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  1. Article ; Online: Presentation of the 2019 SSCI Founders' Medal Award.

    Lee Hamm, L

    The American journal of the medical sciences

    2019  Volume 358, Issue 1, Page(s) 62

    MeSH term(s) Awards and Prizes ; Clinical Medicine/history ; History, 21st Century ; Humans ; Societies, Medical/history ; United States
    Language English
    Publishing date 2019-05-07
    Publishing country United States
    Document type Editorial ; Historical Article
    ZDB-ID 82078-7
    ISSN 1538-2990 ; 0002-9629
    ISSN (online) 1538-2990
    ISSN 0002-9629
    DOI 10.1016/j.amjms.2019.04.021
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Book: Acid base and electrolyte disorders

    Dubose, Thomas D. / Hamm, L. Lee

    a companion to Brenner & Rector's The kidney

    2002  

    Title variant Acid-base and electrolyte disorders
    Author's details Thomas D. DuBose ; L. Lee Hamm
    Keywords Kidney Diseases ; Kidney / physiopathology ; Acid-Base Imbalance ; Water-Electrolyte Imbalance
    Language English
    Size XVI, 547 S. : zahlr. Ill., graph. Darst.
    Publisher Saunders
    Publishing place Philadelphia u.a.
    Publishing country United States
    Document type Book
    HBZ-ID HT013463236
    ISBN 0-7216-8956-6 ; 978-0-7216-8956-2
    Database Catalogue ZB MED Medicine, Health

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  3. Article: Acidosis and citrate: provocative interactions.

    Hering-Smith, Kathleen S / Hamm, L Lee

    Annals of translational medicine

    2018  Volume 6, Issue 18, Page(s) 374

    Language English
    Publishing date 2018-10-12
    Publishing country China
    Document type Editorial ; Comment
    ZDB-ID 2893931-1
    ISSN 2305-5847 ; 2305-5839
    ISSN (online) 2305-5847
    ISSN 2305-5839
    DOI 10.21037/atm.2018.07.37
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Regulation of Acid-Base Balance in Chronic Kidney Disease.

    Nagami, Glenn T / Hamm, L Lee

    Advances in chronic kidney disease

    2017  Volume 24, Issue 5, Page(s) 274–279

    Abstract: ... to give bicarbonate supplementation in CKD is reserved for those with a bicarbonate level of 22 mEq/L ... mEq/L. ...

    Abstract The kidneys play a major role in the regulation of acid-base balance by reabsorbing bicarbonate filtered by the glomeruli and excreting titratable acids and ammonia into the urine. In CKD, with declining kidney function, acid retention and metabolic acidosis occur, but the extent of acid retention depends not only on the degree of kidney impairment but also on the dietary acid load. Acid retention can occur even when the serum bicarbonate level is apparently normal. With reduced kidney function, acid transport processes in the surviving nephrons are augmented but as disease progresses ammonia excretion and, in some individuals, the ability to reabsorb bicarbonate falls, whereas titratable acid excretion is preserved until kidney function is severely impaired. Urinary ammonia levels are used to gauge the renal response to acid loads and are best assessed by direct measurement of urinary ammonia levels rather than by indirect assessments. In individuals with acidosis from CKD, an inappropriately low degree of ammonia excretion points to the pathogenic role of impaired urinary acid excretion. The presence of a normal bicarbonate level in CKD complicates the interpretation of the urinary ammonia excretion as such individuals could be in acid-base balance or could be retaining acid without manifesting a low bicarbonate level. At this time, the decision to give bicarbonate supplementation in CKD is reserved for those with a bicarbonate level of 22 mEq/L, but because of potential harm of overtreatment, supplementation should be adjusted to maintain a bicarbonate level of <26 mEq/L.
    Language English
    Publishing date 2017
    Publishing country United States
    Document type Journal Article ; Review ; Research Support, Non-U.S. Gov't
    ISSN 1548-5609 ; 1548-5595
    ISSN (online) 1548-5609
    ISSN 1548-5595
    DOI 10.1053/j.ackd.2017.07.004
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Trends in Cardiovascular Risk Factors in US Adults by Race and Ethnicity and Socioeconomic Status, 1999-2018.

    He, Jiang / Zhu, Zhengbao / Bundy, Joshua D / Dorans, Kirsten S / Chen, Jing / Hamm, L Lee

    JAMA

    2021  Volume 326, Issue 13, Page(s) 1286–1298

    Abstract: Importance: After decades of decline, the US cardiovascular disease mortality rate flattened after 2010, and racial and ethnic differences in cardiovascular disease mortality persisted.: Objective: To examine 20-year trends in cardiovascular risk ... ...

    Abstract Importance: After decades of decline, the US cardiovascular disease mortality rate flattened after 2010, and racial and ethnic differences in cardiovascular disease mortality persisted.
    Objective: To examine 20-year trends in cardiovascular risk factors in the US population by race and ethnicity and by socioeconomic status.
    Design, setting, and participants: A total of 50 571 participants aged 20 years or older from the 1999-2018 National Health and Nutrition Examination Surveys, a series of cross-sectional surveys in nationally representative samples of the US population, were included.
    Exposures: Calendar year, race and ethnicity, education, and family income.
    Main outcomes and measures: Age- and sex-adjusted means or proportions of cardiovascular risk factors and estimated 10-year risk of atherosclerotic cardiovascular disease were calculated for each of 10 two-year cycles.
    Results: The mean age of participants ranged from 49.0 to 51.8 years and the proportion of women from 48.2% to 51.3% in the surveys. From 1999-2000 to 2017-2018, age- and sex-adjusted mean body mass index increased from 28.0 (95% CI, 27.5-28.5) to 29.8 (95% CI, 29.2-30.4); mean hemoglobin A1c increased from 5.4% (95% CI, 5.3%-5.5%) to 5.7% (95% CI, 5.6%-5.7%) (both P < .001 for linear trends). Mean serum total cholesterol decreased from 203.3 mg/dL (95% CI, 200.9-205.8 mg/dL) to 188.5 mg/dL (95% CI, 185.2-191.9 mg/dL); prevalence of smoking decreased from 24.8% (95% CI, 21.8%-27.7%) to 18.1% (95% CI, 15.4%-20.8%) (both P < .001 for linear trends). Mean systolic blood pressure decreased from 123.5 mm Hg (95% CI, 122.2-124.8 mm Hg) in 1999-2000 to 120.5 mm Hg (95% CI, 119.6-121.3 mm Hg) in 2009-2010, then increased to 122.8 mm Hg (95% CI, 121.7-123.8 mm Hg) in 2017-2018 (P < .001 for nonlinear trend). Age- and sex-adjusted 10-year atherosclerotic cardiovascular disease risk decreased from 7.6% (95% CI, 6.9%-8.2%) in 1999-2000 to 6.5% (95% CI, 6.1%-6.8%) in 2011-2012, then did not significantly change. Age- and sex-adjusted body mass index, systolic blood pressure, and hemoglobin A1c were consistently higher, while total cholesterol was lower in non-Hispanic Black participants compared with non-Hispanic White participants (all P < .001 for group differences). Individuals with college or higher education or high family income had consistently lower levels of cardiovascular risk factors. The mean age- and sex-adjusted 10-year risk of atherosclerotic cardiovascular disease was significantly higher in non-Hispanic Black participants compared with non-Hispanic White participants (difference, 1.4% [95% CI, 1.0%-1.7%] in 1999-2008 and 2.0% [95% CI, 1.7%-2.4%] in 2009-2018]). This difference was attenuated (-0.3% [95% CI, -0.6% to 0.1%] in 1999-2008 and 0.7% [95% CI, 0.3%-1.0%] in 2009-2018) after further adjusting for education, income, home ownership, employment, health insurance, and access to health care.
    Conclusions and relevance: In this serial cross-sectional survey study that estimated US trends in cardiovascular risk factors from 1999 through 2018, differences in cardiovascular risk factors persisted between Black and White participants; the difference may have been moderated by social determinants of health.
    MeSH term(s) Adult ; Age Factors ; Aged ; Atherosclerosis/epidemiology ; Blood Pressure ; Body Mass Index ; Cardiovascular Diseases/ethnology ; Cardiovascular Diseases/mortality ; Cholesterol/blood ; Confidence Intervals ; Cross-Sectional Studies ; Educational Status ; Ethnicity ; Female ; Glycated Hemoglobin A/analysis ; Heart Disease Risk Factors ; Humans ; Income/trends ; Linear Models ; Male ; Middle Aged ; Nutrition Surveys/trends ; Prevalence ; Racial Groups/ethnology ; Sex Factors ; Smoking/epidemiology ; Smoking/trends ; Social Class ; Social Determinants of Health/ethnology ; Social Determinants of Health/trends ; Time Factors ; United States/ethnology ; Young Adult
    Chemical Substances Glycated Hemoglobin A ; Cholesterol (97C5T2UQ7J)
    Language English
    Publishing date 2021-11-12
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 2958-0
    ISSN 1538-3598 ; 0254-9077 ; 0002-9955 ; 0098-7484
    ISSN (online) 1538-3598
    ISSN 0254-9077 ; 0002-9955 ; 0098-7484
    DOI 10.1001/jama.2021.15187
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Effects of chronic hypercapnia on ammonium transport in the mouse kidney.

    Abdulnour-Nakhoul, Solange / Hering-Smith, Kathleen / Hamm, L Lee / Nakhoul, Nazih L

    Physiological reports

    2019  Volume 7, Issue 16, Page(s) e14221

    Abstract: Hypercapnia and subsequent respiratory acidosis are serious complications in many patients with respiratory disorders. The acute response to hypercapnia is buffering of ... ...

    Abstract Hypercapnia and subsequent respiratory acidosis are serious complications in many patients with respiratory disorders. The acute response to hypercapnia is buffering of H
    MeSH term(s) Acidosis, Respiratory/etiology ; Acidosis, Respiratory/metabolism ; Ammonium Compounds/metabolism ; Animals ; Cation Transport Proteins/metabolism ; Hypercapnia/complications ; Hypercapnia/metabolism ; Kidney Tubules, Collecting/metabolism ; Membrane Glycoproteins/metabolism ; Mice
    Chemical Substances Ammonium Compounds ; Cation Transport Proteins ; Membrane Glycoproteins ; Rh type B glycoprotein, rat ; Rh type C glycoprotein, rat
    Language English
    Publishing date 2019-08-27
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 2724325-4
    ISSN 2051-817X ; 2051-817X
    ISSN (online) 2051-817X
    ISSN 2051-817X
    DOI 10.14814/phy2.14221
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: The role of bicarbonate in CKD: evidence bulks up.

    Simon, Eric E / Hamm, L Lee

    Clinical journal of the American Society of Nephrology : CJASN

    2013  Volume 8, Issue 5, Page(s) 703–705

    MeSH term(s) Acidosis/drug therapy ; Female ; Humans ; Male ; Renal Insufficiency, Chronic/drug therapy ; Sodium Bicarbonate/administration & dosage
    Chemical Substances Sodium Bicarbonate (8MDF5V39QO)
    Language English
    Publishing date 2013-04-25
    Publishing country United States
    Document type Editorial ; Comment
    ZDB-ID 2226665-3
    ISSN 1555-905X ; 1555-9041
    ISSN (online) 1555-905X
    ISSN 1555-9041
    DOI 10.2215/CJN.03190313
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Excess risk of cardiovascular events in patients in the United States vs. Japan with chronic kidney disease is mediated mainly by left ventricular structure and function.

    Imaizumi, Takahiro / Fujii, Naohiko / Hamano, Takayuki / Yang, Wei / Taguri, Masataka / Kansal, Mayank / Mehta, Rupal / Shafi, Tariq / Taliercio, Jonathan / Go, Alan / Rao, Panduranga / Hamm, L Lee / Deo, Rajat / Maruyama, Shoichi / Fukagawa, Masafumi / Feldman, Harold I

    Kidney international

    2023  Volume 103, Issue 5, Page(s) 949–961

    Abstract: While patients receiving dialysis therapy in the United States are more likely to develop cardiovascular disease (CVD) than those in Japan, direct comparisons of patients with predialysis chronic kidney disease (CKD) are rare. To study this, we compared ... ...

    Abstract While patients receiving dialysis therapy in the United States are more likely to develop cardiovascular disease (CVD) than those in Japan, direct comparisons of patients with predialysis chronic kidney disease (CKD) are rare. To study this, we compared various outcomes in patients with predialysis CKD using data from the Chronic Renal Insufficiency Cohort (CRIC) and CKD Japan Cohort (CKD-JAC) studies and determined mediators of any differences. Candidate mediators included left ventricular (LV) indices assessed by echocardiography. Among 3125 CRIC and 1097 CKD-JAC participants, the mean LV mass index (LVMI) and ejection fraction (EF) were 55.7 and 46.6 g/m
    MeSH term(s) Humans ; United States/epidemiology ; Japan/epidemiology ; C-Reactive Protein ; Risk Factors ; Renal Insufficiency, Chronic/complications ; Renal Insufficiency, Chronic/diagnosis ; Renal Insufficiency, Chronic/epidemiology ; Cardiovascular Diseases/diagnosis ; Cardiovascular Diseases/epidemiology ; Cardiovascular Diseases/etiology ; Hypertrophy, Left Ventricular/diagnostic imaging ; Hypertrophy, Left Ventricular/epidemiology ; Hypertrophy, Left Ventricular/etiology
    Chemical Substances C-Reactive Protein (9007-41-4)
    Language English
    Publishing date 2023-02-02
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 120573-0
    ISSN 1523-1755 ; 0085-2538
    ISSN (online) 1523-1755
    ISSN 0085-2538
    DOI 10.1016/j.kint.2023.01.008
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article: Personal observations and lessons from Katrina.

    Hamm, L Lee

    The American journal of the medical sciences

    2006  Volume 332, Issue 5, Page(s) 245–250

    MeSH term(s) Community Health Services/organization & administration ; Delivery of Health Care ; Disaster Planning/methods ; Disasters ; Emergencies ; Humans ; Louisiana ; Public Health Administration ; Relief Work ; Rescue Work/methods
    Language English
    Publishing date 2006-09-05
    Publishing country United States
    Document type Journal Article
    ZDB-ID 82078-7
    ISSN 1538-2990 ; 0002-9629
    ISSN (online) 1538-2990
    ISSN 0002-9629
    DOI 10.1097/00000441-200611000-00014
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Association of Mitochondrial DNA Copy Number with Risk of Progression of Kidney Disease.

    He, William J / Li, Changwei / Huang, Zhijie / Geng, Siyi / Rao, Varun S / Kelly, Tanika N / Hamm, L Lee / Grams, Morgan E / Arking, Dan E / Appel, Lawrence J / Rebholz, Casey M

    Clinical journal of the American Society of Nephrology : CJASN

    2022  Volume 17, Issue 7, Page(s) 966–975

    Abstract: Background and objectives: Mitochondrial DNA copy number is a biomarker of mitochondrial function, which has been hypothesized to contribute to pathogenesis of CKD through podocyte injury, tubular epithelial cell damage, and endothelial dysfunction. The ...

    Abstract Background and objectives: Mitochondrial DNA copy number is a biomarker of mitochondrial function, which has been hypothesized to contribute to pathogenesis of CKD through podocyte injury, tubular epithelial cell damage, and endothelial dysfunction. The prospective association of mitochondrial DNA copy number with CKD progression has not been previously evaluated.
    Design, setting, participants, & measurements: Chronic Renal Insufficiency Cohort study participants had serum levels of mitochondrial DNA copy number calculated from probe intensities of mitochondrial single nucleotide polymorphisms genotyped on the Illumina HumanOmni 1-Quad Array. CKD progression was defined as kidney failure or halving of eGFR from baseline. Cox proportional hazards models were used to calculate hazard ratios for mitochondrial DNA copy number and risk of CKD progression.
    Results: Among 2943 participants, mean age was 58 years, 45% were women, and 48% self-identified as Black. There were 1077 patients who experienced CKD progression over a median follow-up of 6.5 years. The incidence rate of CKD progression was highest for those in the lowest tertile of mitochondrial DNA copy number (tertile 1, 58.1; tertile 2, 50.8; tertile 3, 46.3 per 1000 person-years). Risk for CKD progression was higher for participants with lower levels of mitochondrial DNA copy number after adjustment for established risk factors (for tertile 1 versus 3, hazard ratio, 1.28 [95% confidence interval, 1.10 to 1.50]; for tertile 2 versus 3, hazard ratio, 0.99 [95% confidence interval, 0.85 to 1.16]; trend
    Conclusions: These findings suggest lower mitochondrial DNA copy number is associated with higher risk of CKD progression, independent of established risk factors among patients with CKD.
    MeSH term(s) Albuminuria/epidemiology ; Albuminuria/genetics ; Cohort Studies ; DNA Copy Number Variations ; DNA, Mitochondrial/genetics ; Disease Progression ; Female ; Glomerular Filtration Rate ; Humans ; Male ; Middle Aged ; Mitochondria ; Prospective Studies ; Renal Insufficiency, Chronic/epidemiology ; Renal Insufficiency, Chronic/genetics ; Risk Factors
    Chemical Substances DNA, Mitochondrial
    Language English
    Publishing date 2022-06-07
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2226665-3
    ISSN 1555-905X ; 1555-9041
    ISSN (online) 1555-905X
    ISSN 1555-9041
    DOI 10.2215/CJN.15551121
    Database MEDical Literature Analysis and Retrieval System OnLINE

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