with heterozygous familial hypercholesterolemia (FH): renal arteriosclerosis (RAS), abdominal aortic sclerosis (AOS), iliac arteriosclerosis (IAS) and coronary artery disease (CAD).
    Methods and results: Coronary angiography (CAG) and abdominal aortic angiography (AAA) were performed in 117 consecutive heterozygous FH subjects (79 men, 38 women; age 22-76). RAS (stenotic lesion or aneurysm) was observed in 39 cases (33%), predominantly in the proximal portion (74%) and both sides equally (right/left = 27/23). Most cases of RAS (64%) presented with <25% stenosis. The differences in the contributing risk factors for the progression and development of RAS, AOS, IAS and CAD in FH were then analyzed. Multiple logistic regression analyses showed independent risk factors for formation of atherosclerosis in each artery were: age alone for RAS; age and plasma low-density lipoprotein cholesterol (LDL-C) for AOS; age, LDL-C and high-density lipoprotein cholesterol (HDL-C) for IAS; and HDL-C and diabetes mellitus for CAD.
    Conclusion: In Japanese subjects with heterozygous FH, there are distinct risk factors for the development and progression of atherosclerosis in the renal, iliac, abdominal aorta, and coronary arteries.
    MeSH term(s) Arteriosclerosis/epidemiology ; Coronary Angiography ; Coronary Artery Disease/epidemiology ; Diabetic Angiopathies/epidemiology ; Female ; Genetic Carrier Screening ; Humans ; Hyperlipoproteinemia Type II/complications ; Hyperlipoproteinemia Type II/genetics ; Male ; Middle Aged ; Risk Factors ; Smoking ; Triglycerides/blood
    Chemical Substances Triglycerides
    Language English
    Publishing date 2004-07
    Publishing country Japan
    Document type Comparative Study ; Journal Article
    ZDB-ID 2068090-9
    ISSN 1347-4820 ; 1346-9843
    ISSN (online) 1347-4820
    ISSN 1346-9843
    DOI 10.1253/circj.68.623
    Database MEDical Literature Analysis and Retrieval System OnLINE

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