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DOI: 10.1055/s-2001-15976
Georg Thieme Verlag Stuttgart · New York
Lean Body Mass (LBM) als eigener Osteoporose-Risikofaktor bei postmenopausalen Frauen
Lean Body Mass as a Risk Factor for Osteoporosis in Postmenopausal WomenPublikationsverlauf
Publikationsdatum:
31. Dezember 2001 (online)
Zusammenfassung
Fragestellung
Osteoporose-Prävention mittels HRT muss mit zunehmend kritischerer Nutzen-Risiko-Diskussion gezielter indiziert werden.
Methode
Dazu wird ein Risikofaktor dargestellt, der heute leicht und kostengünstig erfahrbar ist - ohne zusätzliche Belastung der Patienten. Bei 821 postmenopausalen Frauen mit Knochendichtemessung (Bone Mineral Density [BMD] mittels DEXA-Methode) erfolgte eine Körpermasse-Analyse zur Abschätzung der fettfreien Körpermasse (Lean Body Mass [LBM] mittels bioelektrischem Impedanzverfahren).
LBM (≤ 40 kg [28 %], 40 < x ≤ 45 kg [40 %], 45 < x ≤ 50 kg [22 %], > 50 kg [10 %]) wurde mit Knochendichtewerten, Alter sowie Osteoporose-Risikofaktoren in Beziehung gebracht. Von besonderem Interesse war der Vergleich zwischen Frauen ohne HRT (n = 414) und jenen mit HRT > 5 Jahre (n = 151).
Ergebnisse
Frauen mit LBM ≤ 40 kg und ohne HRT hatten doppelt sooft „schlechte“ Knochendichte-Werte (≤ 0,8 g/cm²) als jene ohne HRT mit > 50 kg LBM: 41 % zu 19 %. Bei „guten“ BMD-Werten (> 1,0 g/cm²) war die LBM-Knochendichte-Relation umgekehrt: 11 % zu 32 %. Wurde > 5 Jahre HRT praktiziert, so hatten Frauen mit LBM ≤ 40 kg wenig häufiger „schlechte“ Knochendichte-Werte (≤ 0,8 g/cm2) als jene mit LBM > 50 kg: 17 % zu 12 %.
LBM und Alter: Beim hier erfassten postmenopausalen Kollektiv zwischen dem 45. und 80. Lebensjahr zeigten sich diesbezüglich keine signifikanten Beziehungen.
LBM unter Berücksichtigung der Fettmasse: Letztere wurde in Prozent vom Körpergewicht ermittelt: beim Quartil der „Schlanken“ (≤ 29 % Fettanteil) und beim Quartil der „Übergewichtigen“ (> 43 % Fettanteil) ergaben sich keine altersbezogenen signifikanten Zusammenhänge zu LBM.
LBM und manifeste Osteoporose: Bei Frauen ohne HRT und LBM ≤ 40 kg war Osteoporose 3-mal sooft anamnestisch bekannt als bei jenen mit > 50 kg LBM: 33 % zu 11 %. In der HRT-Gruppe war die Relation 29 % zu 19 %.
LBM und Sport/körperliche Bewegung: Die Angaben der Frauen dazu waren ohne Bezug zu den ermittelten LBM-Werten.
Schlussfolgerung
Mit Lean Body Mass (LBM) als fettfreier Körpermasse lässt sich die Muskelmasse abschätzen. Mittels bioelektrischem Impedanzverfahren gelingt dies mit geringem Zeit-/Kostenaufwand und ohne Patienten-Belastung. Bei Frauen nach der Menopause nützen LBM-Werte der Beurteilung des Osteoporose-Risikos.
Summary
Objective
We studied the lean body mass (LBM) as a potential, easily measured prognostic factor for osteoporosis.
Methods
Lean body mass was measured by bioelectrical impedance analysis and lumbar bone mineral density (BMD) with dual energy x-ray absorptiometry in 821 postmenopausal women (age 45 - 80 years). Patients were classified according to LBM (≤ 40 kg, 28 %; > 40 - ≤ 45 kg, 40 %; > 45 - ≤ 50 kg, 22 %; > 50 kg, 10 %). Contingency table analysis was performed to analyze associations between BMD, age, and risk factors for osteoporosis, particularly hormone replacement therapy (HRT). BMD values ≤ 0.8 g/cm² and > 1.0 g/cm² were classified as low and high, respectively.
Results
Among women without HRT, those with LBM ≤ 40 kg had a twice as high rate of low BMD than those with LBM > 50 (41 % vs. 19 %, respectively) and a lower rate of high BMD (11 % vs. 32 %, respectively). Among women with > 5 years of HRT, those with a LBM ≤ 40 kg had a similar rate of low BMD as those with a LBM > 50 kg (17 % and 12 %, respectively). There were no significant differences in LBM according to age. There were no age-related associations with LBM in women with a fat mass > 43 % or ≤ 29 %. A history of osteoporosis was more common in women without HRT and a LBM ≤ 40 kg than in those with a LBW > 50 kg (33 % vs. 11 %, respectively); in women with HRT the proportions were 29 % and 19 %, respectively. There was no significant correlation between LBM and physical activity.
Conclusions
Measurement of LBM is useful for estimating muscle mass. A bioelectrical impedance technique is economical in time and cost and well tolerated by patients. In postmenopausal women the LBM is helpful for evaluating the risk of osteoporosis.
Literatur
- 1 ACSM position stand on osteoporosis and exercise. Med Sci Sports Exerc. 1995; 27 1-7
- 2 Aloia J F, Vaswani A, Ma R, Flaster E. To what extent is bone mass determined by fat-free or fat mass?. Am J Clin Nutr. 1995; 61 1110-1114
- 3 Aloia J F, Vaswani A, Russo L, Sheehan M, Flaster E. The influence of menopause and hormonal replacement therapy on body cell mass and fat mass. Am J Obstet Gynecol. 1995; 172 896-900
- 4 Arden N K, Spector T D. Genetic influences on muscle strength, lean body mass and bone mineral density: a twin study. J Bone Miner Res. 1997; 12 2076-2081
- 5 Breckwoldt M. Hormonsubstitution in der Postmenopause und die Wahl des Gestagens. Geburtsh Frauenheilk. 2000; 6 279
- 6 Brincat M P. Hormon Replacement Therapy and the skin: beneficial effects: the case in favor of it. Acta Obstet Gynecol Scand. 2000; 79 244-249
- 7 Brown M, Birge S J, Kohrt W M. Hormone replacement therapy does not augment gains in muscle strength or fat-free mass in response to weight-bearing exercise. J Gerontol A Biol Sci Med Sci. 1997; 52 166-170
- 8 Castelo-Branco C, Duran M, Gonzalez-Merlo J. Skin collagen changes related to age and hormone replacement therapy. Maturitas. 1992; 15 113-119
- 9 Cauley J A, Petrini A M, LaPorte R E. The decline of grip strength in the menopause: relationship to physical activity, estrogen use and anthropometric factors. J Chronis Dis. 1987; 40 115-120
- 10 Chen Z, Lohman T G, Stini W A, Ritenbaugh Ch, Aickin M. Fat or lean tissue mass: Which one is the major determinant of bone mineral mass in healthy postmenopausal women?. J Bone Miner Res. 1997; 12 144-151
- 11 Cohn S H, Vaswani A, Zanzi I, Aloia J, Roginsky M, Ellis K J. Changes in body chemical composition with age measured by total-body neutron activation. Metabolism. 1976; 25 88-95
- 12 Compston J E, Bhambhani M, Laskey M A, Murphy S, Khaw K T. Body composition and bone mass in postmenopausal women. Clin Endocrinol. 1992; 37 426-431
- 13 Douchi T, Yamamoto S, Nakamura S, Ijuin T, Oki T, Maruta K. The effect of menopause on regional and total body lean mass. Maturitas. 1998; 17 247-252
- 14 Doyle F H, Brown J, La Chance C. Relation between bone mass and muscle weight. Lancet. 1970; 1 391
-
15 Drinkwater B L.
Physical activity, fitness and osteoporosis. Bochard C, Shepard RJ, Stephens T. Physical activity, fitness and health. International Proceedings and consensus statement. Human Kinetics 1996: 724-736 - 16 Ellis K J, Cohn S H. Correlation between bone calcium mass and muscle mass in man. J Appl Physiol. 1975; 38 455-460
- 17 Elmstahl S, Gardsell P, Ringsberg K, Sernbo I. Body composition and its relation to bone mass and fractures in an urban and a rural population. Aging. 1993; 5 47-54
- 18 Hassager C, Christiansen C. Influence of soft tissue body composition on bone mass and metabolism. Bone. 1989; 10 415-419
- 19 Hassager C, Christiansen C. Estrogen/gestagen therapy changes soft tissue body composition in postmenopausal women. Metabolism. 1989; 38 662-665
- 20 Hauner H, Berg A. Körperliche Bewegung zur Prävention und Behandlung der Adipositas. Deutsch Ärzteblatt. 2000; 97 660-665
- 21 Jackson A S, Pollock M L, Graves J E, Mahar M. Reliability and validity of bioelectrical impedance in determining body composition. J Appl Physiol. 1988; 64 529-534
- 22 Kamali P, Muller T, Lang U, Clapp J F. Cardiovascular responses of perimenopausal women to hormonal replacement therapy. Am J Obstet Gynecol. 2000; 182 17-22
- 23 Kanis J A. The menopause and the skeleton. In: Barlow DH. The menopause: key issues. Bailliere's Clin Obstet Gynaecol. 1996; 10 475-478
- 24 Khosla S, Atkinson J E, Riggs B L, Melton J L. Relationship between body composition and bone mass in women. J Bone Miner Res. 1996; 11 857-863
- 25 Kohrt W M, Ehsani A A, Birge S J. HRT preserves increases in bone mineral density and reductions in body fat after a supervised exercise program. Appl Physiol. 1998; 84 1506-1512
- 26 Kohrt W M, Snead D B, Slatopolsky E, Birge S J. Additive effects of weight-bearing exercise and estrogen on bone mineral density in older women. J Bone Miner Res. 1995; 10 1303-1311
- 27 Kristensen K, Pedersen S B, Vestergaard P, Mosekilde L, Richelsen B. Hormone replacement therapy affects body composition and leptin differently in obese and non-obese postmenopausal women. J Endocrinol. 1999; 163 55-62
- 28 Lindsay R, Cosman F, Herrington B S, Himmelstein S. Bone mass and body composition in normal women. J Bone Miner Res. 1992; 7 55-63
- 29 Longcope C H, Pratt J H, Schneider S H, Fineberg S E. Aromatization of androgens by muscle and adipose tissue in vivo. J Clin Endocrinol Metab. 1978; 46 146-151
- 30 Lübbe K, Riedel H. Transiente regionale Osteoporose in der Schwangerschaft. Geburtsh Frauenheilk. 2000; 7 380-385
- 31 Marcus R. Relationship of age-related decreases in muscle mass and strength to skeletal status. J Gerontol. 1995; 50 86-87
- 32 Marcus R, Drinkwater B, Dalsky G. Osteoporosis and exercise in women. Med Sci Sports Exerc. 1992; 24 301-307
- 33 Marone M M, Gouveia C H, Lewin S, Wehba S, Malvestiti L F, Bianco A C. Influence of body composition on the bone mass of postmenopausal women. Rev Paul Med. 1997; 115 1580-1588
- 34 Martini G, Valenti R, Giovani S, Nuit R. Age-related changes in body composition of healthy and osteoporotic women. Maturitas. 1997; 27 25-33
- 35 Martinez J A, Kearney J M, Kafatos A, Paquet S, Martinez-Gonzalez M A. Variables independently associated with selt-reported obesity in the European Union. Public Health Nutr. 1999; 2 125-133
- 36 Mautalen C, Bagur A, Vega E, Gonzalez D. Body composition in normal and osteoporotic women. Medicina (Buenos Aires). 1996; 56 29-34
- 37 Mazess R B, Barden H S. Bone density in premenopausal women: effects of age, dietary intake, physical activity, smoking and birth control pills. Am J Clin Nutr. 1991; 53 132-142
- 38 Nelson M, Mayer A B, Rutherford O, Jones D. Calcium intake, physical activity and bone mass in premenopausal women. J Human Nut Diet. 1991; 4 171-178
- 39 Orme S M, Beichetz P E. Is a low skinfold thickness an indicator for osteoporosis?. Clin Endocrinol. 1994; 41 283-287
- 40 Panotopoulos G, Raison J, Ruiz J C, Guy-Grand B, Basdevant A. Weight gain at the time of menopause. Hum Reprod. 1997; 12 126-133
- 41 Platen P. Prävention und Therapie der Osteoporose. Deutsch Ärzteblatt. 1997; 94 2097-2102
- 42 Platen P, Damm F, Marx K. Sport und Osteoporose. Dt Z Sportmed. 1995; 46 267-268
- 43 Prelevic G M, Jacobs H S. New developments in postmenopausal hormon replacement therapy. Curr Opin Obstet Gynaecol. 1997; 9 207-212
- 44 Randerath O, Kvasnicka H M, Wapniarz M. Über den Einfluß der Muskelkraft auf die Knochendichte. Osteomobiljournal. 1991; 5 12-14
- 45 Recker R R, Davies K M, Hinders S M, Heaney R P, Stegman M R, Kimmel D B. Bone gain in young adult women. JAMA. 1992; 268 2403-2408
- 46 Reid I R, Ames R, Evans M C, Sharpe S, Gamble G, France J T, Lim T MT, Cundy T. Determinantes of total body and regional bone mineral density in normal postmenopausal women - A key role for fat mass. J Clin Endocrinol Metab. 1992; 15 45-51
- 47 Snow-Harter C, Whalen R, Myburgh K, Arnaud S, Marcus R. Bone mineral density, muscle strength and recreational exercise in men. J Bone Min Res. ; 7 1291-1296
- 48 Taaffe D R, Luz Villa M, Delay R, Marcus R. Maximal muscle strength of elderly women is not influenced by oestrogen status. Age Ageing. 1995; 24 329-333
- 49 Taga M, Uemura T, Minaguchi H. The effect of hormone replacement therapy in postmenopausal women on urinary C-telopeptide and N-telopeptide of type I collagen, new markers of bone resorption. J Endocrinol Invest. 1998; 21 154-159
- 50 Takada H, Washino K, Iwata H. Risk factors for low bone mineral density among females: the effect of lean body mass. Prev Med. 1997; 26 633-638
- 51 Tekesin I, Heller S, Mayer C, Berroth R, Liebau G, Voudouri V, Sierra F, Schmidt S. Schwangerschaftskardiomyopathie in der 22. SSW. Geburtsh Frauenheilk. 2000; 7 380-385
- 52 Visser M, Kiel D P, Langlois J, Hannan M T, Felson D T, Wilson P W, Harris T B. Muscle mass and fat mass in relation to bone mineral density in very old men and women: the Framingham Heart Study. Appl Radiat Isot. 1998; 49 745-747
- 53 Wardlaw G M. Putting body weight and osteoporosis into perspective. Am J Clin Nutr. 1996; 63 433-436
- 54 Wechsler J G. Diätetische Therapie der Adipositas. Deutsch Ärzteblatt. 1997; 94 1830-1836
- 55 Wenderlein J M, Sobotha S. Osteoporoseprävention kann sich postmenopausal an Fettdepots orientieren. Frauenarzt. 2000; 41 1427-1434
Prof. Dr. J. M. Wenderlein
Universitätsfrauenklinik Ulm
Prittwitzstraße 43
89075 Ulm